| [biotransformation of cycloartane-type triterpenoid from myrrh]. | to study the biotransformation of cycloartan-24-ene-1alpha,2alpha, 3beta-triol isolated from myrrh and find new antitumor bioactive cycloartane-type derivatives. | 2012 | 23252274 |
| cloning of exoinulinase gene from penicillium janthinellum strain b01 and its high-level expression in pichia pastoris. | the aim of this study is to improve exoinulinase production by expression of a cloned exoinulinase gene inua1 (genbank accession no. jf961344) from penicillium janthinellum strain b01 in pichia pastoris. | 2011 | 21895898 |
| comparative production of cellulases by mutants of penicillium janthinellum ncim 1171 and its application in hydrolysis of avicel and cellulose. | mutants of penicillium janthinellum ncim 1171 were evaluated for cellulase production using both submerged fermentation (smf) and solid state fermentation (ssf). mutant eu2d-21 gave highest yields of cellulases in both smf and ssf. hydrolysis of avicel and cellulose were compared using smf and ssf derived enzyme preparations obtained from eu2d-21. surprisingly, the use of ssf derived preparation gave less hydrolysis compared to smf derived enzymes. this may be due to inactivation of β-glucosidas ... | 2011 | 21300541 |
| enzymatically synthesized polyaniline layer for extension of linear detection region of amperometric glucose biosensor. | in this article a new method for fabrication of enzymatic electrodes suitable for design of amperometric glucose biosensor and/or anode of biofuel cell powered by glucose is presented. glucose oxidase (gox) e.c. 1.1.3.4. from penicillium vitale was immobilized on the carbon rod electrode by cross-linking it with glutaraldehyde (gox-electrode). catalytic activity of immobilized gox was exploited for polymerisation of aniline by taking a high concentration of hydrogen peroxide produced during the ... | 2010 | 20638831 |
| [effects of pre-treatment on cu2+ absorption of penicillium janthinellum strain gxcr]. | in order to effectively increase capacity of cu2+ absorption by penicillium from cu2+-containing aqueous solution and to study the mechanisms of absorption, effects of eight pre-treatment methods on cu2+ absorption of penicillium janthinellum strain gxcr were compared. the results showed that the efficiency of cu2+ absorption obviously increased through pre-treatment by homogenization, homogenization-basification (naoh), oven dry (80 degrees c), homogenization-salinification (nacl), homogenizati ... | 2009 | 19441230 |
| [cu and fe bioleaching in low-grade chalcopyrite and bioleaching mechanisms using penicillium janthinellum strain gxcr]. | bioleaching of cu and fe in low-grade chalcopyrite using penicillium janthinellum strian gxcr was studied. as a result, shaking bioleaching was more efficient than submerged bioleaching; cu bioleaching was much better than fe bioleaching; under conditions of optimum carbon source (10% sucrose, w/v), optimum nitrogen source (1.5% nano3, w/v), shaking bioleaching and the optimum combination of conditions (initial ph 6.0 in leaching media, 5% (w/v) 200-mesh ore and initial inocula of 3.0x10(5) coni ... | 2008 | 19256351 |
| xylanase recovery by ethanol and na2so4 precipitation. | xylans are the major components of the hemicellulosic fraction of lignocellulosic biomass and their hydrolysis can be obtained using xylanases from penicillium janthinellum. in this work, sugarcane bagasse hemicellulosic hydrolysate was used as the substrate for producing xylanase. the precipitation of these enzymes was studied using ethanol and na2so4 as precipitating agents. ethanol precipitation experiments were performed batchwise in concentrations ranging from 10 to 80%, ph 4.0 to 7.0, at 4 ... | 1998 | 18576030 |
| xylanase recovery. effect of extraction conditions on the aqueous two-phase system using experimental design. | the partitioning of xylanase produced by penicillium janthinellum in aqueous two-phase systems (atps) using poly(ethylene glycol) (peg) and phosphate (k2hpo4/kh2po4) was studied employing a statistical experimental design. the aim was to identify the key factors governing xylanase partitioning. the interactions of five factors (peg concentration molecular weight, concentration of buffer k2hpo4/kh2po4, ph, and nacl concentration) and their main effects on the partition coefficient (k) were evalua ... | 1998 | 18576027 |
