Publications
Title | Abstract | Year(sorted descending) Filter | PMID Filter |
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enhanced poly(3-hydroxypropionate) production via β-alanine pathway in recombinant escherichia coli. | poly(3-hydroxypropionate) (p3hp) is a thermoplastic with great compostability and biocompatibility, and can be produced through several biosynthetic pathways, in which the glycerol pathway achieved the highest p3hp production. however, exogenous supply of vitamin b12 was required to maintain the activity of glycerol dehydratase, resulting in high production cost. to avoid the addition of vb12, we have previously constructed a p3hp biosynthetic route with β-alanine as intermediate, and the presen ... | 2017 | 28253372 |
bacterial genome editing via a designed toxin-antitoxin cassette. | manipulating the bacterial genomes in an efficient manner is essential to biological and biotechnological research. here, we reprogrammed the bacterial ta systems as the toxin counter-selectable cassette regulated by an antitoxin switch (tccras) for genetic modifications in the extensively studied and utilized gram-positive bacteria, b. subtilis and corynebacterium glutamicum. in the five characterized type ii ta systems, the relbe complex can specifically and efficiently regulate cell growth an ... | 2017 | 28094982 |
inactivation of genes involved in base excision repair of corynebacterium glutamicum and survival of the mutants in presence of various mutagens. | base excision repair (ber) is considered as the most active dna repair pathway in vivo, which is initiated by recognition of the nucleotide lesions and excision of the damaged dna base. the genome of corynebacterium glutamicum atcc 13032 contains various dna glycosylases encoding genes (ung, fpg/mutm, tagi, alka, muty), two ap-endonuclease encoding genes (nei and nth) and an exonuclease encoding gene xth. to investigate the role of these genes during dna repair in c. glutamicum, mutants with del ... | 2017 | 28391506 |
heterologous expression of the halothiobacillus neapolitanus carboxysomal gene cluster in corynebacterium glutamicum. | compartmentalization represents a ubiquitous principle used by living organisms to optimize metabolic flux and to avoid detrimental interactions within the cytoplasm. proteinaceous bacterial microcompartments (bmcs) have therefore created strong interest for the encapsulation of heterologous pathways in microbial model organisms. however, attempts were so far mostly restricted to escherichia coli. here, we introduced the carboxysomal gene cluster of halothiobacillus neapolitanus into the biotech ... | 2017 | 28359868 |
redirecting carbon flux through pgi-deficient and heterologous transhydrogenase toward efficient succinate production in corynebacterium glutamicum. | corynebacterium glutamicum is particularly known for its potentiality in succinate production. we engineered c. glutamicum for the production of succinate. to enhance c3-c4 carboxylation efficiency, chromosomal integration of the pyruvate carboxylase gene pyc resulted in strain nc-4. to increase intracellular nadh pools, the pntab gene from escherichia coli, encoding for transhydrogenase, was chromosomally integrated into nc-4, leading to strain nc-5. furthermore, we deleted pgi gene in strain n ... | 2017 | 28303352 |
functional expression of plant-derived o-methyltransferase, flavanone 3-hydroxylase, and flavonol synthase in corynebacterium glutamicum for production of pterostilbene, kaempferol, and quercetin. | plant polyphenols receive significant attention due to their anti-oxidative and health-promoting properties, and several microorganisms are currently engineered towards producing these valuable compounds. previously, corynebacterium glutamicum has been engineered for synthesizing polyphenol core structures such as the stilbene resveratrol and the (2s)-flavanone naringenin. decoration of these compounds by o-methylation or hydroxylation would provide access to polyphenols of even higher commercia ... | 2017 | 28143765 |
heat-killed cell preparation of corynebacterium glutamicum stimulates the immune activity and improves survival of mice against enterohemorrhagic escherichia coli. | fermentation by corynebacterium glutamicum is used by various industries to produce l-glutamate, and the heat-killed cell preparation of this bacterium (hccg) is a by-product of the fermentation process. in present study, we evaluated the immunostimulating and survival effects against enterohemorrhagic escherichia coli (stec) infection of hccg. hccg significantly stimulated in vitro iga and interleukin-12 p70 production in murine peyer's patch cells and peritoneal macrophages, respectively. oral ... | 2017 | 28137189 |
biotin-independent strains of escherichia coli for enhanced streptavidin production. | biotin is an archetypal vitamin used as cofactor for carboxylation reactions found in all forms of life. however, biotin biosynthesis is an elaborate multi-enzymatic process and metabolically costly. moreover, many industrially relevant organisms are incapable of biotin synthesis resulting in the requirement to supplement defined media. here we describe the creation of biotin-independent strains of escherichia coli and corynebacterium glutamicum through installation of an optimized malonyl-coa b ... | 2017 | 28062280 |
polynucleotide phosphorylase, rnase e/g, and ybey are involved in the maturation of 4.5s rna in corynebacterium glutamicum. | corynebacterium glutamicum has been applied for the industrial production of various metabolites, such as amino acids. to understand the biosynthesis of the membrane protein in this bacterium, we investigated the process of signal recognition particle (srp) assembly. srp is found in all three domains of life and plays an important role in the membrane insertion of proteins. srp rna is initially transcribed as precursor molecules; however, relatively little is known about its maturation. in c. gl ... | 2017 | 28031281 |
comparing galactan biosynthesis in mycobacterium tuberculosis and corynebacterium diphtheriae. | the suborder corynebacterineae encompasses species like corynebacterium glutamicum, which has been harnessed for industrial production of amino acids, as well as corynebacterium diphtheriae and mycobacterium tuberculosis, which cause devastating human diseases. a distinctive component of the corynebacterineae cell envelope is the mycolyl-arabinogalactan (mag) complex. the mag is composed of lipid mycolic acids, and arabinofuranose (araf) and galactofuranose (galf) carbohydrate residues. elucidat ... | 2017 | 28039359 |
metabolic engineering of corynebacterium glutamicum for the production of 3-hydroxypropionic acid from glucose and xylose. | 3-hydroxypropionic acid (3-hp) is a promising platform chemical which can be used for the production of various value-added chemicals. in this study,corynebacterium glutamicum was metabolically engineered to efficiently produce 3-hp from glucose and xylose via the glycerol pathway. a functional 3-hp synthesis pathway was engineered through a combination of genes involved in glycerol synthesis (fusion of gpd and gpp from saccharomyces cerevisiae) and 3-hp production (pducdegh from klebsiella pneu ... | 2017 | 27918882 |
heme derived from corynebacterium glutamicum: a potential iron additive for swine and an electron carrier additive for lactic acid bacterial culture. | to investigate the potential applications of bacterial heme, aminolevulinic acid synthase (hema) was expressed in a corynebacterium glutamicum ha strain that had been adaptively evolved against oxidative stress. the red pigment from the constructed strain was extracted and it exhibited the typical heme absorbance at 408 nm from the spectrum. to investigate the potential of this strain as an iron additive for swine, a prototype feed additive was manufactured in pilot scale by culturing the strain ... | 2017 | 28035120 |
