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Enzymatic Production of l-Citrulline by Pseudomonas putida

机译:恶臭假单胞菌酶法生产瓜氨酸

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To develop an efficient method for the production of l-citrulline, optimum conditions for the conversion of l-arginine to l-citrulline by microbial l-arginine deiminase and for production of the enzyme were studied. A number of micro-organisms were screened to test their ability to form and accumulate l-citrulline from l-arginine. Pseudomonas putida was selected as the best organism. With this organism, enzyme activity as high as 9.20 units per ml could be produced by a shaking culture at 30 C in a medium containing glucose, ammonium phosphate, l-arginine hydrochloride, yeast extract, peptone, and inorganic salts. Appropriate addition of a surface active agent to the reaction mixture was found to shorten the time required for the conversion. A large amount of l-arginine hydrochloride was converted stoichiometrically to l-citrulline in 62 hr at 37 C. Accumulated l-citrulline was readily isolated in pure form by ordinary procedures with ion-exchange resins. Yields of isolated l-citrulline of over 90.5% from l-arginine hydrochloride were easily attainable.
机译:为了开发生产1-瓜氨酸的有效方法,研究了通过微生物1-精氨酸脱亚氨酶将1-精氨酸转化为1-瓜氨酸的最佳条件以及该酶的生产的最佳条件。筛选了许多微生物以测试其从l-精氨酸形成和积累l-瓜氨酸的能力。恶臭假单胞菌被选为最佳生物。对于这种生物,通过在含有葡萄糖,磷酸铵,1-精氨酸盐酸盐,酵母提取物,蛋白ept和无机盐的培养基中于30°C摇动培养,可以产生每毫升高达9.20单位的酶活性。发现向反应混合物中适当添加表面活性剂可缩短转化所需的时间。在37℃下在62小时内将大量的1-精氨酸盐酸盐化学计量地转化为1-瓜氨酸。通过常规方法用离子交换树脂容易地以纯净形式分离出积累的1-瓜氨酸。从左旋精氨酸盐酸盐中分离出的左旋瓜氨酸的产率很容易达到90.5%。

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