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利用野生型和突变型地分枝杆菌全细胞腈水解酶合成香草酸

Synthesis of vanillic acid using whole cell nitrilase of wild and mutant Gordonia terrae.

作者信息

Bhalla Tek Chand, Kumari Nisha, Kumar Vijay, Kumar Virender

机构信息

Department of Biotechnology, Himachal Pradesh University, Summer Hill Shimla, Himachal Pradesh, 171005, India.

出版信息

Bioprocess Biosyst Eng. 2016 Jan;39(1):67-73. doi: 10.1007/s00449-015-1490-8. Epub 2015 Nov 12.

Abstract

The resting cells of Gordonia terrae mutant E9 having enhanced nitrilase activity were used for biotransformation of 4-hydroxy-3-methoxybenzonitrile into vanillic acid. The maximum conversion was observed in 0.1 M phosphate buffer (pH 8.0), using 60 mM substrate and 0.75 mgDCW resting cells in 1 mL reaction at 40 °C. Km of the whole cell nitrilase of wild and mutant strains of G. terrae for this substrate were 20 and 16.6 mM, and Vmax were 0.19 and 0.95 Umg(-1)(DCW), respectively. Fed batch reaction for transformation of 4-hydroxy-3-methoxybenzonitrile using whole cell nitrilase of wild G. terrae resulted in 2.36 g of vanillic acid in 5 h with a catalytic and volumetric productivity of 0.78 gg(-1)(DCW) h(-1) and 4.72 gL(-1)h(-1), respectively. The whole cell nitrilase of G. terrae mutant E9 resulted in higher catalytic and volumetric productivity, i.e., 1.68 gg(-1)DCW h(-1) and 10 gL(-1)h(-1). A total 5.04 g of vanillic acid with 99% purity were accumulated in 100 mL of reaction after 5 h.

摘要

采用腈水解酶活性增强的戈登氏菌突变体E9的静息细胞,将4-羟基-3-甲氧基苯甲腈生物转化为香草酸。在0.1M磷酸盐缓冲液(pH 8.0)中,于40℃下1mL反应体系中使用60mM底物和0.75mgDCW静息细胞时,观察到最大转化率。戈登氏菌野生型和突变株全细胞腈水解酶对该底物的Km分别为20和16.6mM,Vmax分别为0.19和0.95Umg(-1)(DCW)。使用戈登氏菌野生型全细胞腈水解酶对4-羟基-3-甲氧基苯甲腈进行补料分批反应,5小时内得到2.36g香草酸,催化产率和体积产率分别为0.78gg(-1)(DCW) h(-1)和4.72gL(-1)h(-1)。戈登氏菌突变体E9的全细胞腈水解酶具有更高的催化产率和体积产率,即1.68gg(-1)DCW h(-1)和10gL(-1)h(-1)。5小时后,100mL反应体系中累积了5.04g纯度为99%的香草酸。

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