the antituberculosis drug ethambutol selectively blocks apical growth in cmn group bacteria. | members of the genus mycobacterium are the most prevalent cause of infectious diseases. mycobacteria have a complex cell envelope containing a peptidoglycan layer and an additional arabinogalactan polymer to which a mycolic acid bilayer is linked; this complex, multilayered cell wall composition (magp) is conserved among all cmn group bacteria. the arabinogalactan and mycolic acid synthesis pathways constitute effective drug targets for tuberculosis treatment. ethambutol (emb), a classical antit ... | 2017 | 28174310 |
identification of a membrane protein required for lipomannan maturation and lipoarabinomannan synthesis in corynebacterineae. | mycobacterium tuberculosis and related corynebacterineae synthesize a family of lipomannans (lm) and lipoarabinomannans (lam) that are abundant components of the multilaminate cell wall and essential virulence factors in pathogenic species. here we describe a new membrane protein, highly conserved in all corynebacterineae, that is required for synthesis of full-length lm and lam. deletion of the corynebacterium glutamicum ncgl2760 gene resulted in a complete loss of mature lm/lam and the appeara ... | 2017 | 28167532 |
sequence-based identification of inositol monophosphatase-like histidinol-phosphate phosphatases (hisn) in corynebacterium glutamicum, actinobacteria, and beyond. | the eighth step of l-histidine biosynthesis is carried out by an enzyme called histidinol-phosphate phosphatase (holpase). three unrelated holpase families are known so far. two of them are well studied: had-type holpases known from gammaproteobacteria like escherichia coli or salmonella enterica and php-type holpases known from yeast and firmicutes like bacillus subtilis. however, the third family of holpases, the inositol monophosphatase (impase)-like holpases, present in actinobacteria like c ... | 2017 | 28720084 |
a truncated sph12-38 with potent antimicrobial activity showing resistance against bacterial challenge in oryzias melastigma. | antimicrobial peptides (amps) represent an efficient part of innate immunity and are found in a variety of life. among them histone 2a (h2a), as a promising class of amps, attracts great attention, but the in vivo mechanism of h2a derived amp is still less known. based on the acquisition of sphistin, a synthetic 38-amino acid h2a derived peptide from scylla paramamosain, as reported in our previous study, was truncated into three short fragments (sph12-38, sph20-38 and sph30-38) and further inve ... | 2017 | 28600196 |
1,5-diaminopentane production from xylooligosaccharides using metabolically engineered corynebacterium glutamicum displaying beta-xylosidase on the cell surface. | xylooligosaccharide-assimilating corynebacterium glutamicum strains were constructed using metabolic engineering and cell surface display techniques. first, c. glutamicum was metabolically engineered to create lysine-producing strains. beta-xylosidase bsu17580 derived from bacillus subtilis was then expressed on the c. glutamicum cell surface using porh anchor protein, and enzymes involved in the xylose assimilation pathway were also expressed. metabolic engineering had no effect on the activity ... | 2017 | 28599919 |
molecular engineering of l-aspartate-α-decarboxylase for improved activity and catalytic stability. | β-alanine is an important precursor for the production of food additives, pharmaceuticals, and nitrogen-containing chemicals. compared with the conventional chemical routes for β-alanine production, the biocatalytic routes using l-aspartate-α-decarboxylase (adc) are more attractive when energy and environment are concerned. however, adc's poorly understood properties and its inherent mechanism-based inactivation significantly limited the application of this enzyme. in this study, three genes enc ... | 2017 | 28589224 |
development of a bacterial biosensor for rapid screening of yeast p-coumaric acid production. | transcription factor-based biosensors are used to identify producer strains, a critical bottleneck in cell factory engineering. here, we address two challenges with this methodology: transplantation of heterologous transcriptional regulators into new hosts to generate functional biosensors and biosensing of the extracellular product concentration that accurately reflects the effective cell factory production capacity. we describe the effects of different translation initiation rates on the dynam ... | 2017 | 28532147 |
comparative analysis of polyspecificity of the endogenous trna synthetase of different expression host towards photocrosslinking amino acids using an in silico approach. | photo-induced covalent crosslinking has emerged as the powerful strategy for analyzing and characterizing the protein-protein interaction and mapping protein 3d conformations. in the last decades, a number of photocrosslinking amino acids have been reported but only a few have been efficiently utilized for photocrosslinking purposes. recently, incorporation of diazirine containing photoactivatable analogs such as photo-methionine, photo-leucine, photo-isoleucine and photo-lysine into target prot ... | 2017 | 28641210 |
enhancing poly-γ-glutamic acid production in bacillus amyloliquefaciens by introducing the glutamate synthesis features from corynebacterium glutamicum. | poly-γ-glutamic acid (γ-pga) is a valuable polymer with glutamate as its sole precursor. enhancement of the intracellular glutamate synthesis is a very important strategy for the improvement of γ-pga production, especially for those glutamate-independent γ-pga producing strains. corynebacterium glutamicum has long been used for industrial glutamate production and it exhibits some unique features for glutamate synthesis; therefore introduction of these metabolic characters into the γ-pga producin ... | 2017 | 28532451 |
in vivo roles of fatty acid-biosynthetic enzymes in biosynthesis of biotin and α-lipoic acid in corynebacterium glutamicum. | for fatty acid biosynthesis, corynebacterium glutamicum uses two type i fatty acid synthases (fas-i), fasa and fasb, in addition to acetyl-coa carboxylase (acc) consisting of accbc, accd1, and acce. the in vivo roles of the enzymes in supplying precursors for biotin and α-lipoic acid remain unclear. here, we report genetic evidence demonstrating that the biosynthesis of these cofactors is linked to fatty acid biosynthesis through the fas-i pathway. for this study, we used wild-type c. glutamicum ... | 2017 | 28754705 |
engineering of corynebacterium glutamicum for consolidated conversion of hemicellulosic biomass into xylonic acid. | xylonic acid is a promising platform chemical with various applications in the fields of food, pharmaceuticals, and agriculture. however, in the current process, xylonic acid is mainly produced by the conversion of xylose, whose preparation requires substantial cost and time. here, we engineered corynebacterium glutamicum for the consolidated bioconversion of hemicellulosic biomass (xylan) into xylonic acid in a single cultivation. first, for the efficient conversion of xylose to xylonic acid, x ... | 2017 | 28799725 |
construction of recombinant pdu metabolosome shells for small molecule production in corynebacterium glutamicum. | bacterial microcompartments have significant potential in the area of industrial biotechnology for the production of small molecules, especially involving metabolic pathways with toxic or volatile intermediates. corynebacterium glutamicum is an established industrial workhorse for the production of amino acids and has been investigated for the production of a variety of further value-added products. herein, we describe components for the establishment of bacterial microcompartments as production ... | 2017 | 28826205 |
