Publications

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[demonstration of easily exchangeable acetaldehyde during ethanol oxidation by acetobacter rancens particles]. 19704985242
[presence of polyphosphateglucokinase in bacteria]. 19684989012
[basic proteins in the process of leukocyte maturation]. 19715003745
[the synthesis and beta-lactamase inhibition activity of p-(3-amido-4-substituted phenyl-2-azetidinonyl-1)-phenylacetic acids and p-(3-amido-4-substituted phenyl-2-azetidinonyl-1)-acetophenones]. 19883138889
effect of amino acids on the growth of acetobacter suboxydans. 19725026267
the serum polyol pattern and the urinary polyol excretion in diabetic and in uremic patients. 19725031782
photographic applications in birefringence investigations. 19725043862
preparation and characterization of monoclonal antibodies to cephalexin-synthesizing enzyme from acetobacter turbidans.eleven monoclonal antibodies against the cephalexin-synthesizing enzyme have been constructed and primarily characterized. these antibodies are all igg1 type, with medium affinity, and with no enzyme-inhibition effect. they will be utilized as immunoadsorbents to purify their corresponding antigen, the enzyme, in one step.19883169806
factors affecting hexose phosphorylation in acetobacter xylinum.fructose was oxidized and converted to cellulose by cells of acetobacter xylinum grown on fructose or succinate, but not by cells grown on glucose. in resting fructose-grown cells, glucose strongly suppressed fructose utilization. extracts obtained from fructose- or succinate-grown cells catalyzed the adenosine triphosphate (atp)-dependent formation of the 6-phosphate esters of glucose and fructose, whereas glucose-grown cell extracts phosphorylated glucose but not fructose. fructokinase and glu ...19725053462
naturally occurring monobactams. 19863521210
[numerical taxonomy of pseudomonads of the diminuta group].the taxonomy of the "diminuta" group is discussed. the method of numerical taxonomy was used to characterize 135 strains of 10 species belonging to pseudomonas, gluconobacter and acetobacter in terms of sixty phenotypical features. the similarity coefficients of the strains were calculated with computers. according to the data of numerical analysis, the species p. diminuta and p. vesiculare represent a single phenon different from pseudomonas, gluconobacter and acetobacter species.19863702780
cellulose microfibril assembly and orientation: recent developments.a brief history of the literature dealing with cellulose microfibril assembly is presented, and a current summary of cellulose microfibril synthesizing complexes among eukaryotic cells is given. terminal complexes not described before include the following: linear terminal complexes (tcs) with three rows in eremosphaera, microdictyon and chaetomorpha; globular terminal complexes in ophioglossum, psilotum, equisetum and gingko. cellulose microfibril assembly in acetobacter xylinum is described ve ...19853867669
acetylene as a competitive inhibitor of n-2 fixation. 19675231601
prokaryotic triterpenoids. 1. 3 beta-methylhopanoids from acetobacter species and methylococcus capsulatus.3 beta-methylbacteriohopanepolyol derivatives were isolated from three bacteria, acetobacter pasteurianus ssp. pasteurianus, methylococcus capsulatus and nostoc muscorum, and identified by spectroscopic methods and direct comparison with 3 beta-methyldiplopterol and 3 beta-methylhopan-29-ol synthesized from 22-hydroxyhopan-3-one. the 3 beta-methylhopanoid content of a. pasteurianus ssp. pasteurianus could be dramatically increased (up to 60% of the total hopanoid content) by addition of l-methio ...19853926494
prokaryotic triterpenoids. 3. the biosynthesis of 2 beta-methylhopanoids and 3 beta-methylhopanoids of methylobacterium organophilum and acetobacter pasteurianus ssp. pasteurianus.the incorporation of l-[methyl-3h,14c]methionine or l-(methyl-2h3)methionine into 2 beta-methyldiplopterol of methylobacterium organophilum and various 3 beta-methylhopanoids of acetobacter pasteurianus ssp. pasteurianus showed that all three hydrogen atoms of the transferred methyl group are retained in the triterpenoids. these methylations are compatible with a methylation substrate such as a delta 2-hopanoid in the case of the 2 beta-methylhopanoid biosynthesis and of a delta 2-hopanoid or sq ...19853926496
effects of detergents and phospholipids on the pyridine nucleotide-independent aldehyde dehydrogenase from membranes of acetobacter rancens.the pyridine nucleotide-independent aldehyde dehydrogenase solubilized and purified from membranes of acetobacter rancens ccm 1774 requires the presence of detergents for activity. while several detergents could stimulate the enzyme activity the stability of the enzyme-detergent complexes was rather low. phospholipid substitution experiments revealed the reversibility of the loss of activity caused by phospholipid removal. enzyme-phospholipid complexes generated from a complex phospholipid fract ...19854084277
