期刊文献+

龟裂链霉菌工业菌中zwf1基因的阻断对土霉素生物合成影响 被引量:3

Disruption of zwf1 gene encoding glucose-6-phosphate gehydrogenase enhances oxytetracycline biosynthesis in industrial Streptomyces rimosus
在线阅读 下载PDF
导出
摘要 目的运用代谢工程手段对龟裂链霉菌工业菌(Industrial Streptomyces rimosus,SRI)进行基因改造,提高土霉素(oxytetracycline,OTC)产量。方法利用pKC1139质粒阻断SRI基因组中葡萄糖-6-磷酸脱氢酶(glucose-6-phosphate dehydrogenase)编码基因zwf1。结果筛选得到一株OTC高产突变株,将突变株与原始菌株进行发酵,发现OTC产量比原始菌株提高了36.2%。结论 SRI基因组中zwf1基因的缺失使细胞合成土霉素的能力增强;龟裂链霉菌中初级代谢关键基因调控会影响次级代谢。 Objective To enhance oxytetracyclin (OTC) production in Industrial Streptomyces rimosus by gene disruption according to metabolic engineering principle. Methods Disrupt zwfl gene encoding glucose-6-phosphate dehydrogenase in SRI strain using plasmid pKCl139. Results A mutant strain was successfully constructed and screened which produced OTC 36.2% more than parent strain. Conclusion The results suggest that it is an effective way to enhance OTC productivity in an industrial strain by zwfl knock-out. The regulation of key genes in primary metabolic affects secondary metabolic in S. rirnosus a lot.
出处 《中国抗生素杂志》 CAS CSCD 北大核心 2012年第1期35-38,69,共5页 Chinese Journal of Antibiotics
基金 生物反应器国家重点实验室开放课题(2060204) 国家支撑项目<抗生素大规模生产关键技术创新-抗生素发酵工艺与装备集成创新研究>(2007BAI26B02)
关键词 龟裂链霉菌工业菌 葡萄糖-6-磷酸脱氢酶 基因阻断 土霉素生物合成 Industrial Streptomyces rimosus Glucose-6-phosphate dehydrogenase Gene disruption Oxytetracycline biosynthesis
  • 相关文献

参考文献1

二级参考文献1

共引文献8

同被引文献79

  • 1侯进,沈煜,鲍晓明.酿酒酵母木糖代谢工程中辅酶工程的研究进展[J].中国生物工程杂志,2006,26(2):89-94. 被引量:11
  • 2Baltz RH. Renaissance in antibacterial discovery from actinomycetes[J]. Current Opinion in Phar- macology, 2008, 8(5): 557-563.
  • 3Olano C, Mendez C, Salas JA. Antitumor com- pounds from actinomycetes: from gene clusters to new derivatives by combinatorial biosynthesis[J]. Natural Product Reports, 2009, 26(5): 628-660.
  • 4Jarboe LR, Zhang X, Wang X, et al. Metabolic en- gineering for production of biorenewable fuels and chemicals: contributions of synthetic biology[J]. Journal of Biomedicine and Biotechnology, 2010, 761042: 1-18.
  • 5Park JH, Lee SY, Kim TY, et al. Application of systems biology for bioprocess development[J]. Trends in Biotechnology, 2008, 26(8): 404-412.
  • 6Mainguet SE, Liao JC. Bioengineering of microor- ganismsfor C3 to C5 alcohols production[J]. Bio- technology Journal, 2010, 5(12): 1297-1308.
  • 7Blazeck J, Alper H. Systems metabolic engineering: genome-scale models and beyond[J]. Biotechnol- ogy Journal, 2010, 5(7): 647-659.
  • 8Zhang SL, Ye BC, Chu J, et al. From multi-scale methodology to systems biology: to integrate strain improvement and fermentation optimization[J]. Journal of Chemical Technology and Biotechnol- ogy, 2006, 81: 734-745.
  • 9Stutzman-Engwall K, Conlon S, Fedechko R, et al. Semi-synthetic DNA shuffling of aveC leads to improved industrial scale production of doramectin by Streptomyces avermitilis[J]. Metabolic Engi- neering, 2005, 7(1): 27-37.
  • 10Stephanopoulos G. Metabolic engineering by ge- nome shuffling[J]. Nature Biotechnology, 2002, 20: 666-668.

引证文献3

二级引证文献3

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