escherichia coli yjjpb genes encode a succinate transporter important for succinate production. | under anaerobic conditions, escherichia coli produces succinate from glucose via the reductive tricarboxylic acid cycle. to date, however, no genes encoding succinate exporters have been established in e. coli. therefore, we attempted to identify genes encoding succinate exporters by screening an e. coli mg1655 genome library. we identified the yjjpb genes as candidates encoding a succinate transporter, which enhanced succinate production in pantoea ananatis under aerobic conditions. a complemen ... | 2017 | 28673128 |
current status on metabolic engineering for the production of l-aspartate family amino acids and derivatives. | the l-aspartate amino acids (afaas) are constituted of l-aspartate, l-lysine, l-methionine, l-threonine and l-isoleucine. except for l-aspartate, afaas are essential amino acids that cannot be synthesized by humans and most farm animals, and thus possess wide applications in food, animal feed, pharmaceutical and cosmetics industries. to date, a number of amino acids, including afaas have been industrially produced by microbial fermentation. however, the overall metabolic and regulatory mechanism ... | 2017 | 28579173 |
production of amino acids - genetic and metabolic engineering approaches. | the biotechnological production of amino acids occurs at the million-ton scale and annually about 6milliontons of l-glutamate and l-lysine are produced by escherichia coli and corynebacterium glutamicum strains. l-glutamate and l-lysine production from starch hydrolysates and molasses is very efficient and access to alternative carbon sources and new products has been enabled by metabolic engineering. this review focusses on genetic and metabolic engineering of amino acid producing strains. in p ... | 2017 | 28552565 |
a new metabolic route for the fermentative production of 5-aminovalerate from glucose and alternative carbon sources. | here, a new metabolic pathway for the production of 5-aminovalerate (5ava) from l-lysine via cadaverine as intermediate was established and this three-step-pathway comprises l-lysine decarboxylase (ldcc), putrescine transaminase (pata) and γ-aminobutyraldehyde dehydrogenase (patd). since corynebacterium glutamicum is used for industrial l-lysine production, the pathway was established in this bacterium. upon expression of ldcc, pata and patd from escherichia coli in c. glutamicum wild type, prod ... | 2017 | 28522202 |
comparative analysis of the expression level of recombinant ginsenoside-transforming β-glucosidase in gras hosts and mass production of the ginsenoside rh2-mix. | the ginsenoside rh2, a pharmaceutically active component of ginseng, is known to have anticancer and antitumor effects. however, white ginseng and red ginseng have extremely low concentrations of rh2 or rh2-mix [20(s)-rh2, 20(r)-rh2, rk2, and rh3]. to enhance the production of food-grade ginsenoside rh2, an edible enzymatic bioconversion technique was developed adopting gras host strains. a β-glucosidase (bglpm), which has ginsenoside conversion ability, was expressed in three gras host strains ... | 2017 | 28423055 |
functional analysis of arabinofuranosidases and a xylanase of corynebacterium alkanolyticum for arabinoxylan utilization in corynebacterium glutamicum. | xylooligosaccharides (xoss) and arabinoxylooligosaccharides (axoss) are major oligosaccharides derived from arabinoxylan. in our previous report, corynebacterium glutamicum was engineered to utilize xoss by introducing corynebacterium alkanolyticum xyloside transporter and β-xylosidase. however, this strain was unable to consume axoss due to the absence of α-l-arabinofuranosidase activity. in this study, to confer axos utilization ability on c. glutamicum, two putative arabinofuranosidase genes ... | 2017 | 28409383 |
mutagenesis and redox partners analysis of the p450 fatty acid decarboxylase oletje. | the cytochrome p450 enzyme oletje from jeotgalicoccus sp. atcc 8456 is capable of converting free long-chain fatty acids into α-alkenes via one-step oxidative decarboxylation in presence of h2o2 as cofactor or using redox partner systems. this enzyme has attracted much attention due to its intriguing but unclear catalytic mechanism and potential application in biofuel production. here, we investigated the functionality of a select group of residues (arg245, cys365, his85, and ile170) in the acti ... | 2017 | 28276499 |
the antibacterial prodrug activator rv2466c is a mycothiol-dependent reductase in the oxidative stress response of mycobacterium tuberculosis. | the mycobacterium tuberculosis rv2466c gene encodes an oxidoreductase enzyme annotated as dsba. it has a cpwc active-site motif embedded within its thioredoxin fold domain and mediates the activation of the prodrug tp053, a thienopyrimidine derivative that kills both replicating and nonreplicating bacilli. however, its mode of action and actual enzymatic function in m. tuberculosis have remained enigmatic. in this study, we report that rv2466c is essential for bacterial survival under h2o2 stres ... | 2017 | 28620052 |
production of 5-aminovaleric acid in recombinant corynebacterium glutamicum strains from a miscanthus hydrolysate solution prepared by a newly developed miscanthus hydrolysis process. | this study examined nine expired industrial corynebacterium glutamicum strains with high lysine producing capability for enhanced production of 5-ava. c. glutamicum kctc 1857 exhibiting the highest lysine production was transformed with either original pseudomonas putida davba genes, encoding the 5-ava biosynthesis pathway, or c. glutamicum codon-optimized davba genes. c. glutamicum kctc 1857 expressing the original genes had superior cell viability and 5-ava production capability compared to th ... | 2017 | 28579174 |
bioprocess engineering to produce 9-(nonanoyloxy) nonanoic acid by a recombinant corynebacterium glutamicum-based biocatalyst. | here, corynebacterium glutamicum atcc13032 expressing baeyer-villiger monooxygenase from pseudomonas putida kt2440 was designed to produce 9-(nonanoyloxy) nonanoic acid from 10-ketostearic acid. diverse parameters including cultivation and reaction temperatures, type of detergent, and ph were found to improve biotransformation efficiency. the optimal temperature of cultivation for the production of 9-(nonanoyloxy) nonanoic acid from 10-ketostearic acid using whole cells of recombinant c. glutami ... | 2017 | 28567672 |
bio-based production of dimethyl itaconate from rice wine waste-derived itaconic acid. | dimethyl itaconate is an important raw material for copolymerization, but it is not synthesized from itaconic acid by organisms. moreover, corynebacterium glutamicum is used as an important industrial host for the production of organic acids, but it does not metabolize itaconic acid. therefore, the biosynthetic route towards dimethyl itaconate from itaconic acid is highly needed. in this study, we developed a biological procedure for dimethyl itaconate production from rice wine waste-derived ita ... | 2017 | 28846199 |
the three-component system esrisr regulates a cell envelope stress response in corynebacterium glutamicum. | when the cell envelope integrity is compromised, bacteria trigger signaling cascades resulting in the production of proteins that counteract these extracytoplasmic stresses. here, we show that the two-component system esrsr regulates a cell envelope stress response in the actinobacterium corynebacterium glutamicum. the sensor kinase esrs possesses an amino-terminal phage shock protein c (pspc) domain, a property that sets esrsr apart from all other two-component systems characterized so far. an ... | 2017 | 28922502 |
functional comparison of methionine sulphoxide reductase a and b in corynebacterium glutamicum. | methionine sulphoxide reductases (msr) are able to reduce methionine sulfoxide to methionine and protect bacteria against reactive oxygen species (ros). many organisms express both methionine sulphoxide reductase a (msra), specific for methionine-s-sulfoxide and methionine sulphoxide reductase b (msrb), active against methionine-r-sulfoxide. corynebacterium glutamicum expresses msra, the function of which has been well defined; however, the function of msrb has not been studied. whether msrb and ... | 2017 | 28904252 |
