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以甘油为碳源分批补料高密度发酵产环氧化物水解酶 被引量:4

Glycerol as a Carbon Source to Produce Epoxide Hydrolase by High Cell Density Fed-Batch Cultivation
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摘要 环氧化物水解酶能够立体选择性地催化环氧化合物生成相应的二醇,具有重要的工业应用价值。通过摇瓶实验研究了不同甘油浓度对重组大肠杆菌Rosetta(DE3)/pET28(a)-CESH生长的影响,确定了IPTG最佳诱导时机、诱导浓度和诱导后培养温度。在15 L发酵罐进行放大培养,对比分批补料和批次发酵,前者生产率达6.71×105 U·(L·h)-1,比批次发酵提高了33.3%,酶活达到2.0×107 U·L-1,所用的时间,比批次发酵缩短了10 h,适合于工业应用。 Epoxide hydrolase is an important industrial enzyme which can stereo-selectively transform racemic epoxide into enantiomeric vicinal diol. In this study, the growth of E. coli Rosetta (DE3)/pET28(a)-CESH on different concentrations of glycerol was studied in shaking flask. Induction time, IPTG concentration and culture temperature after induction were optimized to enhance the production of CESH. The results reveal that in a 15 L fermentor, the fed-batch fermentation process can reduce the fermentation time by 10 hours. Compared with the batch fermentation process, the CESH productivity was increased by 33.3%during the whole process. These results indicate that the new process is suitable for industry application.
出处 《高校化学工程学报》 EI CAS CSCD 北大核心 2014年第3期600-605,共6页 Journal of Chemical Engineering of Chinese Universities
基金 国家科技部863项目(2014AA022105)
关键词 重组大肠杆菌 环氧化物水解酶 高密度发酵 甘油抑制 recombinant E. coli epoxide hydrolase high cell density cultivation glycerol inhibition
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  • 1郑志永,姚善泾.应用溶氧反馈控制高密度培养重组大肠杆菌过程中乙酸的产生[J].高校化学工程学报,2006,20(2):233-238. 被引量:19
  • 2胡沛臻,温江田,路凡,王孝功,李侠,司少艳,葛伟,黄杨,张秀敏,隋延仿.溶氧反馈-补料分批技术高密度培养基因重组MAGE1/HSP70/MAGE3工程菌[J].第三军医大学学报,2007,29(16):1576-1579. 被引量:7
  • 3张晓云,张艳军,李志敏,叶勤.大肠杆菌DH5α及其耐乙酸突变株DA19在氮源限制下的代谢和关键酶特性研究[J].生物工程学报,2007,23(5):896-901. 被引量:6
  • 4NIE Y,YAN W,XU Y,et al.High-level expression of bacillus naganoensis pullulanase from recombinant Escherichia coli with auto-induction:Effect of lac operator[J].PLo S ONE,2013,8(10):1-3.
  • 5YU S J,WANG Y X,LIU Y S,et al.Expression and purification of APRIL by auto-induction[J].Protein Expression and Purification,2009,68(1):49-53.
  • 6Gombert A K,Kilikian B V.Recombinant gene expression in Escherichia coli cultivation using lactose as inducer[J].Biotechnol,1998,60(1/2):47-54.
  • 7Studier F W.Protein production by auto-induction in highdensity shaking cultures[J].Protein Expression and Purification,2005,41(1):207-234.
  • 8KANG J,Park K M,Choi K H,et al.Molecular cloning and biochemical characterization of a heat-stable type I pullulanase from Thermotoga neapolitana[J].Enzyme and Microbial Technology,2010,48(3):260-266.
  • 9Mey M D,Maesneire S D,Wim S,et a1.Minimizing acetate formation in E.coli fermentations[J].Industrial Microbiology Biotechnology,2007,34(11):689-700.
  • 10Yano T,Endo T,Tuji T,et al.Fed-batch culture with a modified DO-stat method[J].Journal of Fermentation and Bioengineering,1991,71(1):35-38.

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