| strain improvement of penicillium janthinellum ncim 1171 for increased cellulase production. | the strain of penicillium janthinellum ncim 1171 was subjected to mutation involving treatment of ethyl methyl sulfonate (ems) for 24h followed by uv-irradiation for 3min. successive mutants showed enhanced cellulase production (ems-uv-8), clearance zone on avicel containing plate (sm2) and rapid growth on walseth cellulose agar plates containing 0.2% 2-deoxy-d-glucose (sm3). these mutants were transferred to walseth cellulose plates containing higher concentration (1.5%) of 2-deoxy-d-glucose (s ... | 2007 | 17097876 |
| fungal colonization of soil-buried plasticized polyvinyl chloride (ppvc) and the impact of incorporated biocides. | plasticized polyvinyl chloride (ppvc) with or without incorporated biocides was buried in grassland and forest soil for up to 10 months. the change with time in viable counts of fungi on the plastic surface was followed, together with the percentage capable of clearing the two plasticizers dioctyl adipate (doa) and dioctyl phthalate (dop). with time fungal total viable counts (tvc) on control ppvc increased and the fraction able to clear doa was considerably higher than the average estimated in ... | 2006 | 16735736 |
| [catalase activity as affected by carnosine and sodium nitrite in vitro]. | it was shown in vitro that the activity of catalase penicillium vitale decreases when treated by sodium nitrite to the greater extent than when affected by dipeptide carnosine (beta-alanyl-l-histidine). at alternating introduction of carnosine and nano2 that component affected the catalase activity which was the first to be introduced. the entering of the next metabolite into the medium did not change the enzyme activity. it is shown that carnosine binds with a molecule of catalase. carnosine ma ... | 2015 | 16100910 |
| extractive cultivation of xylanase by penicillium janthinellum in a poly(ethylene glycol)/cashew-nut tree gum aqueous two-phase system. | cultivation of the fungus penicillium janthinellum for xylanase production was studied in a poly(ethylene glycol)/cashew-nut tree gum aqueous two-phase system, using a two-level fractional factorial design. the parameters studied were initial ph, cultivation time, type of agro-industrial residue (oat husk or corn cob), agitation, temperature, and phase-forming polymers. the xylanase produced during fermentation partitioned into the top phase. the agitation and temperature (negative), cultivation ... | 2015 | 15575727 |
| in vitro expression of penicillium janthinellum cellobiohydrolase i gene in a coupled transcription-translation system. | an enzymatically-active fungal cellobiohydrolase i (cbh i) was first synthesized in a coupled reticulocyte lysate system lacking of glycosylation modification by the template dna(cbh1) in the presence of t7 rna polymerase. the synthesized cbh i had the expected size (57 kda) and catalyzed the substrate of p-nitrophenyl-beta-d-cellobioside (pnpc), and had no activity against carboxymethyl cellulose (cmc-na). the k(m) and v(max) values of the cbh i for pnpc were 0.82 mmol and 0.067 micromol min(-1 ... | 2000 | 10989180 |
| partitioning of xylanolitic complex from penicillium janthinellum by an aqueous two-phase system. | this work evaluates the influences of five parameters (ph, peg molecular mass, peg concentration, concentration of buffer k2hpo4-kh2po4 and nacl concentration) on xylanolitic complex partitioning produced by p. janthinellum in aqueous two-phase systems, using a 2(5) factorial experimental design. a mathematical model to quantify the influence of these parameters was attained and statistically tested. the optimum point for total protein extraction was obtained under the following conditions: ph 7 ... | 2000 | 10942304 |
| [taxonomic position and nitrogen-containing secondary metabolites of the fungus penicillium vitale pidoplichko et bilai apud bilai]. | the type strain penicillium vitale pidoplichko et bilai apud bilai 1961 vkm f-3624 was found to considerably differ from a sibling species p. janthinellium (syn. p. simplicissimum) in some physiological and morphological features (growth rates at different temperatures, the size of philiades, and the shape of conidia), as well as in the pattern of the nitrogen-containing secondary metabolites produced (roquefortine, 3,12-dihydroroquefortine, meleagrin, aurantioclavine, indole-3-acetic acid, and ... | 2013 | 10920814 |