effect of lysine succinylation on the regulation of 2-oxoglutarate dehydrogenase inhibitor, odhi, involved in glutamate production in corynebacterium glutamicum. | in corynebacterium glutamicum, the activity of the 2-oxoglutarate dehydrogenase (odh) complex is negatively regulated by the unphosphorylated form of odhi protein, which is critical for l-glutamate overproduction. we examined the potential impact of protein acylation at lysine (k)-132 of odhi in c. glutamicum atcc13032. the k132e succinylation-mimic mutation reduced the ability of odhi to bind odha, the catalytic subunit of the odh complex, which reduced the inhibition of odh activity. in vitro ... | 2017 | 28899215 |
developing genome-reduced pseudomonas chlororaphis strains for the production of secondary metabolites. | the current chassis organisms or various types of cell factories have considerable advantages and disadvantages. therefore, it is necessary to develop various chassis for an efficient production of different bioproducts from renewable resources. in this context, synthetic biology offers unique potentialities to produce value-added products of interests. microbial genome reduction and modification are important strategies for constructing cellular chassis and cell factories. many genome-reduced s ... | 2017 | 28893188 |
amino acids production focusing on fermentation technologies - a review. | amino acids are attractive and promising biochemicals with market capacity requirements constantly increasing. their applicability ranges from animal feed additives, flavour enhancers and ingredients in cosmetic to specialty nutrients in pharmaceutical and medical fields. this review gives an overview of the processes applied for amino acids production and points out the main advantages and disadvantages of each. due to the advances made in the genetic engineering techniques, the biotechnologica ... | 2017 | 28888551 |
synthetic biology for manufacturing chemicals: constraints drive the use of non-conventional microbial platforms. | genetically modified microbes have had much industrial success producing protein-based products (such as antibodies and enzymes). however, engineering microbial workhorses for biomanufacturing of commodity compounds remains challenging. first, microbes cannot afford burdens with both overexpression of multiple enzymes and metabolite drainage for product synthesis. second, synthetic circuits and introduced heterologous pathways are not yet as "robust and reliable" as native pathways due to hosts' ... | 2017 | 28884354 |
[biocatalytic access to β-alanine by a two-enzyme cascade synthesis]. | enzymatic synthesis is an important way to produce β-alanine, but the biological method is expensive generally because of the high price of substrate. in this paper, a two-step enzymatic cascade system was developed, combining l-aspartase from escherichia coli dh5α and l-aspartate α-decarboxylase from corynebacterium glutamicum. this system catalyzes fumarate and ammonia to β-alanine. the optimal ratio of aspa and pand was 1:80 (w/w), and the concentration of aspa was 10 μg/ml, at 37 ℃ and ph 7. ... | 2017 | 28876041 |
identification and functional characterization of small alarmone synthetases in corynebacterium glutamicum. | the hyperphosphorylated guanosine derivatives ppgpp and pppgpp represent global regulators of the bacterial stress response, as they act as central elements of the stringent response system. although it was assumed that both, (p)ppgpp synthesis and hydrolysis, are catalyzed by one bifunctional rsh-protein in the actinobacterial model organism corynebacterium glutamicum atcc 13032, two putative short alarmone synthetases (sass) were identified by bioinformatic analyses. the predicted sequences of ... | 2017 | 28871248 |
enhanced biosynthesis of hyaluronic acid using engineered corynebacterium glutamicum via metabolic pathway regulation. | hyaluronic acid (ha) is a polysaccharide used in many industries such as medicine, surgery, cosmetics and food. to avoid potential pathogenicity caused by its native producer, streptococcus, efforts have been made to create a recombinant host for ha production. in this work, a gras (generally recognized as safe) strain, corynebacterium glutamicum, was engineered for enhanced biosynthesis of ha via metabolic pathway regulation. five enzymes (hasa-hase) involved in the ha biosynthetic pathway were ... | 2017 | 28869338 |
cgii cleaves dna using a mechanism distinct from other atp-dependent restriction endonucleases. | the restriction endonuclease cgli from corynebacterium glutamicum recognizes an asymmetric 5'-gccgc-3' site and cleaves the dna 7 and 6/7 nucleotides downstream on the top and bottom dna strands, respectively, in an ntp-hydrolysis dependent reaction. cgli is composed of two different proteins: an endonuclease (r.cgli) and a dead-family helicase-like atpase (h.cgli). these subunits form a heterotetrameric complex with r2h2 stoichiometry. however, the r2h2·cgli complex has only one nuclease active ... | 2017 | 28854738 |
structure, function, and regulation of enzymes involved in amino acid metabolism of bacteria and archaea. | amino acids are essential components in all organisms because they are building blocks of proteins. they are also produced industrially and used for various purposes. for example, l-glutamate is used as the component of "umami" taste and lysine has been used as livestock feed. recently, many kinds of amino acids have attracted attention as biological regulators and are used for a healthy life. thus, to clarify the mechanism of how amino acids are biosynthesized and how they work as biological re ... | 2017 | 28840778 |
ph fluctuations imperil the robustness of c. glutamicum to short term oxygen limitation. | the presence of complex gradients for, e.g., nutrients, oxygen or ph in industrial scale fed batch processes are a major challenge for process performance. to consider such impact of scale-up during laboratory scale process development, scale-down bioreactor simulation, i.e. mimicking inhomogeneous conditions, became the method of choice. however, most scale-down studies simulate combined inhomogeneities of more than one parameter, so that the impact of the individual parameters remains unclear. ... | 2017 | 28837821 |
chemical shift assignments of polyketide cyclase_like protein cgl2373 from corynebacterium glutamicum. | protein cgl2373 from corynebacterium glutamicum, which is 155 amino acids long and 17.7 kda, is a member of the polyketide_cyc2 family. as a potential polyketide cyclase, it may play an important role in the biosynthesis of aromatic polyketides that are the source of many bioactive molecules. here we report the complete (1)h, (13)c and (15)n chemical shift assignments of cgl2373, which lays a foundation for further structural and functional research. | 2017 | 28825188 |
polymerization dynamics of the prophage-encoded actin-like protein alpc is influenced by the dna-binding adapter alpa. | the corynebacterium glutamicum atcc 13032 prophage cgp3 encodes an actin-like protein, alpc that was shown to be involved in viral dna transport and efficient viral dna replication. alpc binds to an adapter, alpa that in turn binds to specific dna sequences, termed alps sites. thus, the alpac system is similar to the known plasmid segregation system parmrs. so far it is unclear how the alpacs system mediates dna transport and, whether alpa and alpc functionally interact. we show here that alpa m ... | 2017 | 28824563 |
