RESUMO
A R-stereospecific amidase was purified from Brevibacterium epidermidis ZJB-07021 and characterized in detail. The amidase was purified to homogeneity by three chromatographic steps for up to 328.9-fold with specific activity of 31.9 U mg(-1). The enzyme was a homodimer with a molecular mass of 94 kDa. It exhibited maximum activity at 40 °C and pH 7.5. The enzyme was strongly inactivated by serine protease inhibitor PMSF. The values of Km and Vmax for racemic 2,2-dimethylcyclopropane carboxamide (DMCPCA) were 4.58 mM and 35.03 µmol min(-1) mg(-1) protein, respectively. The amidase showed a broad substrate spectrum toward aliphatic, aromatic and heterocyclic amides, but could hardly hydrolyze the bulky side-chain-containing amides. Furthermore, kinetic resolution of racemic DMCPCA by the amidase afforded S-DMCPCA in 46.3% yield and 99% ee with an average E-value of 67. These unique properties of the amidase imply that it is a promising biocatalyst for the production of chiral amides and carboxylic acids.
Assuntos
Amidoidrolases/isolamento & purificação , Amidoidrolases/metabolismo , Brevibacterium/enzimologia , Ciclopropanos/química , Ciclopropanos/metabolismo , Concentração de Íons de Hidrogênio , Cinética , Metais/farmacologia , Estereoisomerismo , Especificidade por Substrato , TemperaturaRESUMO
A combination of microbial strain improvement and statistical optimization is investigated to maximize echinocandin B (ECB) production from Aspergillus nidulans ZJB-0817. A classical sequential mutagenesis was studied first by using physical (ultraviolet irradiation at 254 nm) and chemical mutagens (lithium chloride and sodium nitrite). Mutant strain ULN-59 exhibited 2.1-fold increase in ECB production to 1583.1 ± 40.9 mg/L when compared with the parent strain (750.8 ± 32.0 mg/L). This is the first report where mutagenesis is applied in Aspergillus to improve ECB production. Further, fractional factorial design and central composite design were adopted to optimize the culture medium for increasing ECB production by the mutant ULN-59. Results indicated that four culture media including peptone, K2HPO4, mannitol and L-ornithine had significant effects on ECB production. The optimized medium provided another 1.4-fold increase in final ECB concentration to 2285.6 ± 35.6 mg/L compared to the original medium. The results of this study indicated the combined application of a classical mutation and medium optimization can improve effectively ECB production from A. nidulans and could be a promising tool to improve other secondary metabolites production by fungal strains.
Assuntos
Aspergillus nidulans/fisiologia , Técnicas de Cultura Celular por Lotes/métodos , Meios de Cultura/metabolismo , Equinocandinas/biossíntese , Proteínas Fúngicas/biossíntese , Melhoramento Genético/métodos , Mutagênicos/farmacologia , Aspergillus nidulans/efeitos dos fármacos , Aspergillus nidulans/efeitos da radiação , Equinocandinas/genética , Proteínas Fúngicas/genética , Mutação/efeitos dos fármacos , Mutação/genética , Mutação/efeitos da radiação , Especificidade da Espécie , Raios UltravioletaRESUMO
Echinocandin B (ECB), an echinocandin type of lipopeptide antibiotic produced by Aspergillus nidulans, is a precursor for the synthesis of novel anti-fungal drug - anidulafungin. In this work, a separation strategy involving one-step macroporous resin adsorption chromatography was established for ECB purification from Aspergillus nidulans CCTCC M 2010275 fermentation broth. Among nine macroporous resin adsorbents tested, the non-polar resin HP-20 had the best adsorption and desorption performance. The static equilibrium adsorption data fitted well with the Langmuir equation, and the adsorption kinetic followed the pseudo-second order model. The separation parameters of ECB from broth were optimised by dynamic adsorption/desorption experiments with the column packed with HP-20 resin. Under optimal conditions, the purity increased by 3.8-fold from 23.2% in broth to 88.5% in eluent with 87.1% recovery yield by a one-step treatment. Our study provided a one-step and effective method for large-scale production of ECB, and offered references for separating other echinocandins from broth.