[studies on the intensification of the transformation of glycerin to dihydroxyacetone by acetobacter suboxydans]. 19655339218
enzymatic studies on the oxidation of sugar and sugar alcohol. 8. particle-bound l-sorbose dehydrogenase from gluconobacter suboxydans. 19695354025
the pathway of myo-inositol degradation in aerobacter aerogenes. identification of the intermediate 2-deoxy-5-keto-d-gluconic acid. 19714328831
[fractionation of nucleic acids on deae-sephadex a-50]. 19695362443
[characterization of rna-fractions from rat spleens before and after stimulation]. 19695369473
nicotinamide adenine dinucleotide- and nicotinamide adenine dinucleotide phosphate-specific glucose 6-phosphate dehydrogenases of acetobacter xylinum and their role in the regulation of the pentose cycle. 19734144393
[nucleic acid content of cells of acetobacter suboxydans, strain lgu-1]. 19695396616
preparation of radioactive l-glyceraldehyde 3-phosphate. 19695396934
the glucose dehydrogenase activity of the nad-linked glucose-6-phosphate dehydrogenase from acetobacter xylinum. 19734148195
the electron transport system of acetobacter suboxydans with particular reference to cytochrome. 19705504630
kinetic studies on sorbose fermentation. 19705513574
microbial production of d-mannitol and d-fructose from glycerol. 19705535893
pyruvate-phosphate dikinase and the control of gluconeogenesis in acetobacter xylinum. 19715541773
symposium on microbial changes in foods. microbiological aspects of production and spoilage of cider. 19715564383
semiautomated method for microbiological vitamin assays.a semiautomated method for microbiological vitamin assays is described, which includes separate automated systems for the preparation of the cultures and for the measurement of turbidity. in the dilution and dosage unit based on the continuous-flow principle, vitamin samples were diluted to two different dose levels at a rate of 40 per hr, mixed with the inoculated test broth, and dispensed into culture tubes. after incubation, racks with culture tubes were placed on the sampler of an automatic ...19724553802
[on the cyclic alcohol dehydrogenases of acetobacter suboxydans i]. 19675590989
[biochemical oxidation of cyclohexane tetrols and triols and a methoxy-cyclohexanediol]. 19675590990
[6-desoxy-l-idose, 6-desoxy-l-sorbose, and 6-desoxy-l-psicose]. 19675591005
nonfunctional tricarboxylic acid cycle and the mechanism of glutamate biosynthesis in acetobacter suboxydans.acetobacter suboxydans does not contain an active tricarboxylic acid cycle, yet two pathways have been suggested for glutamate synthesis from acetate catalyzed by cell extracts: a partial tricarboxylic acid cycle following an initial condensation of oxalacetate and acetyl coenzyme a. and the citramalate-mesaconate pathway following an initial condensation of pyruvate and acetyl coenzyme a. to determine which pathway functions in growing cells, acetate-1-(14)c was added to a culture growing in mi ...19724640504
activity of fluoro and deoxy analogues of glycerol as substrates and inhibitors of glycerol kinase.analogues of glycerol in which each of the three hydroxy groups is successively replaced by fluorine or hydrogen have been examined as substrates or inhibitors of glycerol kinase (candida mycoderma) to assess the ability of fluorine to mimic a substrate hydroxy group in enzyme-analogue interactions. the four diols resulting from replacement of the hydroxy groups at c-1 or c-2 of sn-glycerol by fluorine or hydrogen are weak substrates. similar substitution of the c-3 hydroxy group gives compounds ...19724655423
[spontaneous mutations in acetic acid bacteria. ii. the meaning of mutations in systematics]. 19675596374
extension of bundles of cellulose microfibrils on agar surfaces by acetobacter xylinum. 19685644414
studies on microbial transformation. xxvi. microbial oxidation of (-)-sparteine. 19734711516
isolation of 5,6-dimethylbenzimidazolyl cobamide coenzyme as a cofactor for glutamate formation from acetobacter suboxydans. 19685683523
[utilization of ethanol by acetomonas oxydans]. 19685727910
[on an acetic acid bacterium which can oxidize acetic acid but cannot use it as sole source of carbon]. 19685727911
[the effect of histones on microorganisms. ii. a study of the process of interaction between histones and acetobacter suboxudans]. 19685733718
determination of urinary polyalcohols by means of gas liquid chromatography. 19685733958
[growth of acetobacter suboxydans on a medium with sorbitol at various values of redox potential]. 19685735973
[composition and various properties of rna in acetobacter suboxydans]. 19685736004
[biochemical dehydrogenations of saccharides. 6. notes on the dehydrogenation of l-arabitol by acetobacter xylinum and on bertrand's rule]. 19734740801
influence of glucose on adenine nucleotide levels and energy charge in acetobacter aceti. 19734764232
