期刊文献+

底物诱导和分批补料对巨大芽孢杆菌环氧化物水解酶生物合成的影响 被引量:2

Effect of Substrate Induction and Fed-batch Operation on Biosynthesis of Epoxide Hydrolase from Bacillus megaterium ECU1001
下载PDF
导出
摘要 从土壤中筛选得到的巨大芽孢杆菌 ( Bacillus megaterium) ECU1 0 0 1所产环氧化物水解酶能高度对映选择性地水解外消旋缩水甘油苯基醚。在摇瓶和 5L发酵罐中培养时初始产酶水平分别为 1 1 .0 U/L和 31 .0 U/L。通过添加底物诱导 ,可使摇瓶培养中酶量达到 61 .0 U/L;在 5L发酵罐中通过补料分批发酵 ,酶活可进一步提高到 96. An epoxide hydrolase biosynthesized by Bacillus megaterium EUC1001 isolated from soil can hydrolyze racemic phenyl glycidyl ether (PGE) with high enantioselectivity. Initial activities of the epoxide hydrolase obtained in flask and 5L fermentor were 11.0U/L and 31.0U/L, respectively. The enzyme activity in flask reached 61.0U/L by adding the substrate as an inducer and it could even reach 96.6U/L through fed batch fermentation in a 5L fermentor.
出处 《华东理工大学学报(自然科学版)》 CAS CSCD 北大核心 2001年第3期243-246,共4页 Journal of East China University of Science and Technology
基金 荷兰 DSM公司委托研究项目 !(ACER 980 8-0 12 6)
关键词 缩水甘油苯基醚 环氧化物水解酶 巨大芽孢杆菌 底物诱导 分批补料发酵 产酶水平 生物合成 phenyl glycidyl ether epoxide hydrolase Bacillus megaterium substrate induction fed batch fermentation
  • 相关文献

参考文献3

  • 1唐燕发 许建和 等.微生物环氧化物水解酶的研究与应用新进展[J].化学通报(网络版),2000,13:106-106.
  • 2Tang Y F,催化学报,2001年,22卷,1期,1页
  • 3唐燕发,化学通报.网络版,2000年,13卷,00106页

共引文献1

同被引文献16

  • 1TEJ BHATNAGAR,KELATH M M,JACQUES C,et al.A spectrophotometric method to assay e-poxide hydrolase activity[J].J Biochem Biop-hys Methods,2001,50(1):1-13.
  • 2KARBOUNE S,ARCHELAS A,FURSTOSS R,et al.Immobilization of epoxide hydrolase from Asperg-illus niger onto DEAE-cellulose:enzymatic pr-operties and application for the enantioselecti-ve resolution of a racemic epoxide[J].Molecular Catalysis B:Enzymatic,2005,32(5):175-183.
  • 3ROMANOV A O,SANDRA F M,WOLFGA K,et al.Chemoenzymatic deracemiza-tion of (±) -2,2-disubstituted oxiranes[J].Tetrahedron,1998,54(6):859-874.
  • 4Mahen M, Biedendiedk R, Gainer M ,et al.A Bacillus megaterium plasmid system for the production,export,and one-step purification of affinity-tagged heterologous levansucrase from growth medium [J].Appl Environ Microbiol, 2006,72(2) : 1677- 1679.
  • 5Malten M,Hollmann R,Dedkwer W D,et al.Production and secretion of recombinant Leuconostoc mesenteroides dextransucrase DsrS in Bacillus megaterium[J].Biotchnol Bioeng, 2005,89 : 206 - 218.
  • 6Rygus T,Hillen W.Inducible high-level expression of heterologous genes in Bacillus megaterium using the regulatory elements of the xylose-utilization operon[J].Appl Microbiol Biotechnol, 1991,35:594-599.
  • 7Vary P S.Prime time for Bacillus megaterium[J].Microbiology, 1994,140: 1001 - 1013.
  • 8Wang W,Hollmann R,Deckwer W D.Comparative proteomic analysis of high cell density- cultivations with two recombinant Bacillus megaterium strains for the production of a heterologous dextransucrase[J].Proteorne Science, 2006.4:19.
  • 9Wang W,Hollmann R, Furch T,et al.Proteomic analysis of a recombinant Bacillus megaterium strain during heterologous production of a glueosyltransferase[J].Protcome Sci, 2005,3 : 4.
  • 10Yang Y,Biedendieck R.,Wang W,et al.High yield recombinant penicillin G amidase production and export into the growth medium using Bacillus megateriunl[J].Microb Cell Fact, 2006,5 : 36.

引证文献2

二级引证文献4

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部