Assuntos
Aspergillus nidulans/metabolismo , Cromatografia de Afinidade/métodos , Equinocandinas/isolamento & purificação , Proteínas Fúngicas/isolamento & purificação , Adsorção , Equinocandinas/química , Equinocandinas/metabolismo , Proteínas Fúngicas/química , Proteínas Fúngicas/metabolismoRESUMO
BACKGROUND: Maleimides, both natural and synthesised, have good biological activities. In a continuous effort to discover new maleimides with good antifungal activities, the authors have synthesised a series of 3,4-dichloro-, 3-methyl and non-substituted maleimides based on previous studies. The compounds were biologically evaluated against the fungal pathogen Sclerotinia sclorotiorum. RESULTS: Of the 63 compounds evaluated, 25 compounds had interesting inhibitory potency with EC50 < 10 µg mL(-1). N-(3,5-Dichlorophenyl)-3,4-dichloromaleimide (EC50 = 1.11 µg mL(-1)) and N-octyl-3-methylmaleimide (EC50 = 1.01 µg mL(-1)) were more potent than the commercial fungicide dicloran (EC50 = 1.72 µg mL(-1)). The results showed that compounds exhibiting log P values within the range 2.4-3.0 displayed the best results in terms of fungicidal activity, and this seemed, therefore, to be the optimum range for this physicochemical parameter. CONCLUSION: The present work demonstrates that some maleimides can be used as potential lead compounds for developing novel antifungal agents against S. sclerotiorum.
Assuntos
Fungicidas Industriais/farmacologia , Maleimidas/farmacologia , Antifúngicos/síntese química , Antifúngicos/farmacologia , Ascomicetos/efeitos dos fármacos , Fungicidas Industriais/síntese química , Maleimidas/síntese química , Testes de Sensibilidade Microbiana , Relação Estrutura-AtividadeRESUMO
(S)-4-chloro-3-hydroxybutanoate ((S)-CHBE) is an important chiral intermediate to synthesize the side chain of cholesterol-lowering drug atorvastatin. To biosynthesize the (S)-CHBE, a recombinant Escherichia coli harboring the carbonyl reductase and glucose dehydrogenase was successfully constructed. The recombinant E. coli was cultured in a 500-L fermentor; after induction and expression, the enzyme activity and cell biomass were increased to 23,661.65 U/L and 13.90 g DCW/L which was 3.24 and 2.60-folds compared with those in the 50 L fermentor. The biocatalytic process for the synthesis of (S)-CHBE in an aqueous-organic solvent system was constructed and optimized with a substrate fed-batch strategy. The ethyl 4-chloro-3-oxobutanoate concentration reached to 1.7 M, and the (S)-CHBE with yield of 97.2 % and enantiomeric excess (e.e.) of 99 % was obtained after 4-h reaction in a 50-L reactor. In this study, the space-time yield and space-time yield per gram of biomass (dry cell weight, DCW) were 413.17 mM/h and 27.55 mM/h/g DCW for (S)-CHBE production, respectively, which were the highest values as compared to previous reports. Finally, (S)-CHBE was extracted from the reaction mixture with 82 % of yield and 95 % of purity. This study paved the foundation for the upscale production of (S)-CHBE by biocatalysis method.
Assuntos
Oxirredutases do Álcool/metabolismo , Butiratos/metabolismo , Escherichia coli/metabolismo , Glucose 1-Desidrogenase/metabolismo , Engenharia Metabólica , Solventes , Oxirredutases do Álcool/genética , Escherichia coli/genética , Escherichia coli/crescimento & desenvolvimento , Glucose 1-Desidrogenase/genética , Dados de Sequência Molecular , Proteínas Recombinantes/genética , Proteínas Recombinantes/metabolismo , Análise de Sequência de DNARESUMO
Methionine as an essential amino acid has been attracting more attention for its important applications in food and feed additives. In this study, for efficient production of methionine from 2-amino-4-methylthiobutanenitrile, a codon-optimized nitrilase gene was newly synthesized and expressed, and the catalytic conditions for methionine production were studied. The optimal temperature and pH for methionine synthesis were 40 °C and 7.5, respectively. The recombinant nitrilase was thermo-stable with half-life of 5.52 h at 40 °C. The substrate loading was optimized in given amount of catalyst and fixed substrate/catalyst ratio mode to achieve higher productivity. Methionine was produced in 100 % conversion within 120 min with a substrate loading of 300 mM. The production of methionine with the immobilized resting cells in packed-bed reactor was investigated. The immobilized nitrilase exhibited good operation stability and retained over 80 % of the initial activity after operating for 100 h. After separation, the purity and the total yield of methionine reached 99.1 and 97 %, respectively. This recombinant nitrilase could be a potential candidate for application in production of methionine.