induction of orientation of bacterial cellulose microfibrils by a novel terpenoid from acetobacter xylinum.1. the bacterium acetobacter xylinum produces extracellular cellulose microfibrils that form a pellicle in the medium enmeshing the bacterial cells. these microfibrils may show some localized alignment, which can be seen as birefringence when the culture is viewed between crossed polaroid sheets. 2. an increase in birefringence can be induced by the addition of small amounts of certain classes of lipids, particularly sterols, to the cultures. 3. a crude lipid extract from acetobacter cells induc ...19734776865
direct gas chromatographic determination of polyalcohols in biological media. 19695796342
prediction of the course of continuous fermentation on the basis of analysis of the batch process. 19695820744
the dissimilation of glucose and gluconate by acetobacter xylinum. 2. pathway evaluation. 19645834250
the formation of spherulites in pellicles of bacterial cellulose. 19655861284
the nature and mode of action of the cellulolytic component c1 of trichoderma koningii on native cellulose.1. a purified cellulolytic component c(1) was isolated free from associated activities of the cellulase complex and shown to act as a beta-1,4-glucan cellobiohydrolase on both simple and complex forms of native cellulose. 2. the enzyme releases terminal cellobiose units from cellulose, its extent of action being determined principally by the product and by the nature of the substrate. 3. component c(x) of the cellulase system is not required for the action of component c(1) (cellobiohydrolase). ...19734798312
[on the acetic bacteria isolated from grapes]. 19694981161
[enzymatic activity of acetobacter suboxydans. influence of ph and of some substrates on the induction of 2- and 5-ketogenic activity and on growth]. 19645878043
the effect of glucose on the utilization of ethanol by a strain of acetobacter aceti. 19725019325
[on potassium-ammonium antagonism of acetobacter peroxydans]. 19655879800
preparation of specifically labeled d-fructose-14c1. 19655880179
rapid screening assays for soluble and particulate bacterial dehydrogenases. 19674382224
[enzymatic studies of the wild type and of a cellulose-free mutant of acetobacter xylinum]. 19665961232
glutamate biosynthesis in acetobacter suboxydans. vi. formation from acetate plus pyruvate. 19665968575
utilization of glycerol by acetobacter acetigenum under different cultural conditions. 19665969340
the non-spherulitic birefringence in cellulose pellicles of acetobacter xylinum. 19665972644
[constant electrical dipole moment of bacteria and bacteriophages]. 19665999805
[the dehydrogenase activity of cellfree protein extracts of acetobacter suboxydans on the different substrates of oxidation]. 19666004774
[the effect of histones on microorganisms. i. the effect of calf thymus gland histones on acetobacter suboxydans]. 19666005075
variations of 2-ketogluconate and 5-ketogluconate oxidoreductases during growth in acetobacter suboxydans. 19666005320
regulation of hexose phosphate metabolism in acetobacter xylinum.the metabolism of glucose and fructose was studied in resting succinate-grown cells of acetobacter xylinum. from fructose only cellulose and co(2) were formed by the cells, whereas from glucose, gluconate was formed much more rapidly than these two products. the molar ratio of sugar converted into cellulose to sugar converted into co(2) was significantly greater than unity for both hexoses. the pattern of label retention in the cellulose formed by the cells from specifically (14)c-labelled gluco ...19744429547
proceedings: the effect of some single amino acids on the growth of acetobactet aceti. 19744444831
fermentative production of l-sorbose from d-sorbitol by acetobacter suboxydans (vinegar isolate). 19744448494
regulation of gluconeogenesis in acetobacter xylinum. 19725050262
[synthesis of n-mevalonocyl-beta-alanine and its biological activities. v. pantoic acid replacement activities of mevalonic acid on the growth of acetobacter suboxydans]. 19715106292
the induction of birefringence in pellicles of bacterial cellulose from acetobacter xylinum by lipids. 19676036888
[biosynthesis of deuterated bacterial cellulose: study by nmr of incorporation levels and localization of deuterium]. 19715118655
kinetics of glycerol kinases from mammalian liver and candida mycoderma. 19676079771
biphasic growth of acetobacter suboxydans on a glycerol-limiting medium.dihydroxyacetone was quantitatively produced from glycerol during the primary exponential growth phase and depleted during the secondary exponential phase. although no growth was detected on the basal medium, growth occurred upon addition of dihydroxyacetone.19715122812
reactions of transamination and the role of 4-aminobutyrate in acetobacter shüzenbachii. 19826184959
initiation of cellulose biosynthesis. 19715280343
[production of acetic acid with lyophilized and associated strains of acetobacter]. 19715281207
[studies on the systematics and metabolism of acetic acid bacteria]. 19655334787