corynebacterium glutamicum chassis c1*: building and testing a novel platform host for synthetic biology and industrial biotechnology. | targeted top-down strategies for genome reduction are considered to have a high potential for providing robust basic strains for synthetic biology and industrial biotechnology. recently, we created a library of 26 genome-reduced strains of corynebacterium glutamicum carrying broad deletions in single gene clusters and showing wild-type-like biological fitness. here, we proceeded with combinatorial deletions of these irrelevant gene clusters in two parallel orders, and the resulting library of 28 ... | 2017 | 28803482 |
recombineering using recet in corynebacterium glutamicum atcc14067 via a self-excisable cassette. | gene manipulation is essential for metabolic engineering and synthetic biology, but the current general gene manipulation methods are not applicable to the non-model strain corynebacterium glutamicum (c. glutamicum) atcc14067, which is used for amino acid production. here, we report an effective and sequential deletion method for c. glutamicum atcc14067 using the exonuclease-recombinase pair rece + rect (recet) for recombineering via a designed self-excisable linear double-strand dna (dsdna) cas ... | 2017 | 28801604 |
physiological roles of sigma factor sigd in corynebacterium glutamicum. | sigma factors are one of the components of rna polymerase holoenzymes, and an essential factor of transcription initiation in bacteria. corynebacterium glutamicum possesses seven genes coding for sigma factors, most of which have been studied to some detail; however, the role of sigd in transcriptional regulation in c. glutamicum has been mostly unknown. | 2017 | 28701150 |
development of a single-cell glxr-based camp biosensor for corynebacterium glutamicum. | cyclic adenosine monophosphate (camp) plays a regulatory role as second messenger in many species. in the industrial model organism corynebacterium glutamicum, camp acts as effector of the global transcriptional regulator glxr, a homolog of enterobacterial crp. the camp-glxr complex activates or represses the expression of about 200 target genes. cyab, a membrane-bound class iii adenylate cyclase, synthesizes camp from atp, but another yet unknown camp-forming enzyme is likely present in c. glut ... | 2017 | 28698098 |
a new genome-scale metabolic model of corynebacterium glutamicum and its application. | corynebacterium glutamicum is an important platform organism for industrial biotechnology to produce amino acids, organic acids, bioplastic monomers, and biofuels. the metabolic flexibility, broad substrate spectrum, and fermentative robustness of c. glutamicum make this organism an ideal cell factory to manufacture desired products. with increases in gene function, transport system, and metabolic profile information under certain conditions, developing a comprehensive genome-scale metabolic mod ... | 2017 | 28680478 |
structural insights into substrate specificity of cystathionine γ-synthase from corynebacterium glutamicum. | cystathionine γ-synthase (metb) condenses o-acetyl-l-homoserine (oahs) or o-succinyl-l-homoserine (oshs) with cysteine to produce cystathionine. to investigate the molecular mechanisms and substrate specificity of metb from corynebacterium glutamicum (cgmetb), we determined its crystal structure at 1.5 å resolution. the pyridoxal phosphate cofactor is covalently bound to lys204 via a schiff base linkage in the deep cavity. superposition with the structure of metb from nicotiana tabacum in comple ... | 2017 | 28675039 |
assignment of sigma factors of rna polymerase to promoters in corynebacterium glutamicum. | corynebacterium glutamicum is an important industrial producer of various amino acids and other metabolites. the c. glutamicum genome encodes seven sigma subunits (factors) of rna polymerase: the primary sigma factor siga (σ(a)), the primary-like σ(b) and five alternative sigma factors (σ(c), σ(d), σ(e), σ(h) and σ(m)). we have developed in vitro and in vivo methods to assign particular sigma factors to individual promoters of different classes. in vitro transcription assays and measurements of ... | 2017 | 28651382 |
crispr/cas9-coupled recombineering for metabolic engineering of corynebacterium glutamicum. | genome engineering of corynebacterium glutamicum, an important industrial microorganism for amino acids production, currently relies on random mutagenesis and inefficient double crossover events. here we report a rapid genome engineering strategy to scarlessly knock out one or more genes in c. glutamicum in sequential and iterative manner. recombinase rect is used to incorporate synthetic single-stranded oligodeoxyribonucleotides into the genome and crispr/cas9 to counter-select negative mutants ... | 2017 | 28649005 |
the linkage between nutrient supply, intracellular enzyme abundances and bacterial growth: new evidences from the central carbon metabolism of corynebacterium glutamicum. | corynebacterium glutamicum serves as important production host for small molecular compounds that are derived from precursor molecules of the central carbon metabolism. it is therefore a well-studied model organism of industrial biotechnology. however, a deeper understanding of the regulatory principles underlying the synthesis of central metabolic enzymes under different environmental conditions as well as its impact on cell growth is still missing. we studied enzyme abundances in c. glutamicum ... | 2017 | 28647528 |
biotransformation of ferulic acid to protocatechuic acid by corynebacterium glutamicum atcc 21420 engineered to express vanillate o-demethylase. | ferulic acid (4-hydroxy-3-methoxycinnamic acid, fa) is a lignin-derived phenolic compound abundant in plant biomass. the utilization of fa and its conversion to valuable compounds is desired. protocatechuic acid (3,4-dihydroxybenzoic acid, pca) is a precursor of polymers and plastics and a constituent of food. a microbial conversion system to produce pca from fa was developed in this study using a pca-producing strain of corynebacterium glutamicum f (atcc 21420). c. glutamicum strain f grown at ... | 2017 | 28641405 |
selective oxidation of aliphatic c-h bonds in alkylphenols by a chemomimetic biocatalytic system. | selective oxidation of aliphatic c-h bonds in alkylphenols serves significant roles not only in generation of functionalized intermediates that can be used to synthesize diverse downstream chemical products, but also in biological degradation of these environmentally hazardous compounds. chemo-, regio-, and stereoselectivity; controllability; and environmental impact represent the major challenges for chemical oxidation of alkylphenols. here, we report the development of a unique chemomimetic bi ... | 2017 | 28607077 |
enhancement of anaerobic lysine production in corynebacterium glutamicum electrofermentations. | it has been suggested that application of electric potential can affect lysine producing fermentations, although experimental evidence is lacking. to study this hypothesis we used the lysine producer corynebacterium glutamicum zw04, and we exposed it to 12 different conditions regarding anaerobic gas environment, applied electrode potential (cathodic, open circuit, anodic), redox mediator and nitrate presence. the gas environment was found to play a major role, with co2 leading to double the lys ... | 2017 | 28599233 |
novel chromosome organization pattern in actinomycetales-overlapping replication cycles combined with diploidy. | bacteria regulate chromosome replication and segregation tightly with cell division to ensure faithful segregation of dna to daughter generations. the underlying mechanisms have been addressed in several model species. it became apparent that bacteria have evolved quite different strategies to regulate dna segregation and chromosomal organization. we have investigated here how the actinobacterium corynebacterium glutamicum organizes chromosome segregation and dna replication. unexpectedly, we fo ... | 2017 | 28588128 |
