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费氏弧菌luxA缺失突变体的构建及其共生能力

Construction and symbiotic competence of a luxA-deletion mutant of Vibrio fischeri.

作者信息

Visick K G, Ruby E G

机构信息

Department of Biological Sciences University of Southern California, Los Angeles 90089-0371, USA.

出版信息

Gene. 1996 Oct 10;175(1-2):89-94. doi: 10.1016/0378-1119(96)00129-1.

Abstract

Bioluminescence by the squid Euprymna scolopes requires colonization of its light organ by the symbiotic luminous bacterium Vibrio fischeri. Investigation of the genetic determinants underlying bacterial symbiotic competence in this system has necessitated the continuing establishment and application of molecular genetic techniques in V. fischeri. We developed a procedure for the introduction of plasmid DNA into V. fischeri by electroporation, and isolated a mutant strain that overcame the apparent restriction barrier between V. fischeri and Escherichia coli. Using the technique of electroporation in combination with that of gene replacement, we constructed a non-luminous strain of V. fischeri (delta luxA::erm). In addition, we used the transducing phage rp-1 for the first time to transfer a chromosomal antibiotic resistance marker to another strain of V. fischeri. The luxA mutant was able to colonize E. scolopes as quickly and to the same extent as wild type. This result suggested that, at least during the initial stages of colonization, luminescence per se is not an essential factor for the symbiotic infection.

摘要

乌贼费氏弧菌的生物发光需要共生发光细菌费氏弧菌在其发光器官中定殖。对该系统中细菌共生能力的遗传决定因素进行研究,需要不断建立和应用费氏弧菌的分子遗传技术。我们开发了一种通过电穿孔将质粒DNA导入费氏弧菌的方法,并分离出了一个克服了费氏弧菌与大肠杆菌之间明显限制屏障的突变菌株。利用电穿孔技术与基因替换技术相结合,我们构建了一株不发光的费氏弧菌菌株(ΔluxA::erm)。此外,我们首次使用转导噬菌体rp-1将染色体抗生素抗性标记转移到另一株费氏弧菌中。luxA突变体能够像野生型一样快速且以相同程度定殖于费氏弧菌。这一结果表明,至少在定殖的初始阶段,发光本身并非共生感染的必要因素。

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