Assuntos
Aminoidrolases/química , Proteínas de Bactérias/química , Escherichia coli/genética , Metionina/síntese química , Nitrilas/química , Aminoidrolases/genética , Aminoidrolases/isolamento & purificação , Proteínas de Bactérias/genética , Proteínas de Bactérias/isolamento & purificação , Biocatálise , Células Imobilizadas , Comamonadaceae/enzimologia , Estabilidade Enzimática , Meia-Vida , Concentração de Íons de Hidrogênio , Metais/química , Metionina/biossíntese , Nitrilas/metabolismoRESUMO
A gene encoding halohydrin dehalogenase (HHDH) from Agrobacterium tumefaciens CCTCC M 87071 was cloned and expressed in Escherichia coli. To increase activity and stability of HHDH, 14 amino acid residues around the active site and substrate-binding pocket based on the structural analysis and molecular docking were selected as targets for site-directed mutagenesis. The studies showed that the mutant HHDH (Mut-HHDH) enzyme had a more accessible substrate-binding pocket than the wild-type HHDH (Wt-HHDH). Molecular docking revealed that the distance between the substrate and active site was closer in mutant which improved the catalytic activity. The expressed Wt-HHDH and Mut-HHDH were purified and characterized using 1,3-dichloro-2-propanol (1,3-DCP) as substrates. The specific activity of the mutant was enhanced 26-fold and the value of k cat was 18.4-fold as compared to the Wt-HHDH, respectively. The Mut-HHDH showed threefold extension of half-life at 45 °C than that of Wt-HHDH. Therefore it is possible to add 1,3-DCP concentration up to 100 mM and epichlorohydrin (ECH) was produced at a relatively high conversion and yield (59.6 %) using Mut-HHDH as catalyst. This Mut-HHDH could be a potential candidate for the upscale production of ECH.
Assuntos
Agrobacterium tumefaciens/enzimologia , Epicloroidrina/metabolismo , Hidrolases/genética , Hidrolases/metabolismo , Agrobacterium tumefaciens/genética , Biocatálise , Biotransformação , Domínio Catalítico , Clonagem Molecular , Estabilidade Enzimática , Epicloroidrina/análise , Epicloroidrina/química , Escherichia coli/genética , Cromatografia Gasosa-Espectrometria de Massas , Meia-Vida , Concentração de Íons de Hidrogênio , Hidrolases/química , Metais/farmacologia , Modelos Moleculares , Simulação de Acoplamento Molecular , Mutagênese Sítio-Dirigida , Especificidade por Substrato , Temperatura , alfa-Cloridrina/análogos & derivados , alfa-Cloridrina/metabolismoRESUMO
A facile and efficient one-pot, single-step method for deracemizing a broad range of 2-hydroxyacids to (R)-2-hydroxyacids was established by combination of resting cells of an (S)-hydroxyacid dehydrogenase-producing microorganism and an (R)-ketoacid reductase-producing microorganism.
Assuntos
Oxirredutases do Álcool/metabolismo , Biocatálise , Hidroxiácidos/química , Oxirredução , Pseudomonas aeruginosa/enzimologia , Saccharomyces cerevisiae/enzimologia , Estereoisomerismo , Especificidade por SubstratoRESUMO
Pseudomonas aeruginosa ZJB1125 harboring a stereoselective 2-hydroxyacid dehydrogenase (2-HADH) can catalyze asymmetric oxidation of mandelic acid and 2-chloromandelic acid into (R)-isomers and corresponding 2-ketoacids with high activity and enantioselectivity, while no consecutive oxidation of 2-ketoacids was observed during whole-cell catalysis. The 2-HADH in P. aeruginosa ZJB1125 is a FMN-dependent flavoprotein and did not require NAD(P)⺠as cofactors to catalyze the oxidation reaction. Enzyme activity staining identified 2-HADH as the key enzyme that enantioselectively oxidized (S)-hydroxyacid to 2-ketoacid. The 2-HADH in P. aeruginosa ZJB1125 is inducible and 2-chloromandelic acid was found to induce its synthesis efficiently. The bacterium displayed pretty high activity and enantioselectivity for most of the aromatic 2-hydroxyacids examined, and have a potential for the concurrent obtaining of aromatic (R)-2-hydroxyacids and aromatic 2-ketoacids in near theoretical conversions. Using a simple organic extract process, aromatic (R)-2-hydroxyacids and aromatic 2-ketoacids can be effectively separated from the biocatalytic reaction mixture with high yield (>95%). This work provided a novel method for the concurrent obtaining of aromatic (R)-2-hydroxyacids and aromatic 2-ketoacids by oxidation of aromatic 2-hydroxyacids in one-step biotransformation, which would be a valuable process due to its high atom economy.