metabolic design of corynebacterium glutamicum for production of l-cysteine with consideration of sulfur-supplemented animal feed. | l-cysteine is a valuable sulfur-containing amino acid widely used as a nutrition supplement in industrial food production, agriculture, and animal feed. however, this amino acid is mostly produced by acid hydrolysis and extraction from human or animal hairs. in this study, we constructed recombinant corynebacterium glutamicum strains that overexpress combinatorial genes for l-cysteine production. the aims of this work were to investigate the effect of the combined overexpression of serine acetyl ... | 2017 | 28560868 |
miniaturized and automated adaptive laboratory evolution: evolving corynebacterium glutamicum towards an improved d-xylose utilization. | adaptive laboratory evolution (ale) is increasingly being used as a technique for untargeted strain optimization. this work aimed at developing an automated and miniaturized ale approach based on repetitive batch cultivations in microtiter plates. the new method is applied to the recently published strain corynebacterium glutamicum pekex3-xylxabcdcc, which is capable of utilizing d-xylose via the weimberg (wmb) pathway. as a result, the significantly improved strain wmb2evo was obtained, showing ... | 2017 | 28552568 |
enhancement of 5-aminolevulinic acid production by metabolic engineering of the glycine biosynthesis pathway in corynebacterium glutamicum. | to construct a strain of corynebacterium glutamicum capable of efficiently producing 5-aminolevulinic acid (5-ala) via the c4 pathway by modification of serine and glycine pathway using glucose as sole carbon source. | 2017 | 28536938 |
overexpression of ppc or deletion of mdh for improving production of γ-aminobutyric acid in recombinant corynebacterium glutamicum. | l-glutamate decarboxylase (gad) transforms l-glutamate into γ-aminobutyric acid (gaba). corynebacterium glutamicum that expresses exogenous gad gene(s) can synthesize gaba from its own produced l-glutamate. to enhance gaba production in recombinant c. glutamicum strain sh, metabolic engineering strategies were used to improve the supply of the gaba precursor, l-glutamate. five new strains were constructed here. first, the ppc gene was coexpressed with two gad genes (gadb1 and gadb2). then, the m ... | 2017 | 28534111 |
y418 in 410s loop is required for high transglucosylation activity and large-ring cyclodextrin production of amylomaltase from corynebacterium glutamicum. | amylomaltase catalyzes α-1,4 glucosyl transfer reaction to yield linear or cyclic oligosaccharide products. the aim of this work is to investigate functional roles of 410s loop unique to amylomaltase from corynebacterium glutamicum (cgam). site-directed mutagenesis of y418, the residue at the loop tip, was performed. y418a/s/d/r/w/f - cgams were characterized and compared to the wild-type (wt). a significant decrease in starch transglucosylation, disproportionation and cyclization activities was ... | 2017 | 28522291 |
crystal structure of the 2-iminoglutarate-bound complex of glutamate dehydrogenase from corynebacterium glutamicum. | the nadp(+) -dependent glutamate dehydrogenase from corynebacterium glutamicum (cggdh) is considered to be one of the key enzymes in the industrial fermentation of glutamate due to its high glutamate-producing activity. we determined the crystal structure of cggdh complexed with nadp(+) and 2-iminoglutarate. among six subunits of hexameric cggdh-binding nadp(+) , only four subunits bind 2-iminoglutarate in a closed form, while the other two are in an open form. in the closed form, 2-iminoglutara ... | 2017 | 28486765 |
isoprenoid pyrophosphate-dependent transcriptional regulation of carotenogenesis in corynebacterium glutamicum. | corynebacterium glutamicum is a natural producer of the c50 carotenoid decaprenoxanthin. the crtecg0722crtbiyeb operon comprises most of its genes for terpenoid biosynthesis. the marr-type regulator encoded upstream and in divergent orientation of the carotenoid biosynthesis operon has not yet been characterized. this regulator, named crtr in this study, is encoded in many actinobacterial genomes co-occurring with terpenoid biosynthesis genes. crtr was shown to repress the crt operon of c. gluta ... | 2017 | 28484430 |
improved fermentative production of the compatible solute ectoine by corynebacterium glutamicum from glucose and alternative carbon sources. | the cyclic amino acid ectoine is a compatible solute serving as a protective substance against osmotic stress. ectoine finds various applications due to its moisturizing effect. to avoid the disadvantages of the prevailing so-called "bacterial milking ectoine production process" caused by the high salt concentration, low salt fermentation strategies are sought after. as l-lysine and ectoine biosynthesis share l-aspartate-semialdehyde as common precursor, l-lysine producing strains can be convert ... | 2017 | 28478080 |
complete nucleotide sequence and annotation of the temperate corynephage ϕ16 genome. | the complete genome of ϕ16, a temperate corynephage from corynebacterium glutamicum atcc 21792, was sequenced and annotated (genbank: ky250482). the electron microscopy study of ϕ16 virion confirmed that it belongs to the family siphoviridae. the ϕ16 genome consists of a linear double-stranded dna molecule of 58,200 bp (g+c = 52.2%) with protruding cohesive 3'-ends of 14 nt. four major structural proteins were separated by sds-page and identified by peptide mass fingerprinting technique. using b ... | 2017 | 28455670 |
the arsenic detoxification system in corynebacteria: basis and application for bioremediation and redox control. | arsenic (as) is widespread in the environment and highly toxic. it has been released by volcanic and anthropogenic activities and causes serious health problems worldwide. to survive arsenic-rich environments, soil and saprophytic microorganisms have developed molecular detoxification mechanisms to survive arsenic-rich environments, mainly by the enzymatic conversion of inorganic arsenate (as(v)) to arsenite (as(iii)) by arsenate reductases, which is then extruded by arsenite permeases. one of t ... | 2017 | 28438267 |
genome-wide determination of transcription start sites reveals new insights into promoter structures in the actinomycete corynebacterium glutamicum. | the genome-wide identification of transcription start sites, enabled by high-throughput sequencing of a cdna library enriched for native 5' transcript ends, is ideally suited for the analysis of promoters. here, the transcriptome of corynebacterium glutamicum, a non-pathogenic soil bacterium from the actinomycetes branch that is used in industry for the production of amino acids, was analysed by transcriptome sequencing of the 5'-ends of native transcripts. total rna samples were harvested from ... | 2017 | 28412515 |
dynamic flux balance analysis with nonlinear objective function. | dynamic flux balance analysis (dfba) extends flux balance analysis and enables the combined simulation of both intracellular and extracellular environments of microbial cultivation processes. a dfba model contains two coupled parts, a dynamic part at the upper level (extracellular environment) and an optimization part at the lower level (intracellular environment). both parts are coupled through substrate uptake and product secretion rates. this work proposes a karush-kuhn-tucker condition based ... | 2017 | 28401266 |
analysis of strain-specific genes in glutamic acid-producing corynebacterium glutamicum ssp. lactofermentum aj 1511. | strains of the bacterium, corynebacterium glutamicum, are widely used for the industrial production of l-glutamic acid and various other substances. c. glutamicum ssp. lactofermentum aj 1511, formerly classified as brevibacterium lactofermentum, and the closely related c. glutamicum atcc 13032 have been used as industrial strains for more than 50 years. we determined the whole genome sequence of c. glutamicum aj 1511 and performed genome-wide comparative analysis with c. glutamicum atcc 13032 to ... | 2017 | 28392541 |
