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L-丙氨酸转化菌发酵条件的优化
引用本文:徐慧,崔颖,王珊珊,田延军,贺强之,韩延雷,刘建军,朱坤福,祝蕾,姜国政.L-丙氨酸转化菌发酵条件的优化[J].食品研究与开发,2021,42(7):177-182.
作者姓名:徐慧  崔颖  王珊珊  田延军  贺强之  韩延雷  刘建军  朱坤福  祝蕾  姜国政
作者单位:齐鲁工业大学(山东省科学院)山东省食品发酵工业研究设计院,山东济南250013;山东朱氏药业集团有限公司,山东菏泽274300;烟台恒源生物股份有限公司,山东烟台265709
基金项目:山东省重大科技创新工程项目(2019JZZY010341);山东省泰山产业领军人才建设项目(鲁政办字<2019>190 号);山东省中央引导地方科技发展资金项目(YDZX20203700003052)
摘    要:产L-天冬氨酸-β-脱羧酶(L-aspartate-β-decarboxylase,Asd)菌株以L-天冬氨酸(L-aspartic acid,L-Asp)为底物转化生产L-丙氨酸,通过单因素及正交设计试验对睾丸酮丛毛单胞菌HY-08D培养基组成及发酵条件进行优化。结果表明,最佳培养基组成:富马酸1.0%、L-Asp 1.0%、谷氨酸1.0%、玉米浆干粉0.6%、酵母粉0.8%、氯化钠0.7%、磷酸二氢钾0.15%、硫酸镁0.1%,pH 6.0。产酶菌株HY-08D转化用培养液采用三级扩培,一级接二级使用0.1%低接种量,二级接三级使用10%的接种量,最适通气量为10 L/min。优化后培养液中HY-08D菌体量和酶活较初始提高约1倍,培养周期缩短6 h~8 h。

关 键 词:L-丙氨酸  睾丸酮丛毛单胞菌  发酵条件  酶活  优化
收稿时间:2020/6/3 0:00:00

Fermentation Conditions Optimization of L-Alanine-producing Bacteria
XU Hui,CUI Ying,WANG Shan-shan,TIAN Yan-jun,HE Qiang-zhi,HAN Yan-lei,LIU Jian-jun,ZHU Kun-fu,ZHU Lei,JIANG Guo-zheng.Fermentation Conditions Optimization of L-Alanine-producing Bacteria[J].Food Research and Developent,2021,42(7):177-182.
Authors:XU Hui  CUI Ying  WANG Shan-shan  TIAN Yan-jun  HE Qiang-zhi  HAN Yan-lei  LIU Jian-jun  ZHU Kun-fu  ZHU Lei  JIANG Guo-zheng
Affiliation:(Shandong Food Ferment Industry Research&Design Institute,Qilu University of Technology(Shandong Academy of Sciences),Jinan 250013,Shandong,China;Shandong Zhushi Pharmaceutical Group Co.,Ltd.,Heze 274300,Shandong,China;Yantai Hengyuan Bioengineering Co.,Ltd.,Yantai 265709,Shandong,China)
Abstract:The L-aspartate-β-decarboxylase(Asd)-producing strain transforms L-alanine with L-aspartic acid(L-Asp)as substrate.The single factor and orthogonal experiments were employed to optimize the culture medium and fermentation conditions for Asd production by Comamonas testosteroni HY-08D.The optimal fermentation medium consisted of the following:fumaric acid 1.0%,L-Asp 1.0%,glutamic acid 1.0%,corn starch powder 0.6%,yeast extract 0.8%,NaCl 0.7%,KH2PO40.15%,MgSO40.1%,pH 6.0.The medium for the transformation of HY-08D strain was expanded in three-stage culture.A low inoculation amount of 0.1%was used from the first to the second stage.10%quantity of inoculation was used from the second to the third stage.The optimal ventilatory capacity was 10 L/min.The biomass and enzyme activity of HY-08D in optimized medium had doubled,and the culture period was shortened by 6 h-8 h compared with the initial state.
Keywords:L-alanine  Comamonas testosteroni  fermentation condition  enzyme activity  optimization
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