| beta-xylosidase recovery by reversed micelles. use of cationic surfactant. | beta-xylosidase, an enzyme produced by penicillium janthinellum fungus, was prepurified by fractionated precipitation with ethanol and extracted by reversed micelles of n-benzyl-n-dodecyl-n-bis(2-hydroxyethyl) ammonium chloride (bdbac) cationic surfactant. a 2(5-1) fractional factorial design was employed to evaluate the influence of the following factors on the enzyme extraction: ph (a), conductivity (b), surfactant concentration (c), cosolvent concentration (d) and temperature (e). a statistic ... | 2000 | 10849861 |
| optimization of pyrene oxidation by penicillium janthinellum using response-surface methodology. | at present, there is little information on the optimization of the degradation of polycyclic aromatic hydrocarbons (pah) by deuteromycete filamentous fungi, a reaction catalyzed by cytochrome p450 monooxygenases. we utilized response-surface methodology to determine the optimal growth conditions for the oxidation of the pah pyrene by penicillium janthinellum sfu403, with respect to the variables glucose concentration, nitrate concentration and bioconversion time. models were derived for the rela ... | 1999 | 10341435 |
| pyrene is metabolized to bound residues by penicillium janthinellum sfu403. | we have previously shown that the filamentous fungus, penicillium janthinellum sfu403 (sfu403) oxidizes pyrene to pyrene 1,6- and 1,8-quinones and that the level of pyrenequinones (pqs) subsequently declines suggesting that pqs are not terminal metabolites. the purpose of this study was to determine the fate of pqs in sfu403. first, we compared the fate of 14c-pyrene in sfu403 and a non-pyrene-oxidizing fungus, a paecilomyces sp.. after 7 days of incubation, more than 80% of the radioactivity wa ... | 2000 | 11487060 |
| inactivation of mucor plumbeus by the combined actions of chitinase and high hydrostatic pressure. | sporangiospores were treated with high hydrostatic pressure and/or fungal chitinase in order to study the inhibition of germination and growth of the food spoiling mold mucor plumbeus. total fungal inhibition was obtained either at 4.0 kbar or by 10 u/ml of chitinase from penicillium janthinellum. a pretreatment with 1 u/ml of the same chitinase reduced the pressure necessary to obtain complete spore inhibition to 3 kbar. | 1999 | 10573398 |
| endophytic paecilomyces formosus lhl10 augments glycine max l. adaptation to ni-contamination through affecting endogenous phytohormones and oxidative stress. | this study investigated the ni-removal efficiency of phytohormone-producing endophytic fungi penicillium janthinellum, paecilomyces formosus, exophiala sp., and preussia sp. among four different endophytes, p. formosus lhl10 was able to tolerate up to 1 mm ni in contaminated media as compared to copper and cadmium. p. formosus lhl10 was further assessed for its potential to enhance the phytoremediation of glycine max (soybean) in response to dose-dependent increases in soil ni (0.5, 1.0, and 5.0 ... | 2017 | 28611799 |
| penicillium janthinellum in sputum and bronchoalveolar lavage in an aids patient with pneumonia. | | 1997 | 11864114 |
| [the kinetic and catalytic properties of penicillium vitale catalase]. | the steady-state kinetics of catalytic action of penicillium vitale catalase has been studied. the enzyme reaction conforms to the michaelis-menten equation, which is shown by considering the initial velocity of the enzyme-catalytic reaction with increased concentrations of hydrogen-peroxide and sodium perborate. the parameter km value is rather large (231-259) mm. on the other hand the pen, vitale catalase is one of the more active enzymes and shows kcat values equal to 0.8-3.0 x 10(-6) s-1 and ... | 2015 | 9005665 |
| novel serine penicillocarboxypeptidase cpd-s3 from penicillium janthinellum ibt 3991: purification, characterization, and uses in peptide synthesis and modification. | a novel carboxypeptidase (cpd-s3) from penicillium janthinellum ibt 3991 has been isolated in a two-step purification procedure by cation exchange and affinity chromatography. the enzyme is a serine carboxypeptidase with a denatured molecular mass determined by sds of 62 kda of which 32% is carbohydrate. the isoelectric point is 5.1. cpd-s3 exhibits a high stability towards organic solvents and elevated temperatures. besides the carboxypeptidase activity, cpd-s3 exhibits esterase, amidase, and c ... | 1993 | 7764295 |
| the primary structure of carboxypeptidase s1 from penicillium janthinellum. | the complete amino acid sequence of carboxypeptidase s1 from penicillium janthinellium has been determined by n-terminal sequencing of the reduced and vinylpyridinated protein and of peptides obtained by cleaved with cyanogen bromide, iodosobenzoic acid, hydroxylamine, endoproteinase lysc, endoproteinase aspn and glu-specific proteinase from b. licheniformis. the enzyme consists of a single peptide chain of 433 amino acid residues and contains 9 half-cystine residues and one glycosylated asparag ... | 1993 | 8224168 |