Assuntos
Cetoácidos/metabolismo , Ácidos Mandélicos/metabolismo , Pseudomonas aeruginosa/metabolismo , Oxirredutases do Álcool/metabolismo , Proteínas de Bactérias/metabolismo , Biomassa , Biotransformação , Fermentação , Concentração de Íons de Hidrogênio , Isomerismo , Cetoácidos/química , Ácidos Mandélicos/química , Oxirredução , Filogenia , Pseudomonas aeruginosa/classificação , Pseudomonas aeruginosa/enzimologia , TemperaturaRESUMO
In this study, several nitrilase genes from phylogenetically distinct organisms were expressed and purified in E. coli in order to study their ability to mediate the biotransformation of nitriles. We identified three nitrilases: Acidovorax facilis nitrilase (AcN); Alcaligenes fecalis nitrilase (AkN); and Rhodococcus rhodochrous nitrilase (RkN), which catalyzed iminodiacetonitrile (IDAN) to iminodiacetic acid (IDA). AcN demonstrated 8.8-fold higher activity for IDAN degradation as compared to AkN and RkN. Based on homology modeling and previously described 'hot spot' mutations, several AcN mutants were screened for improved activity. One mutant M3 (F168V/L201N/S192F) was identified, which demonstrates a 41% enhancement in the conversion as well as a 2.4-fold higher catalytic efficiency towards IDAN as compared to wild-type AcN.
Assuntos
Acetonitrilas/metabolismo , Aminoidrolases/metabolismo , Proteínas de Bactérias/metabolismo , Iminoácidos/metabolismo , Alcaligenes faecalis/enzimologia , Aminoidrolases/química , Aminoidrolases/genética , Aminoidrolases/isolamento & purificação , Proteínas de Bactérias/química , Proteínas de Bactérias/genética , Proteínas de Bactérias/isolamento & purificação , Biotransformação , Cromatografia Líquida de Alta Pressão , Dicroísmo Circular , Comamonadaceae/enzimologia , Escherichia coli , Hidrólise , Cinética , Simulação de Acoplamento Molecular , Mutação , Estrutura Secundária de Proteína , Proteínas Recombinantes/química , Proteínas Recombinantes/isolamento & purificação , Proteínas Recombinantes/metabolismo , Rhodococcus/enzimologia , Alinhamento de Sequência , Homologia de Sequência de AminoácidosRESUMO
A novel and simple methodology for co-obtaining of enantiomerically pure α-hydroxyacids and α-ketoacids was developed by enantioselective oxidation of α-hydroxyacids bearing a substituent with an aryl group using α-hydroxyacid dehydrogenase (α-HADH). A high-throughput method was firstly established for screening of enantioselective α-HADHs. Sinorhizobium sp. ZJB1 101 with high activity and excellent enantioselectivity of α-HADH for oxidation of α-hydroxyacids bearing a substituent with an aryl group was isolated and identified. This strain has potential for co-production of (R)-α-hydroxyacids and α-ketoacids in near theoretical yields, while no consecutive oxidation of α-ketoacids was observed. The green conversion system appears promising for potential applications in industry.
