Kakimoto T, Shibatani T, Nishimura N, Chibata I
Appl Microbiol. 1971 Dec;22(6):992-9. doi: 10.1128/am.22.6.992-999.1971.
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.
为开发一种高效生产L-瓜氨酸的方法,研究了微生物L-精氨酸脱亚氨酶将L-精氨酸转化为L-瓜氨酸的最佳条件以及该酶的生产条件。筛选了多种微生物以测试它们从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菌株。用该菌株,在含有葡萄糖、磷酸铵、L-精氨酸盐酸盐、酵母提取物、蛋白胨和无机盐的培养基中于30℃振荡培养,可产生高达9.20单位/毫升的酶活性。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。大量的L-精氨酸盐酸盐在37℃下62小时内按化学计量转化为L-瓜氨酸。通过使用离子交换树脂的常规方法可轻松分离出纯形式的积累的L-瓜氨酸。从L-精氨酸盐酸盐中分离出的L-瓜氨酸产率很容易达到90.5%以上。