| [identification of toxigenic mould in soft drink causing food poisoning]. | in a soft drink caused food poisoning, white floccus was found and mould count was 6.0 x 10(2) cfu/ml. the mycoflora was made of only one kind of mould which was identified as penicillium janthinellum biourge. this isolate can grow under anaerobic condition. the culture liquid of the isolate was fed to mice orally for toxicity test, which made the mice lose weight. an extract of the culture liquid was tested in weaned mice inaberitoneally for toxicity and all mice died in 24h. the toxic symptoms ... | 1992 | 1606874 |
| carboxypeptidase s-1 from penicillium janthinellum: enzymatic properties in hydrolysis and aminolysis reactions. | carboxypeptidase s-1 from penicillium janthinellum has been isolated by affinity chromatography and characterized. the enzyme activity is unusually stable in organic solvents, e.g. 80% methanol. the hydrolysis of peptide substrates is apparently dependent on three ionizable groups. one group, with pka of 4.0-4.5, is a catalytically essential residue in its deprotonated form, and another group with a pka of 6.5-7.0 functions in its protonated form, apparently as the binding site for the c-termina ... | 1988 | 3256309 |
| three-dimensional structure of catalase from penicillium vitale at 2.0 a resolution. | the three-dimensional structure analysis of crystalline fungal catalase from penicillium vitale has been extended to 2.0 a resolution. the crystals belong to space group p3(1)21, with the unit cell parameters of a = b = 144.4 a and c = 133.8 a. the asymmetric unit contains half a tetrameric molecule of 222 symmetry. each subunit is a single polypeptide chain of approximately 670 amino acid residues and binds one heme group. the amino acid sequence has been tentatively determined by computer grap ... | 1986 | 3712443 |
| release of cellulases from penicillium janthinellum. | | 1986 | 18553855 |
| penicillopepsin, the aspartic proteinase from penicillium janthinellum: substrate-binding effects and intermediates in transpeptidation reactions. | | 1985 | 3912235 |
| [study of the subunit structure of catalase from penicillium vitale]. | a molecule of penicillium vitale catalase is shown to dissociate into subunits with the molecular weight 75-80 kdalton. when hemin is splitted off the molecule also disintegrates into subunits equalling 1/4 of the enzyme molecule. the amino acid composition and fingerprints of the catalase subunits were studied. it is supposed that n-terminal residue of the subunit is blocked. | 2015 | 4035792 |
| [application of ultrafiltration for concentration and purification of penicillium vitale catalase]. | various factors are studied for their effect on the ultrafiltration of penicillium vitale catalase. it is established that acetate cellulose and polyamide membranes may be used for additional purification and deep concentration of native preliminarily purified enzyme solutions. membranes yam-300 and yam-450 are most preferable. at the temperature of 10 degrees c, pressure 0.2 mpa and 100-fold concentration of the catalase solution the enzyme yield at the ultrafiltration stage is 96-100%. | 2015 | 6636309 |
| repression of endo-1,4-beta-glucanase formation in penicillium janthinellum and product inhibition of its 1,4-beta-glucanases and cellobiases. | endo-1,4-beta-glucanase formation of penicillium janthinellum was repressed by glucose, sophorose, and glycerol. chromatography on deae-sephadex a-50 was employed to separate the 1,4-beta-glucanases from two cellobiases. the 1,4-beta-glucanases were inhibited competitively by cellobiose and glucose, and the two cellobiases were inhibited by glucose and glucono-delta-lactone. | 1982 | 6799497 |
| [stability of penicillium vitale immobilized catalase in continuous decomposition of hydrogen peroxide]. | the process of hydrogen peroxide continuous decomposition by the preparation of the fungus penicillium vitale catalase immobilized by aminoorganosilica which were activated by glutaric aldehyde, cyanuric chloride or 2,4-toluylene diisocyanate. catalase with an oxidized carbohydrate component was used as well. such a modified enzyme was directly bound with the surface of aminocontaining silica and alumina. it is shown that in the process of h2o2 decomposition the preparations of immobilized catal ... | 2015 | 7281255 |