Assuntos
Oxirredutases do Álcool/metabolismo , Biotecnologia/métodos , Ensaios de Triagem em Larga Escala/métodos , Hidroxiácidos/isolamento & purificação , Cetoácidos/isolamento & purificação , Sinorhizobium/enzimologia , Oxirredutases do Álcool/química , Catálise , Hidroxiácidos/química , Hidroxiácidos/metabolismo , Cetoácidos/química , Cetoácidos/metabolismo , Estrutura Molecular , OxirreduçãoRESUMO
The D-threo form of p-methylsulfonylphenyl serine ethyl ester (MPSE) is a key intermediate for the synthesis of florfenicol. In this study, chiral resolution of DL-threo-p-MPSE with lipases was investigated. Among a series of lipases, Novzyme 435 was the best to resolve DL-threo-p-MPSE with the conversion rate of 36.83% and ee value of 35.13%. To improve the conversion rate and ee value, a number of byproducts were identified and characterized using reverse-phase HPLC, normal-phase HPLC, (1)H NMR, and LC-MS when threo-p-MPSE was hydrolyzed by lipases in organic medium. Mechanisms of generating main byproducts are proposed, and a suppressing method is provided. The results showed that byproduct p-methylsulfonyl benzaldehyde serves as the key intermediate during the whole side reaction process. It was also observed that threo-p-MPSE with a proper hydrolytic velocity served as a driving force to generate p-methylsulfonyl benzaldehyde and accelerated the side reactions. Finally, a feasible approach to suppress side reactions in enzymatic catalysis is offered. The conversion rate and ee value were greatly improved by 69.29 and 46.26%, respectively, using Zn(2+) compared to those without Zn(2+).
Assuntos
Lipase/química , Sulfonas/química , Cromatografia Líquida de Alta Pressão , Cromatografia Líquida , Ésteres , Concentração de Íons de Hidrogênio , Espectroscopia de Ressonância Magnética , Espectrometria de Massas , Estereoisomerismo , TemperaturaRESUMO
A codon-optimized 2-deoxyribose-5-phosphate aldolase (DERA) gene was newly synthesized and expressed in Escherichia coli to investigate its biochemical properties and applications in synthesis of statin intermediates. The expressed DERA was purified and characterized using 2-deoxyribose-5-phosphate as the substrate. The specific activity of recombinant DERA was 1.8 U/mg. The optimum pH and temperature for DERA activity were pH 7.0 and 35 °C, respectively. The recombinant DERA was stable at pH 4.0-7.0 and at temperatures below 50 °C. The enzyme activity was inhibited by 1 mM of Ni(2+), Ba(2+) and Fe(2+). The apparent K (m) and V (max) values of purified enzyme for 2-deoxyribose-5-phosphate were 0.038 mM and 2.9 µmol min(-1) mg(-1), for 2-deoxyribose were 0.033 mM and 2.59 µmol min(-1) mg(-1), respectively, which revealed that the enzyme had similar catalytic efficiency towards phosphorylated and non-phosphorylated substrates. To synthesize statin intermediates, the bioconversion process for production of (3R, 5S)-6-chloro-2,4,6-trideoxyhexose from chloroacetaldehyde and acetaldehyde by the recombinant DERA was developed and a conversion of 94.4 % was achieved. This recombinant DERA could be a potential candidate for application in production of (3R, 5S)-6-chloro-2,4,6-trideoxyhexose.
Assuntos
Aldeído Liases/metabolismo , Acetaldeído/análogos & derivados , Acetaldeído/metabolismo , Aldeído Liases/química , Aldeído Liases/genética , Sequência de Aminoácidos , Biocatálise , Escherichia coli/genética , Concentração de Íons de Hidrogênio , Dados de Sequência Molecular , TemperaturaRESUMO
To isolate enantioselective α-hydroxyacid dehydrogenases (α-HADHs), a high-throughput screening method was established. 2,4-Dinitrophenylhydrazine solution forms a red-brown complex with ketoacid produced during the α-HADH-mediated oxidation of α-hydroxyacid. The complex can be easily quantified by spectrophotometric measurement at 458 nm. The enantioselectivity of α-HADH in each strain can be measured with this colorimetric method using (R)- and (S)-α-hydroxyacid concurrently as substrates to evaluate the apparent enantioselectivity (E (app)). The E (app) closely matches the value of true enantioselectivity (E (true)) determined by HPLC analysis. With this method, a total of 34 stains harboring enantioselective α-HADHs were selected from 526 potential α-HADH-producing microorganisms. Pseudomonas aeruginosa displayed the highest (S)-enantioselective α-HADH activity. This strain appears promising for potential application in industry to produce (R)-α-hydroxyacids. The method described herein represents a useful tool for the high-throughput isolation of enantioselective α-HADHs.
