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Enzymatic production of L-citrulline by hydrolysis of the guanidinium group of L-arginine with recombinant arginine deiminase

机译:通过重组精氨酸脱亚氨酶水解L-精氨酸的胍基酶促生产L-瓜氨酸

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摘要

In this study, a simple, efficient enzymatic production process for the environmentally friendly synthesis of L-citrulline from L-arginine was developed using arginine deiminase (ADI) from Lactococcus lactis. Following overexpression of L. lactis ADI in Escherichia. coli BL21 (DE3) and experimental evolution using error-prone PCR, mutant FMME106 was obtained with a K-m for L-arginine of 3.5 mM and a specific activity of 195.7 U/mg. This mutant exhibited a maximal conversion of 92.6% and achieved a final L-citrulline concentration of 176.9 g/L under optimal conditions (190 g/L L-arginine, 15 g/L whole-cell biocatalyst treated with 2% isopropanol for 30 min, 50 degrees C, pH 7.2, 8h). The average L-citrulline synthesis rate of 22.1 g/L/h is considerably higher than that reported for other similar biocatalytic approaches, therefore the process developed in the present work has great potential for large-scale production of L-citrulline. (C) 2015 Published by Elsevier B.V.
机译:在这项研究中,使用乳酸乳球菌的精氨酸脱亚氨酶(ADI)开发了一种简单,高效的酶法生产工艺,用于从L-精氨酸环保合成L-瓜氨酸。在乳酸乳球菌ADI在大肠杆菌中过表达后。大肠杆菌BL21(DE3)和使用容易出错的PCR进行的实验发展,获得突变型FMME106,其L-精氨酸的K-m为3.5 mM,比活性为195.7 U / mg。该突变体最大转化率为92.6%,在最佳条件下(190 g / L L-精氨酸,15 g / L全细胞生物催化剂用2%异丙醇处理30分钟)的最终L-瓜氨酸浓度为176.9 g / L ,50摄氏度,pH 7.2、8小时)。 L-瓜氨酸的平均合成速率为22.1 g / L / h,比其他类似的生物催化方法要高得多,因此,本工作开发的方法具有大规模生产L-瓜氨酸的巨大潜力。 (C)2015由Elsevier B.V.发布

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