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来自简单节杆菌的编码3-酮甾体-Δ1-脱氢酶的ksdD基因在枯草芽孢杆菌中的表达。

Expression of ksdD gene encoding 3-ketosteroid-Delta1-dehydrogenase from Arthrobacter simplex in Bacillus subtilis.

作者信息

Li Y, Lu F, Sun T, Du L

机构信息

Tianjin Key Lab of Industrial Microbiology, College of Biotechnology, Tianjin University of Science and Technology, Tianjin, P. R. China.

出版信息

Lett Appl Microbiol. 2007 May;44(5):563-8. doi: 10.1111/j.1472-765X.2007.02134.x.

Abstract

AIMS

To improve KSDH enzyme activity and the transformation level for androst-4-ene-3,17-dione.

METHODS AND RESULTS

3-ketosteroid-Delta(1)-dehydrogenase gene from Arthrobacter simplex was expressed in Bacillus subtilis under the control of P43 promoter. The molecular weight of expressed enzyme was about 55 kDa by SDS-PAGE analysis. The activities of intracellular and extracellular soluble enzymes examined by spectrophotometrical method were 110 +/- 0.5 mU mg(-1) and 15 +/- 0.6 mU mg(-1) of protein, respectively. The transformation rate of androst-4-ene-3,17-dione was 45.3% in the B. subtilis recombinant cells.

CONCLUSIONS

The enzyme activity of KSDH expressed in B. subtilis was improved about 30-fold compared with that of Arthrobacter simplex, and the transformation level of androst-4-ene-3,17-dione by the B. subtilis recombinant cells was improved about 10-fold.

SIGNIFICANCE AND IMPACT OF THE STUDY

The recombinant B. subtilis cells used for biotransformation of steroids provide a new method for production of steroid medicine. The time required for transformation of B. subtilis is much shorter than that of other bacteria, which means it will have wider usage in biopharmaceutical industry.

摘要

目的

提高KSDH酶活性以及雄甾-4-烯-3,17-二酮的转化水平。

方法与结果

简单节杆菌的3-酮甾体-Δ(1)-脱氢酶基因在P43启动子控制下于枯草芽孢杆菌中表达。通过SDS-PAGE分析,表达酶的分子量约为55 kDa。采用分光光度法检测的细胞内和细胞外可溶性酶的活性分别为每毫克蛋白质110±0.5 mU和15±0.6 mU。枯草芽孢杆菌重组细胞中雄甾-4-烯-3,17-二酮的转化率为45.3%。

结论

在枯草芽孢杆菌中表达的KSDH酶活性相较于简单节杆菌提高了约30倍,且枯草芽孢杆菌重组细胞对雄甾-4-烯-3,17-二酮的转化水平提高了约10倍。

研究的意义和影响

用于甾体生物转化的重组枯草芽孢杆菌细胞为甾体药物的生产提供了一种新方法。枯草芽孢杆菌转化所需时间比其他细菌短得多,这意味着它在生物制药行业将有更广泛的应用。

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