| [immobilization of penicillium vitale catalase on aminoethyl cellulose and properties of the obtained preparations]. | preparations of penicillium vitale catalase immobilized by aminoethyl cellulose (ae-cellulose) are obtained using two methods: by the enzyme covalent cross-linking with the carrier by glutaric aldehyde and by the covalent binding of catalase to the carrier aminogroups through the carbohydrate enzyme component. a dependence is established for the degree of catalase binding and catalase activity of the immobilized enzyme on the enzyme carrier in immobilization ratio. the optimal enzyme-carrier rat ... | 2015 | 7281254 |
| [immobilization of penicillium vitale glucose oxidase by aminoethyl cellulose and properties of immobilized enzyme]. | penicillium vitale glucose oxidase modified by oxidation of the carbohydrate component is in a covalent combination with aminoethyl cellulose (ae-cellulose). with the optimal enzyme: carrier ratio the manifested activity of glucose oxidase in the preparation is 4.3 +/- 0.8% of the attached enzyme activity. it is established that thermostability, stability to an inactivating effect of a labilizing fraction and ph-stability with ph alkaline values in the immobilized glucose oxidase are higher than ... | 2015 | 7281253 |
| formation and location of 1,4-beta-glucanases and 1,4-beta-glucosidases from penicillium janthinellum. | formation and location of 1,4-beta-glucanases and 1,4-beta-glucosidases were studied in cultures of penicillium janthinellum grown on avicel, sodium carboxymethyl cellulose, cellobiose, glucose, mannose, and maltose. endo-1,4-beta-glucanases were found to be cell free, and their formation was induced by cellobiose. 1,4-beta-glucosidases, on the other hand, were formed constitutively and were primarily cell free, but with a small amount strongly associated with the cell wall. low 1,4-beta-glucosi ... | 1981 | 16345751 |
| [comparative kinetics of reactions catalyzed by glucose oxidase in the presence of different electron acceptors]. | it was shown that six redox indicators, beside oxygen, can be used as substrates for glucose oxidase from penicillium vitale. the ph dependence of the rate of glucose oxidase-catalyzed reactions in the presence of oxygen and artificial electron acceptors was studied. in contrast to the reaction involving oxygen, in which the maxima of the ph activity profile were observed at ph 5.6, glucose oxidase reveals maximal ph activity profile at ph 7.5 -- 7.6 in the presence of phenasine methosulfate, ba ... | 1981 | 7284485 |
| growth of penicillium janthinellum on glycine as sole carbon and nitrogen source. | penicillium janthinellum is able to grow on glycine as the sole carbon and nitrogen source. the amino acid is transaminated to glyoxylate which is further metabolised to pyruvate by the glycerate pathway. the reaction product of partially purified glycerate kinase from this fungus is 2-phosphoglycerate. phosphoglycerate mutase initiates gluconeogenesis from glycine. partially purified phosphoglycerate mutase is inhibited by fructose 6-phosphate. the possible significance of this regulation is di ... | 1980 | 6251917 |
| [formation of coenzyme vitamins and flavin-adenine dinucleotide during the growth of penicillium vitale pidopl. et bilai]. | | 2006 | 7432204 |
| [immobilization of penicillium vitale pidopl. et bilai catalase by inorganic carriers]. | an efficient method is developed for p. vitale catalase immobilization through the oxidized carbohydrate enzyme component, using silochrome. the method provides the enzyme binding without losing its catalytic capacity in the immobilized preparation. when the enzyme is immobilized by high-dispersed silica containing isocyanate, aldehyde groups or active atoms of chlorine, 8, 15, and 20 mg of the enzyme is bounded per 1 g of the carrier, respectively, its catalytic capacity being completely retain ... | 2015 | 6266097 |
| [effect of microelements on growth of penicillium vitale pidopl. et bilai and synthesis of a number of extracellular enzymes]. | | 2006 | 7402104 |
| [immobilization of penicillium vitale glucose-oxidase on aminosilochrome and properties of immobilized enzyme]. | penicillium vitale glucose-oxidase modified by means of the carbohydrate component oxidation is added covalently to aminoorganosylochrome. the activity of the immobilized preparations is 20-38% depending on the protein-carrier ration in immobilization. comparison of some properties of native and immobilized glucose-oxidase showed that the rh optimum of the immobilized glucose-oxidase is slightly widened towards the alkaline regions; the immobilized glucose-oxidase possesses a considerably higher ... | 2015 | 38549 |
