›› 2009, Vol. 11 ›› Issue (3): 81-87.

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Screening of High Nitrite Reductase Producing Strains and the Optimization of Fermentation

ZHENG Huai-zhong 1,2, CHEN Fa-he 1, LI Shu-yan 2, SUN Jun-she 2, LIU Ping 2   

  1. 1.College of Bio-engineering, Jimei University, Fujian Xiamen 361021|2.College of Food Science and Nutritional Engineering, China Agricultural University, Beijing 100083, China
  • Received:2009-03-10 Revised:2009-04-16 Online:2009-06-15 Published:2009-06-15

亚硝酸还原酶高产菌株的筛选及发酵条件优化

郑怀忠1,2,陈发河1,李淑燕2,孙君社2,刘萍2   

  1. 1.集美大学生物工程学院, 福建 厦门 361021|2.中国农业大学食品科学与营养工程学院, 北京 100083
  • 通讯作者: 刘萍,副教授,博士,主要从事食品生物技术、生物制药研究。Tel:010-62737131;E-mail:liuping@cau.edu.cn
  • 作者简介:郑怀忠,硕士研究生,研究方向为食品生物技术。
  • 基金资助:

    国家863计划项目(2008AA10Z306)资助。

Abstract:

The nitrite reductase production strain B.megaterium MPF-906 was treated with UV. The high nitrite reductase producing mutant Z85 was obtained and its nitrite reductase activity was 28.76 U/mL. The effects of compositions of culture medium and cultural conditions on nitrite reductase production were investigated. The optimal culture media are: glucose 1.5%, beef extract 0.2%, (NH4)2SO4 0.1%,  K2HPO4 0.135%, KH2PO4 0.07%, NaCl 0.1%, MgSO4·7H2O 0.04%, MnSO4·H2O 0.001%, CaCl2·2H2O 0.002%. The fermentation conditions are 30℃ for 20 h, 160 rpm, initial pH 6.5 and 4% of inoculation. Under this optimized conditions, the nitrite reductase activity reached 45.94 U/mL.

Key words: nitrite reductase, UV, fermentation, condition optimization

摘要:

通过紫外线对巨大芽孢杆菌MPF-906进行了诱变处理,提高了产酶能力,变异株Z85酶活达到28.76 U/mL。进一步对其发酵条件进行研究,优化了培养基和培养条件。优化的培养基为:葡萄糖1.5%,牛肉膏0.2%,硫酸铵0.1%,K2HPO4 0.135%,KH2PO4 0.07%,NaCl 0.1%;无机盐溶液10 mL/L(即MgSO4·7H2O 0.04%、MnSO4·H2O 0.001%、CaCl2·2H2O 0.002%)。发酵条件为:摇床转速160 rpm,接种量4%,初始pH 6.5,30 ℃发酵20 h。在此最优化条件下,亚硝酸还原酶的酶活达到45.94 U/mL。

关键词: 亚硝酸还原酶;紫外诱变;发酵;条件优化

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