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刺孢小克银汉霉9980生物酶法制备D苯丙氨酸

D-phenylalanine Production by Aminoacylase from Cunnighamella Echinulata 9980

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【作者】 郭丽芸刘毅贾晓娟李兆兰焦庆才

【Author】 Guo Liyun, Liu Yi, Jia Xiaojuan, Li Zhaolan, Jiao Qingcai (State Key Laboratory of Pharmaceutical Biotechnology, Nanjing University, Nanjing 210093)

【机构】 南京大学医药生物技术国家重点实验室南京大学医药生物技术国家重点实验室 南京210093南京210093

【摘要】 筛选到一株产氨基酰化酶的真菌刺孢小克银汉霉9980,直接利用其菌体细胞拆分N乙酰DL苯丙氨酸,最终制得D苯丙氨酸。最适反应条件为:0.2mol/LN乙酰DL苯丙氨酸(含Co2+5×10-4mol/L),0.04g/mL菌体,在pH值为7.0、50℃条件下反应24h,拆分率达90%以上。产物经JK008阳离子交换树脂分离。N乙酰D苯丙氨酸经6mol/LHCl加热回流4h脱乙酰得D苯丙氨酸。DPhe[α]20D=+34.4°(水溶)。

【Abstract】 An enzymatic method for the production of D-phenylalanine by aminoacylases from Cunnighamella echinulata 9980 was developed. The optimum conditions were as follows: 0.2 mol/L N-Ac-DL-phenylalanine(including Co 2+ 5×10 -4mol/L),0.04 g/mL mycelia, pH 7.0. After 24 h incubation at 50 ℃,the conversion rate against N-Ac-L-phenylalanine was higher than 90%. L-phenylalanine and N-Ac-D-phenylalanine were separated and purified on JK008 ion exchange resin. N-Ac-D-phenylalanine was hydrolyzed by 6 mol/L hydrochloric acid for 4 h, then D-phenylalanine crystal was obtained. D-Phe[α] 20D=+34.4°(H2O).

【基金】 国家技术创新基金资助项目(02CJ130116)
  • 【文献出处】 化工进展 ,Chemical Industry and Engineering Progress , 编辑部邮箱 ,2005年12期
  • 【分类号】TQ463.2;TQ246
  • 【被引频次】2
  • 【下载频次】127
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