isocitrate dehydrogenase and glutamate synthesis in acetobacter suboxydans.acetobacter suboxydans is an obligate aerobe for which an operative tricarboxylic acid cycle has not been demonstrated. glutamate synthesis has been reported to occur by mechanisms other than those utilizing isocitrate dehydrogenase, a tricarboxylic acid cycle enzyme not previously detected in this organism. we have recovered alpha-ketoglutarate and glutamate from a system containing citrate, nicotinamide adenine dinucleotide (nad), a divalent cation, pyridoxal phosphate, an amino donor, and dia ...19695361215
stereochemistry of the enzymatic carboxylation of phosphoenolpyruvate. 19695389102
[effect of cultivation conditions on the formation of the calcium salt of 5-ketogluconic acid by acetic acid bacteria]. 19695401102
[ethanol as source of energy but not of carbon in acetomonas oxydans]. 19675591329
[auxotrophism dictated by the source of energy in acetobacter aceti]. 19675591333
the activation of the fad-malic dehydrogenase from acetobacter xylinum by monovalent anions. 19685660686
[comparative characteristics of the dehydrogenase activity of cell-free extracts of some strains of acetobacter suboxydans]. 19685757780
phosphoenolpyruvate carboxylation and aspartate synthesis in acetobacter suboxydans.dialyzed extracts of acetobacter suboxydans atcc 621 catalyze (14)co(2) assimilation in the presence of phosphoenolpyruvate and a divalent cation. the formation of (14)c-oxalacetate was demonstrated and found not to be dependent upon the presence of orthophosphate or diphosphonucleotides. oxalacetate synthesis was stimulated by orthophosphate and inhibited by aspartate. all attempts to demonstrate a reversible carboxylation mechanism have failed. (14)c-aspartate was synthesized when phosphoenolp ...19695773023
role of phosphoenolpyruvate carboxylation in acetobacter xylinum.glucose-grown cells of acetobacter xylinum oxidized acetate only when the reaction mixture was supplemented with catalytic quantities of glucose or intermediates of the citrate cycle. extracts, prepared by sonic treatment, catalyzed the formation of oxalacetate when incubated with phosphoenolpyruvate (pep) and bicarbonate. oxalacetate was not formed in the presence of pyruvate plus adenosine triphosphate. the ability to promote carboxylation of pep was lower in succinate-grown cells than in gluc ...19695788692
biochemical dehydrogenations of saccharides. v. isolation of 5-ketosorbose formed during sorbose fermentation. 19655861553
[enzymatic activity of acetobacter suboxydans. influence of ph on the induction of 5-ketogenic activity]. 19645877161
[effect of the c-source on the growth requirements of acetic acid bacteria]. 19655879799
dna homology and taxonomy of pseudomonas and xanthomonas. 19665922298
glutamate biosynthesis in an organism lacking a krebs tricarboxylic acid cycle. v. isolation of alpha-hydroxy-gamma-ketoglutarate (hkg) in acetobacter suboxydans. 19666005666
[studies on sorbose fermentation in a batch and continuous cultures]. 19666012785
the oxidation of d-quinate and related acids by acetomonas oxydans.1. growing cells of a small number of strains of acetomonas oxydans oxidized d-quinate to 5-dehydroquinate. 2. d-shikimate was oxidized to 4,5-dihydroxy-3-oxocyclohex-1-ene-1-carboxylate (3-dehydroshikimate, formerly 5-dehydroshikimate). 3. d-dihydroshikimate was oxidized to the corresponding 5-dehydro compound, but epidihydroshikimate oxidation by growing cells was not observed. 4. cell-free extracts oxidized d-quinate to 5-dehydroquinate with the consumption of the stoicheiometric amount of ox ...19676030289
the extracellular proteins of acetobacter xylinum and their relationship to cellulose synthesis. 19676033822
biosynthesis of alpha-isopropylmalic and citric acids in acetobacter suboxydans.cell-free extracts of acetobacter suboxydans were prepared which were capable of condensing alpha-ketoisovalerate with (14)c-labeled acetyl-coenzyme a to yield (14)c-labeled alpha-isopropylmalate. the product of the reaction was isolated by paper and column chromatography and was characterized by recrystallization with synthetic alpha-isopropylmalic acid to constant specific radioactivity. the formation of alpha-isopropylmalate by extracts of a. suboxydans plus the ability of the organism to gro ...19676035258
[regulation of citrate synthase in facultative methylotrophic bacteria].commonly the tca cycle fulfils an anabolic and a catabolic function in case of aerobic chemoorganoheterotrophic nutrition. in methylotrophic growth the tca cycle is dispensable as a bioenergetic pathway. this is reflected by properties of citrate synthase in facultative methylotrophic bacteria. two citrate synthases, a "chemoorganoheterotrophic" one, which is inhibited by nadh (or atp in acetobacter mb 58), and a "methylotrophic" one, which is not or less affected by energy indicators, were foun ...19836880250
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