| [total activity of glucose oxidase, catalase and invertase and their distribution in the mycelial subcellular fractions of penicillium vitale pidopl. et bilai]. | | 2006 | 32465 |
| purification & properties of an extracellular dextranase from penicillium janthinellum. | | 1978 | 748164 |
| [stabilization of modified glucose oxidase from penicillium vitale incorporated into the polymeric chains of gels]. | glucose oxidase from penicillium vitale was modified by unsaturated compounds, e.g. acrolein, allylisothiocyanate, acryloyl chloride and maleic anhydride. the degree of modification for the respective agents made up to 27.2, 8.3, 11.1 and 35.0% of the amine residues; the enzymatic activity was thereby retained by 98, 100, 0.03 and 58%, respectively. the thermal stability of modified enzymes was decreased 2-7 times. the modified preparations were copolymerized with acrylamide or 2-hydroxyethyl me ... | 1978 | 656485 |
| [ultrastructure of penicillium vitale pidopl. et bilai--producer of catalase and glucose oxidase]. | | 2006 | 604723 |
| [natural variability of penicillium vitale pidopl. et bilai and characteristics of active variants of the fungus that produce glucose oxidase]. | | 2008 | 916914 |
| [stabilizing effect of calcium ions on glucose oxidase of penicillium vitale]. | reconstruction of p. vitale glucose oxidase from apeonzyme and coenzyme (fad) was studied as affected by iodine acetate as well as mercury and calcium ions. mercury ions, iodine acetate as well as the labilizing fraction (flavin adenine-containing component) are established to inhibit the reconstruction affecting the sulphydryl groups of the apoenzyme which take part in addition of fad to it. calcium ions prevent the effect of the "labilizing" fraction, iodine acetate and mercury ions on the glu ... | 2013 | 888220 |
| [dissociation of penicillium vitale catalase under the effect of urea and acid ph]. | conditions are studied for penicillium vitale catalase dissociation into subunits under the effect of urea (0.7-8.5 m) and acid ph (5.0-2.0). in 8.0 m urea (ph 5.0) a molecule of the p. vitale catalase dissociates with formation of the components, the sedimentation coefficient of which is 2.4+/-0.2s, the molecular weight is 153000+/-2800. dissociation at ph 2.2 in 4.0 m urea results in formation of components with the sedimentation coefficient 2.2+/-0.3 s. the catalase molecule dissociation unde ... | 2013 | 18833 |
| [mechanism of labilization of penicillium vitale glucose oxidase]. | the article deals with conditions for splitting the penicillium vitale glucosooxidase molecule into apoenzyme and coenzyme, for reconstruction of the enzyme from apoenzyme and fad as well as for the effect of some factors ("labilizing" fraction, dithiotreitol) on it. specific activity of the reconstructed enzyme is on the average 85% of the initial enzyme specific activity: "the labilizing" fraction inhibits reconstruction of glucosooxidase from apoenzyme and fad, that is due to oxidation of the ... | 2008 | 867542 |
| [comparative evaluation of the enzymatic activity of the mycelial homogenates from penicillium vitale pidopl. et bilai broken down by different methods]. | | 2006 | 994870 |
| action of crystalline acid carboxypeptidase from penicillium janthinellum. | acid carboxypeptidase (ec 3.4.12.-) crystallized from culture filtrate of penicillium janthinellum has been investigated for its use in carboxy-terminal sequence determination of z-gly-pro-leu-gly, z-gly-pro-leu-gly-pro, angiotensin i, native lysozyme, native ribonuclease t1, and reduced s-carboxy-methyl-lysozyme. the examination indicated that proline and glycine were liberated from z-gly-pro-leu-gly-pro. at high enzyme concentration, the enzyme catalyzed complete sequential release of amino ac ... | 1975 | 239751 |
| [comparative characteristics of catalase from the fungus penicillium vitale, which is synthesized under different nutritional conditions]. | a comparative study of properties (absorption spectra, thermostability, ph optimum, polyacrylamide gel electrophoresis, deae-cellulose separation) and structure (amino acid composition, finger-prints, carbohydrate composition) was performed for p. vitale catalase synthesized under different medium conditions. in all cases the results were similar. the only difference occured in the amount of synthesized proteins. a conclusion is drawn that under different nourishing conditions of the fungus the ... | 2006 | 3004 |