identification of specific posttranslational o-mycoloylations mediating protein targeting to the mycomembrane. | the outer membranes (oms) of members of the corynebacteriales bacterial order, also called mycomembranes, harbor mycolic acids and unusual outer membrane proteins (omps), including those with α-helical structure. the signals that allow precursors of such proteins to be targeted to the mycomembrane remain uncharacterized. we report here the molecular features responsible for omp targeting to the mycomembrane of corynebacterium glutamicum, a nonpathogenic member of the corynebacteriales order. to ... | 2017 | 28373551 |
transcriptome analysis of corynebacterium glutamicum in the process of recombinant protein expression in bioreactors. | corynebacterium glutamicum (c. glutamicum) is a favorable host cell for the production of recombinant proteins, such as important enzymes and pharmaceutical proteins, due to its excellent potential advantages. herein, we sought to systematically explore the influence of recombinant protein expression on the transcription and metabolism of c. glutamicum. two c. glutamicum strains, the wild-type strain and an engineered strain expressing enhanced green fluorescent protein (egfp), were cultured in ... | 2017 | 28369109 |
a novel genetic tool for metabolic optimization of corynebacterium glutamicum: efficient and repetitive chromosomal integration of synthetic promoter-driven expression libraries. | fine-tuning the expression level of multiple genes is usually pivotal for metabolic optimization. we have developed a tool for this purpose for the important industrial workhorse corynebacterium glutamicum that allows for the introduction of synthetic promoter-driven expression libraries of arbitrary genes. we first devised a method for introducing genetic elements into the chromosome repeatedly, relying on site-specific recombinases and the vector pjs31 serving as the carrier. the pjs31 vector ... | 2017 | 28361238 |
a newly determined member of the meso-diaminopimelate dehydrogenase family with a broad substrate spectrum. | meso-diaminopimelate dehydrogenase (meso-dapdh) from symbiobacterium thermophilum (stdapdh) is the first member of the meso-dapdh family known to catalyze the asymmetric reductive amination of 2-keto acids to produce d-amino acids. it is important to understand the catalytic mechanisms of stdapdh and other enzymes in this family. in this study, based on an evolutionary analysis and examination of catalytic activity, the meso-dapdh enzymes can be divided into two types. type i showed highly prefe ... | 2017 | 28341677 |
proteomics of facs-sorted heterogeneous corynebacterium glutamicum populations. | the metabolic status of individual cells in microbial cultures can differ, being relevant for biotechnology, environmental and medical microbiology. however, it is hardly understood in molecular detail due to limitations of current analytical tools. here, we demonstrate that facs in combination with proteomics can be used to sort and analyze cell populations based on their metabolic state. a previously established gfp reporter system was used to detect and sort single corynebacterium glutamicum ... | 2017 | 28323243 |
similarities in the structure of the transcriptional repressor amtr in two different space groups suggest a model for the interaction with glnk. | amtr belongs to the tetr family of transcription regulators and is a global nitrogen regulator that is induced under nitrogen-starvation conditions in corynebacterium glutamicum. amtr regulates the expression of transporters and enzymes for the assimilation of ammonium and alternative nitrogen sources, for example urea, amino acids etc. the recognition of operator dna by homodimeric amtr is not regulated by small-molecule effectors as in other tetr-family members but by a trimeric adenylylated p ... | 2017 | 28291750 |
characterization of lysine acetylation of a phosphoenolpyruvate carboxylase involved in glutamate overproduction in corynebacterium glutamicum. | protein nε-acylation is emerging as a ubiquitous post-translational modification. in corynebacterium glutamicum, which is utilized for industrial production of l-glutamate, the levels of protein acetylation and succinylation change drastically under the conditions that induce glutamate overproduction. here, the acylation of phosphoenolpyruvate carboxylase (pepc), an anaplerotic enzyme that supplies oxaloacetate for glutamate overproduction was characterized. it was shown that acetylation of pepc ... | 2017 | 28256782 |
complete genome sequencing of newly isolated thermotolerant corynebacterium glutamicum n24 provides a new insights into its thermotolerant phenotype. | to understand the genetic background of thermotolerance, we determined the complete genome sequence of a thermotolerant corynebacterium glutamicum n24 strain isolated from soil. the whole genome based phylogenetic analysis between n24 and other related species revealed that n24 diverged from other c. glutamicum strains at earlier stages. comparisons of thermotolerance between n24 and its related species showed that n24 and corynebacterium efficiens ys-314 have a higher thermotolerance than coryn ... | 2017 | 28249784 |
beyond amino acids: use of the corynebacterium glutamicum cell factory for the secretion of heterologous proteins. | the gram-positive soil bacterium corynebacterium glutamicum has a long tradition in industry as a potent cell factory for the production of various amino acids. besides this, in the last few years it became increasingly clear that this microorganism can also efficiently be used as a host organism for the expression and secretion of biotechnologically or pharmaceutically relevant heterologous proteins. in this review, first a short overview is given on the two main protein export pathways (sec an ... | 2017 | 28238807 |
improvement of succinate production by release of end-product inhibition in corynebacterium glutamicum. | succinate is a renewable-based platform chemical that may be used to produce a wide range of chemicals including 1,4-butanediol, tetrahydrofurane, and γ-butyrolactone. however, industrial fermentation of organic acids is often subject to end-product inhibition, which significantly retards cell growth and limits metabolic activities and final productivity. in this study, we report the development of metabolically engineered corynebacterium glutamicum for high production of succinate by release of ... | 2017 | 28232033 |
click-chemistry approach to study mycoloylated proteins: evidence for porb and porc porins mycoloylation in corynebacterium glutamicum. | protein mycoloylation is a recently identified, new form of protein acylation. this post-translational modification consists in the covalent attachment of mycolic acids residues to serine. mycolic acids are long chain, α-branched, β-hydroxylated fatty acids that are exclusively found in the cell envelope of corynebacteriales, a bacterial order that includes important genera such as mycobacterium, nocardia or corynebacterium. so far, only 3 mycoloylated proteins have been identified: pora, porh a ... | 2017 | 28199365 |
comparative analysis of corynebacterium glutamicum genomes: a new perspective for the industrial production of amino acids. | corynebacterium glutamicum is a non-pathogenic bacterium widely used in industrial amino acid production and metabolic engineering research. although the genome sequences of some c. glutamicum strains are available, comprehensive comparative genome analyses of these species have not been done. six wild type c. glutamicum strains were sequenced using next-generation sequencing technology in our study. together with 20 previously reported strains, we present a comprehensive comparative analysis of ... | 2017 | 28198668 |
