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rpoE基因对环境胁迫下肠炎沙门氏菌生长能力的影响 被引量:1

Influence of rpoE Gene on Growth Ability of Salmonella enteritidis under the Stress of Circumstance
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摘要 rpoE基因是普遍存在于细菌中的一类调节基因,对细菌响应各种环境胁迫起着重要的调节作用。该研究利用λ噬菌体的Red重组系统构建出肠炎沙门氏菌(Salmonella enteritidis,S.E)的rpoE基因缺陷株ΔrpoE,并考察ΔrpoE在不同环境胁迫条件下的生长能力。结果显示,在37°C时,ΔrpoE的生长能力无显著变化;而在高低温、酸、氧、高渗培养条件下,ΔrpoE的生长能力显著弱于野生株。该研究首次获得了S.E的基因缺陷株ΔrpoE,并初步探索了rpoE基因在S.E中的功能,有助于进一步研究rpoE基因在大肠杆菌、沙门氏菌等肠杆科细菌在响应环境胁迫过程中表现出的生物学功能。 rpoE gene is one kind of regulatory genes which can be commonly found in bacteria and plays an important role to various environmental stress response. In this study, an rpoE gene mutant of Salmonel- la enteritidis (S.E) called ArpoE was constructed by Z-Red recombinase system and the growth ability of △rpoE under different stress of circumstance was inspected. The results showed that there was no difference between wild and mutant strains at 37℃. However, the growth ability of mutant strains was significantly weaker than wild strains under the culture condition of high and low temperature, acidic, oxidative, high-osmotic. In sum- mary, this is the first time to get the rpoE knock-out mutant in Salmonella enteritidis and the function of rpoE gene is preliminarily inspected, which can help to find out the further function and mechanism of the rpoE gene in Enterobacteriaceae such as E.coli and S.E.
出处 《中国细胞生物学学报》 CAS CSCD 北大核心 2013年第5期583-588,共6页 Chinese Journal of Cell Biology
基金 国家自然科学基金(批准号:31071556 30871739) 国家高技术研究发展计划(批准号:2011AA100801)资助的课题~~
关键词 肠炎沙门氏菌 RED重组 ΔrpoE 环境胁迫 Salmonella enteritidis Red recombination ArpoE environment stress
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  • 1杨保伟,张秀丽,曲东,席美丽,崔生辉,申进玲,赵彪,寄宝义,孟江洪.2007-2008陕西部分零售畜禽肉沙门氏菌血清型和基因型[J].微生物学报,2010,50(5):654-660. 被引量:63
  • 2Kazmierczak M J, Wiedmann M, Boor KJ. Alternative sigma factors and their roles in bacterial virulence. Microbiol Mol Biol Rev 2005, 69(4): 527-43.
  • 3Kanehara K, Ito K, Akiyama Y. YaeL proteolysis of RseA is controlled by the PDZ domain of YaeL and a Gin-rich region of RseA. EMBO J 2003, 22(23): 6389-98.
  • 4李樊,刘义,何钢.基因敲除技术研究进展[J].生物技术通报,2008,24(2):80-82. 被引量:14
  • 5张雪,温廷益.Red重组系统用于大肠杆菌基因修饰研究进展[J].中国生物工程杂志,2008,28(12):89-93. 被引量:38
  • 6Datsenko KA, Wanner BL. One-step inactivation of chromosom- al genes in Escherichia coli K-12 using PCR products. Proc Natl Acad Sci USA 2000, 97(12): 6640-5.
  • 7Yu D, Ellis HM, Lee EC. An efficient recombination system for chromosome engineering in Eseheriehia eoli. Proc Natl Acad Sci USA 2000, 97(11): 5978-83.
  • 8Murphy KC. Use of bacteriophage recombination functions to promote gene replacement in Escherichia coil J Bacteriol 1998, 180: 2063-71.
  • 9Serra-Moreno R, Aeosta S, Hemalsteens JP. Use of the lambda Red recombinase system to produce recombinant prophages car- rying antibiotic resistance genes. BMC Mol Bio12006, 7:31.
  • 10Poteete AR. What makes the bacteriophage lambda Red system useful for genetic engineering: Molecular mechanism and bio- logical function. FEMS Micro-biol Lett 2001 , 201 (1): 9-14.

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