Bhalla Tek Chand, Kumari Nisha, Kumar Vijay, Kumar Virender
Department of Biotechnology, Himachal Pradesh University, Summer Hill Shimla, Himachal Pradesh, 171005, India.
Bioprocess Biosyst Eng. 2016 Jan;39(1):67-73. doi: 10.1007/s00449-015-1490-8. Epub 2015 Nov 12.
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.
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。