Assuntos
Oxirredutases do Álcool , Proteínas de Bactérias , Fenil-Hidrazinas/química , Pseudomonas aeruginosa/enzimologia , Oxirredutases do Álcool/química , Oxirredutases do Álcool/isolamento & purificação , Proteínas de Bactérias/química , Proteínas de Bactérias/isolamento & purificação , Sinorhizobium/enzimologia , Especificidade por SubstratoRESUMO
Brefeldin A (BFA) is a macrolide lactone antibiotic, possessing antitumor, antiviral, antifungal activities. In this work, a separation strategy involving one-step macroporous resin adsorption chromatography combined with crystallization was established for BFA purification from Eupenicillium brefeldianum CCTCC M 208113 fermentation broth. Among six macroporous resin adsorbents tested, the non-polar resin HZ830 had the best adsorption and desorption performance. The static equilibrium adsorption data fitted well with the Freundlich equation, and the adsorption kinetic followed the pseudo-second order model. Through experimental optimization of column adsorption and desorption, BFA in purity of 90.4% (w/w), 92.1% (w/w) yield was obtained by a one-step macroporous resin adsorption chromatography, using a stepwise elution protocol. Furthermore, high purity (>99%, w/w) of BFA crystals were prepared from E. brefeldianum CCTCC M 208113 fermentation broth in an overall recovery of 67.0% (w/w), using a combination of adsorption chromatography packed with non-polar macroporous adsorbent HZ830 and crystallization in acetone.
Assuntos
Brefeldina A/isolamento & purificação , Cromatografia Líquida/métodos , Eupenicillium/metabolismo , Adsorção , Cromatografia Líquida/instrumentação , Meios de Cultivo Condicionados , Difusão , Etanol , Eupenicillium/química , Fermentação , Cinética , Reagentes de Laboratório/química , Modelos Lineares , ÁguaRESUMO
Improvement of dihydroxyacetone (DHA) production by mutagenesis of ion beam implantation and medium optimization using response-surface methodology (RSM) were investigated in this work. More than 1000 mutant strains were selected through a mutagenesis method using N(+) ions implantation with a dose of 60 × (2.6 × 10(13)) ions/cm(2) and energy of 10 keV. Several high-yield mutant strains were showed the potent application for DHA production and the genetically stable mutant strain G. oxydans ZJB09113 was selected for optimization of cultivation condition by RSM. The optimal medium for DHA fermentation is composed (in g/L) of yeast extract 4.88, CaCO(3) 2.00, and glycerol 52.86 mL/L (initial pH 4.89). The maximal DHA concentration of 40.0 g/L was achieved after 24 hr of shaken flask fermentation at 30°C with 150 rpm, and 196.3% increase in DHA production in comparison with unoptimized conditions.
Assuntos
Técnicas de Cultura Celular por Lotes/métodos , Reatores Biológicos/microbiologia , Di-Hidroxiacetona/biossíntese , Fermentação , Gluconobacter oxydans/metabolismo , Análise de Variância , Meios de Cultura/química , Meios de Cultura/metabolismo , Gluconobacter oxydans/genética , Gluconobacter oxydans/efeitos da radiação , Glicerol/química , Glicerol/metabolismo , Íons/química , Íons/metabolismo , Mutação/genética , Mutação/efeitos da radiação , Nitrogênio/química , Nitrogênio/metabolismoRESUMO
A novel enzymatic route for the synthesis of 2-amino-2,3-dimethylbutyramide (ADBA), important intermediate of highly potent and broad-spectrum imidazolinone herbicides, from 2-amino-2,3-dimethylbutyronitrile (ADBN) was developed. Strain Rhodococcus boritolerans CCTCC M 208108 harboring nitrile hydratase (NHase) towards ADBN was screened through a sophisticated colorimetric screening method and was found to be resistant to cyanide (5 mM). Resting cells of R. boritolerans CCTCC M 208108 also proved to be tolerant against high product concentration (40 g l(-1)) and alkaline pH (pH 9.3). A preparative scale process for continuous production of ADBA in both aqueous and biphasic systems was developed and some key parameters of the biocatalytic process were optimized. Inhibition of NHase by cyanide dissociated from ADBN was successfully overcome by temperature control (at 10°C). The product concentration, yield and catalyst productivity were further improved to 50 g l(-1), 91% and 6.3 g product/g catalyst using a 30/70 (v/v) n-hexane/water biphasic system. Furthermore, cells of R. boritolerans CCTCC M 208108 could be reused for at lease twice by stopping the continuous reaction before cyanide concentration rose to 2 mM, with the catalyst productivity increasing to 12.3 g product/g catalyst. These results demonstrated that enzymatic synthesis of ADBA using whole cells of R. boritolerans CCTCC M 208108 showed potential for industrial application.
