畜牧与饲料科学 ›› 2013, Vol. 34 ›› Issue (9): 32-32.doi: 10.12160/j.issn.1672-5190.2013.09.012

• 基础科学 • 上一篇    下一篇

高产淀粉酶枯草芽胞杆菌的诱变选育和酶学性质研究

恒子钤[1,2] 丁轲[1,2,3] 彭春平[1,2] 罗伟光[1,2] 李三栋[2] 张小明[2] 任雪[2] 余祖华[1]   

  1. [1]河南省动物疫病与公共安全院士工作站,河南洛阳471003 [2]河南科技大学宏翔发酵饲料实验室,河南洛阳471003 [3]河南省高等学校环境与畜产品安全重点学科开放实验室,河南洛阳471003
  • 出版日期:2013-09-20 发布日期:2013-09-20
  • 通讯作者: 恒子钤
  • 作者简介:作者简介:恒子钤(1991-),女,主要研究方向为动植物检疫。 通讯作者:丁轲(1977-),男,副教授,博士,硕士生导师,主要研究方向为动物微生态学。
  • 基金资助:
    基金项目:河南省教育厅重点项目(138230978);河南科技大学SRTP项目(20122244).

Study on the Mutation Breeding and Enzymatic Characteristics of Highly Produced Amylase Bacillus subtilis

HENG Zi-qin,DING Ke,PENG Chun-ping, LUO Wei-guang,LI San-dong,ZHANG Xiao-ming, REN Xue,YU Zu-hua (1.Animal Disease and Public Safety Academician Workstation of Henan Province, Luoyang 471003, China;2.Femlented Feed Laboratory of Hongxiang, Henan University of Science and Technology, Luoyang 471003, China ; 3.Key Course Open Laboratory of Environment and Animal Products Safe of Henan Province Supreme Institution, Luoyang 471003, China )   

  • Online:2013-09-20 Published:2013-09-20

摘要: 为了提高产淀粉酶枯草芽胞杆菌BacillussubtilisN21的酶活,试验采用紫外线对该菌株进行诱变,并对该淀粉酶的部分酶学性质进行了研究。结果表明,淀粉酶酶活由出发株的32.96U/mL增加到86.24U/mL.比原菌株酶活提高了161.65%。该酶的最适反应温度为35℃,最适pH值为7.0,在30—40℃,pH值为5.0~8.0条件下较稳定。Ca2+和Mn2+对酶有激活作用,Cu2+、Zn2+对酶有抑制作用,而Mg2+、Fe2+对其影响较小。说明筛选出1株产酶活性较强的突变菌株。

Abstract: In order to improve the enzyme activity of produced amylase Bacillus subtilis N21, this strain was mutated with UV. And some characteristics of amylase were studied. The results showed that the amylase activity of mutant increased from 32.96 U/ mL to 86.24 U/mL, which increased by 161.65% than that of the original strain. The optimal reaction temperature was 35 ℃, the optimal pH value was 7.0. And The amylase activity was stable under the conditions of 30-40℃, pH of 5.0-8.0. Ca2+and Mn2+ could activate amylase, and Cu2+ and Zn2+ could inhibit amylase activity. And Mg2+ and Fe2+ had smaller effects on amylase activity. It was indicated that a mutant strain with higher activity of high-produced amylase was screened out.

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