Bench scale synthesis of p -hydroxybenzoic acid using whole-cell nitrilase of Gordonia terrae mutant E9

作者: Vijay Kumar , Virender Kumar , Neerja Thakur , Tek Chand Bhalla

DOI: 10.1007/S00449-015-1367-X

关键词:

摘要: Mutants of Gordonia terrae were generated using chemical mutagens for better activity, stability and higher substrate/product tolerance its nitrilase enzyme. Mutant E9 showed two-time increase in activity tolerated p-hydroxybenzonitrile (p-HBN) up to 50 mM. Response surface methodology inducer mediation approach further enhanced the production enzyme 2.5-fold. The bench scale p-hydroxybenzoic acid (p-HBA) was carried out a fed-batch reaction (500-mL scale) whole-cell mutant 0.1 M potassium phosphate buffer (pH 8.0) at 40 °C. Total six feedings each an interval 45 min resulted accumulation 360 mM (21.6 g) p-HBA with purity 99 %. catalytic volumetric productivity bioprocess G. improved 1.8 g h−1 g DCW −1 43.2 g L−1, respectively, from 0.78 g h−1 g 28.8 g L−1 resting cells wild strain. K m V max purified 55 U mg−1 1.8 mM p-HBN turnover number 36 s−1 × 10−3.

参考文章(37)
W G Shanabruch, R P Rein, I Behlau, G C Walker, Mutagenesis, by Methylating and Ethylating Agents, in mutH, mutL, mutS, and uvrD Mutants of Salmonella Typhimurium LT2 Journal of Bacteriology. ,vol. 153, pp. 33- 44 ,(1983) , 10.1128/JB.153.1.33-44.1983
Nitya Nand Sharma, Monica Sharma, Tek Chand Bhalla, An improved nitrilase-mediated bioprocess for synthesis of nicotinic acid from 3-cyanopyridine with hyperinduced Nocardia globerula NHB-2 Journal of Industrial Microbiology & Biotechnology. ,vol. 38, pp. 1235- 1243 ,(2011) , 10.1007/S10295-010-0902-7
S. K. Bhatia, P. K. Mehta, R. K. Bhatia, T. C. Bhalla, An isobutyronitrile-induced bienzymatic system of Alcaligenes sp. MTCC 10674 and its application in the synthesis of α-hydroxyisobutyric acid. Bioprocess and Biosystems Engineering. ,vol. 36, pp. 613- 625 ,(2013) , 10.1007/S00449-012-0817-Y
Kefeng Ni, Hualei Wang, Li Zhao, Minjie Zhang, Siyuan Zhang, Yuhong Ren, Dongzhi Wei, Efficient production of (R)-(-)-mandelic acid in biphasic system by immobilized recombinant E. coli. Journal of Biotechnology. ,vol. 167, pp. 433- 440 ,(2013) , 10.1016/J.JBIOTEC.2013.07.024
Rebecca E Parales, Jayna L Ditty, Laboratory evolution of catabolic enzymes and pathways. Current Opinion in Biotechnology. ,vol. 16, pp. 315- 325 ,(2005) , 10.1016/J.COPBIO.2005.03.008
S. C. Rastogi, A. Schouten, N. de Kruijf, J. W. Weijland, Contents of methyl‐, ethyl‐, propyl‐, butyl‐ and benzylparaben in cosmetic products Contact Dermatitis. ,vol. 32, pp. 28- 30 ,(1995) , 10.1111/J.1600-0536.1995.TB00836.X
Kohtaro Kirimura, Hiroaki Gunji, Rumiko Wakayama, Takasumi Hattori, Yoshitaka Ishii, Enzymatic Kolbe–Schmitt reaction to form salicylic acid from phenol: Enzymatic characterization and gene identification of a novel enzyme, Trichosporon moniliiforme salicylic acid decarboxylase Biochemical and Biophysical Research Communications. ,vol. 394, pp. 279- 284 ,(2010) , 10.1016/J.BBRC.2010.02.154
Vijay Kumar, Tek Chand Bhalla, Transformation ofp-hydroxybenzonitrile top-hydroxybenzoic acid using nitrilase activity ofGordonia terrae Biocatalysis and Biotransformation. ,vol. 31, pp. 42- 48 ,(2013) , 10.3109/10242422.2012.757761
S. K. Bhatia, P. K. Mehta, R. K. Bhatia, T. C. Bhalla, Optimization of arylacetonitrilase production from Alcaligenes sp. MTCC 10675 and its application in mandelic acid synthesis. Applied Microbiology and Biotechnology. ,vol. 98, pp. 83- 94 ,(2014) , 10.1007/S00253-013-5288-9