Assuntos
Aminobutiratos/metabolismo , Cianetos/farmacologia , Herbicidas/metabolismo , Hidroliases/metabolismo , Rhodococcus/enzimologia , Aminobutiratos/química , Biocatálise , Herbicidas/química , Hexanos/química , Rhodococcus/efeitos dos fármacosRESUMO
Acarbose, a potent α-glucosidase inhibitor, is as an oral anti-diabetic drug for treatment of the type two, noninsulin-dependent diabetes. Actinoplanes utahensis ZJB-08196, an osmosis-resistant actinomycete, had a broad osmolality optimum between 309 mOsm kg(-1) and 719 mOsm kg(-1). Utilizing this unique feature, an fed-batch culture process under preferential osmolality was constructed through intermittently feeding broths with feed medium consisting of 14.0 g l(-1) maltose, 6.0 g l(-1) glucose and 9.0 g l(-1) soybean meal, at 48 h, 72 h, 96 h and 120 h. This intermittent fed-batch culture produced a peak acarbose titer of 4878 mg l(-1), increased by 15.9% over the batch culture.
Assuntos
Acarbose/metabolismo , Técnicas de Cultura Celular por Lotes/métodos , Fermentação/fisiologia , Micromonosporaceae/fisiologia , Biomassa , Meios de Cultura/farmacologia , Fermentação/efeitos dos fármacos , Glucose/farmacologia , Maltose/farmacologia , Micromonosporaceae/efeitos dos fármacos , Micromonosporaceae/crescimento & desenvolvimento , Concentração Osmolar , Glutamato de Sódio/farmacologia , Fatores de TempoRESUMO
Nitrilases are important industrial enzymes that convert nitriles directly into the corresponding carboxylic acids. In the current work, the fragment with a length of 1068 bp that encodes the A. faecalis ZJUTB10 nitrilase was obtained. Moreover, a catalytic triad was proposed and verified by site-directed mutagenesis, and the detailed mechanism of this nitrilase was clarified. The substrate specificity study demonstrated that the A. faecalis ZJUTB10 nitrilase belongs to the family of arylacetonitrilases. The optimum pH and temperature for the purified nitrilase was 7-8 and 40 °C, respectively. Mg(2+) stimulated hydrolytic activity, whereas Cu(2+), Co(2+), Ni(2+), Ag(+), and Hg(2+) showed a strong inhibitory effect. The K(m) and v(max) for mandelonitrile were 4.74 mM and 15.85 µmol min(-1) mg(-1) protein, respectively. After 30 min reaction using the nitrilase, mandelonitrile at the concentration of 20 mM was completely hydrolyzed and the enantiomeric excess against (R)-(-)-mandelic acid was >99%. Characteristics investigation indicates that this nitrilase is promising in catalysis applications.
Assuntos
Alcaligenes faecalis/enzimologia , Alcaligenes faecalis/genética , Aminoidrolases/química , Aminoidrolases/genética , Proteínas de Bactérias/química , Proteínas de Bactérias/genética , Clonagem Molecular , Alcaligenes faecalis/química , Sequência de Aminoácidos , Aminoidrolases/metabolismo , Proteínas de Bactérias/metabolismo , Catálise , Estabilidade Enzimática , Cinética , Dados de Sequência Molecular , Alinhamento de Sequência , Especificidade por SubstratoRESUMO
Iminodiacetic acid (IDA) has been widely used as an important intermediate in the fine chemical industry. In this study, a novel synthesis route of IDA from iminodiacetonitrile by whole microorganisms was investigated. A strain with the capability of producing nitrilase, ZJB-09133, was isolated and identified, and later named Alcaligenes faecalis ZJB-09133. In addition, the detailed biocatalysis of iminodiacetonitrile to produce IDA using ZJB-09133 was investigated. The results showed that the conversion reached 65.3% in Na(2)HPO(4)-NaH(2)PO(4) buffer of pH 8.0 under the following conditions: cells in the amount of 0.075-g DCW/L, 1.5% substrate, conversion time of 8 h, and a reaction temperature of 35°C. To the best of our knowledge, this is the first time that the production of IDA using a biocatalysis method has been reported.