| [variability in penicillium janthinellum biourge, a producer of the antibiotic janthinellin, under the action of nitrosomethylurea]. | variation of the janthinellin-producing organism p. janthinellum was induced by nitrozomethylurea (nmu). the following concentrations of nmu were tested: 0.5; 0.25, 0.125 per cent at the exposure time of 15 minutes, 1 and 10 hours. the conidia survival had back dependence on the concentration and exposure time. the morphological variation was evident from the presence of forms with changed colour of the colony surface mycelium, light green, brown, light yellow, yellow-pink and white conidia and ... | 1975 | 1211902 |
| purification and properties of an extracellular acid ribonuclease from penicillium janthinellum. | | 1974 | 4371002 |
| [variability of penicillium janthinellum biourge--producer of the antibiotic janthinellin and study of the nuclei during ontogenesis of the fungus]. | | 2008 | 4453214 |
| [carbohydrate components of the glucose oxidase from penicillium vitale]. | | 2013 | 4441570 |
| [study of the amino acid makeup of the proteins in the mycelial pellicle of penicillium vitale pid. et bil]. | | 2006 | 4840331 |
| [hydrodynamic properties and molecular weight of penicillium vitale catalase]. | | 2016 | 4823742 |
| [study of tubular crystals of penicillium vitale glucose oxidase and its quaternary structure]. | | 1973 | 4754779 |
| influence of inorganic nitrate on the formation of extracellular protease and ribonuclease by penicillium janthinellum. | | 1973 | 4762798 |
| [composition and properties of the catalase from penicillium vitale pidopl. et bilai]. | | 2000 | 4790749 |
| [obtaining purified preparations of catalase from the fungus penicillium vitale pidopl. et bilai]. | | 1972 | 4661073 |
| [conditions of direct biosynthesis of catalase by penicillium vitale pidopl. et bilai]. | | 2001 | 5153535 |
| [the effect of the quality of the sowing material on the enzyme activity and flavinogenesis of penicillium vitale pidopl. et bilai under industrial conditions]. | | 2015 | 5153983 |
| [composition and structure of glucose oxidase from penicillium vitale]. | | 2013 | 5556037 |
| [role of inoculum in formation of glucose oxidase and catalase of the penicillium vitale fungus]. | | 2000 | 5519073 |
| large-scale preparation and some properties of penicillopepsin, the acid proteinase of penicillium janthinellum. | | 1970 | 5418964 |
| a crystalline proteinase (peptidase a) from penicillium janthinellum: preliminary x-ray data. | | 1969 | 5346053 |
| [natural variability of the strain penicillium janthinellum biourge--producer of janthinellin]. | | 1968 | 5707360 |
| [glucosooxidase from penicillium vitale pidopl. and bilai]. | | 2000 | 5733674 |
| a pepsin-like enzyme from penicillium janthinellum. | | 1968 | 4866867 |
| the role of a protease in sporulation of penicillium janthinellum. | | 1966 | 5961655 |
| [on the mechanism of the stimulatory effect of calcium carbonate on the glucose oxidase and catalase activities of penicillium vitale]. | | 2013 | 5871568 |
| [on some properties of crystalline and purified non-crystalline glucose-oxidase preparations from penicillium vitale pidopl. et bilai]. | | 1965 | 5869922 |
| proteolytic enzymes of penicillium janthinellum. ii. properties of peptidase b. | | 1964 | 14264888 |
| proteolytic enzymes of penicillium janthinellum. i. purification and properties of a trypsinogen-activating enzyme (peptidase a). | | 1964 | 14264887 |
| [isolation of glucose oxidase from penicillium vitale pidopl. et bilai]. | | 1964 | 14335573 |
| [iantinellin--an antibiotic with antifungal properties produced from penicillium janthinellum biourge]. | | 1963 | 13970363 |
| [on the identity of glucose oxidase and microcid from a new type of penicillium vitale]. | | 2007 | 14475320 |
| [an industrial method for the purification and crystallization of and some properties of glucose oxidase from the fungus penicillium vitale pidopl. et bilai]. | | 1962 | 13902922 |
| [formation of beta-fructofuranosidase by penicillium vitale pidopl. et bilai and other species of the genus penicillium lk]. | | 2006 | 1219324 |
| [preparation in crystalline form of catalase from penicillium vitale pidopl. et bilai]. | | 1975 | 1204470 |
| [industrial experiment in obtaining catalase from penicillium vitale pidopl. et bilai]. | | 2006 | 11395 |