cofactor recycling for co-production of 1,3-propanediol and glutamate by metabolically engineered corynebacterium glutamicum. | production of 1,3-propanediol (1,3-pdo) from glycerol is a promising route toward glycerol biorefinery. however, the yield of 1,3-pdo is limited due to the requirement of nadh regeneration via glycerol oxidation process, which generates large amounts of undesired byproducts. glutamate fermentation by corynebacterium glutamicum is an important oxidation process generating excess nadh. in this study, we proposed a novel strategy to couple the process of 1,3-pdo synthesis with glutamate production ... | 2017 | 28176878 |
structural basis for redox sensitivity in corynebacterium glutamicum diaminopimelate epimerase: an enzyme involved in l-lysine biosynthesis. | diaminopimelate epimerase (dapf) is one of the crucial enzymes involved in l-lysine biosynthesis, where it converts l,l-diaminopimelate (l,l-dap) into d,l-dap. dapf is also considered as an attractive target for the development of antibacterial drugs. here, we report the crystal structure of dapf from corynebacterium glutamicum (cgdapf). structures of cgdapf obtained under both oxidized and reduced conditions reveal that the function of cgdapf is regulated by redox-switch modulation via reversib ... | 2017 | 28176858 |
fermentative production of l-pipecolic acid from glucose and alternative carbon sources. | corynebacterium glutamicum is used for the million-ton scale production of amino acids and has recently been engineered for production of the cyclic non-proteinogenic amino acid l-pipecolic acid (l-pa). in this synthetic pathway l-lysine was converted to l-pa by oxidative deamination, dehydration and reduction by l-lysine 6-dehydrogenase (deaminating) from silicibacter pomeroyi and pyrroline 5-carboxylate reductase from c. glutamicum. however, production of l-pa occurred as by-product of l-lysin ... | 2017 | 28169491 |
l-lysine production by bacillus methanolicus: genome-based mutational analysis and l-lysine secretion engineering. | bacillus methanolicus is a methylotrophic bacterium with an increasing interest in academic research and for biotechnological applications. this bacterium was previously applied for methanol-based production of l-glutamate, l-lysine and the five-carbon diamine cadaverine by wild type, classical mutant and recombinant strains. the genomes of two different l-lysine secreting b. methanolicus classical mutant strains, noa2#13a52-8a66 and m168-20, were sequenced. we focused on mutational mapping in g ... | 2017 | 28163092 |
modular pathway engineering of corynebacterium glutamicum to improve xylose utilization and succinate production. | xylose-negative corynebacterium glutamicum has been engineered to utilize xylose as the sole carbon source via either the xylose isomerase (xi) pathway or the weimberg pathway. heterologous expression of xylose isomerase and overexpression of a gene encoding for xylulose kinase enabled efficient xylose utilization. in this study, we show that two functionally-redundant transcriptional regulators (gntr1 and gntr2) present on xylose repress the pentose phosphate pathway genes. for efficient xylose ... | 2017 | 28153765 |
comprehensive and accurate tracking of carbon origin of lc-tandem mass spectrometry collisional fragments for (13)c-mfa. | in recent years the benefit of measuring positionally resolved (13)c-labeling enrichment from tandem mass spectrometry (ms/ms) collisional fragments for improved precision of (13)c-metabolic flux analysis ((13)c-mfa) has become evident. however, the usage of positional labeling information for (13)c-mfa faces two challenges: (1) the mass spectrometric acquisition of a large number of potentially interfering mass transitions may hamper accuracy and sensitivity. (2) the positional identity of carb ... | 2017 | 28116490 |
rational design of substrate binding pockets in polyphosphate kinase for use in cost-effective atp-dependent cascade reactions. | adenosine-5'-triphosphate (atp) is the energy equivalent of the living system. polyphosphate (polyp) is the ancient energy storage equivalent of organisms. polyphosphate kinases (ppks) catalyze the polyp formation or atp formation, to store energy or to regenerate atp, respectively. however, most ppks are active only in the presence of long polyps, which are more difficult and more expensive to generate than the short polyps. we investigated the ppk preference towards polyps by site-directed mut ... | 2017 | 28417169 |
crispr-cpf1 assisted genome editing of corynebacterium glutamicum. | corynebacterium glutamicum is an important industrial metabolite producer that is difficult to genetically engineer. although the streptococcus pyogenes (sp) crispr-cas9 system has been adapted for genome editing of multiple bacteria, it cannot be introduced into c. glutamicum. here we report a francisella novicida (fn) crispr-cpf1-based genome-editing method for c. glutamicum. crispr-cpf1, combined with single-stranded dna (ssdna) recombineering, precisely introduces small changes into the bact ... | 2017 | 28469274 |
a novel synthetic pathway enables microbial production of polyphenols independent from the endogenous aromatic amino acid metabolism. | numerous plant polyphenols have potential applications as pharmaceuticals or nutraceuticals. stilbenes and flavonoids as most abundant polyphenols are synthesized from phenylpropanoids, which are exclusively derived from aromatic amino acids in nature. several microorganisms were engineered for the synthesis of biotechnologically interesting plant polyphenols; however, low activity of heterologous ammonia lyases, linking endogenous microbial aromatic amino acid biosynthesis to phenylpropanoid sy ... | 2017 | 27936616 |
glutamate fermentation-2: mechanism of l-glutamate overproduction in corynebacterium glutamicum. | the nonpathogenic coryneform bacterium, corynebacterium glutamicum, was isolated as an l-glutamate-overproducing microorganism by japanese researchers and is currently utilized in various amino acid fermentation processes. l-glutamate production by c. glutamicum is induced by limitation of biotin and addition of fatty acid ester surfactants and β-lactam antibiotics. these treatments affect the cell surface structures of c. glutamicum. after the discovery of c. glutamicum, many researchers have i ... | 2017 | 27913829 |
discovery and history of amino acid fermentation. | there has been a strong demand in japan and east asia for l-glutamic acid as a seasoning since monosodium glutamate was found to present umami taste in 1907. the discovery of glutamate fermentation by corynebacterium glutamicum in 1956 enabled abundant and low-cost production of the amino acid, creating a large market. the discovery also prompted researchers to develop fermentative production processes for other l-amino acids, such as lysine. currently, the amino acid fermentation industry is so ... | 2017 | 27909736 |
the whcd gene of corynebacterium glutamicum plays roles in cell division and envelope formation. | in this study, we analysed the whcd gene from corynebacteriumglutamicum, which encodes a homologue of whib, a streptomycescoelicolor gene required for the sporulation of aerial hyphae. deletion of the gene (δwhcd) severely affected cell growth in c. glutamicum. the δwhcd strain exhibited a large filamentous, branched and bud-shaped morphology with multiple septa. the transcription levels of the cell division genes involved in z-ring assembly and septal peptidoglycan synthesis, including ftsz, se ... | 2017 | 27902442 |
expansion of the substrate range of the gentisate 1,2-dioxygenase from corynebacterium glutamicum for the conversion of monohydroxylated benzoates. | the gentisate 1,2-dioxygenases (gdos) from corynebacterium glutamicum and various other organisms oxidatively cleave the aromatic nucleus of gentisate (2,5-dihydroxybenzoate), but are not able to convert salicylate (2-hydroxybenzoate). in contrast, the α-proteobacterium pseudaminobacter salicylatoxidans synthesises an enzyme ('salicylate dioxygenase', sdo) which cleaves gentisate, but also (substituted) salicylate(s). sequence comparisons showed that the sdo belongs to a group of gdos mainly ori ... | 2017 | 27887027 |