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野生型气荚膜的形成至少需要嗜盐菌质粒pNRC100的gvp基因簇中的十个基因。

Wild-type gas vesicle formation requires at least ten genes in the gvp gene cluster of Halobacterium halobium plasmid pNRC100.

作者信息

DasSarma S, Arora P, Lin F, Molinari E, Yin L R

机构信息

Department of Microbiology, University of Massachusetts, Amherst 01003.

出版信息

J Bacteriol. 1994 Dec;176(24):7646-52. doi: 10.1128/jb.176.24.7646-7652.1994.

Abstract

To study the functions of the 13 gvp genes, gvpMLKJIHGFEDACN, on plasmid pNRC100 of Halobacterium halobium in gas vesicle formation, we carried out linker scanning mutagenesis of the gene cluster. We constructed a 24.5-kb Escherichia coli-H. halobium shuttle plasmid, pFL2, containing the gvp gene cluster and introduced a kanamycin resistance (kappa) cassette into each gene (except for gvpA). Transformation of H. halobium SD109, which had the entire gvp gene cluster deleted, with pFL2 and mutated pFL2 derivatives showed that while the unmutated gene cluster successfully programmed gas vesicle formation, derivatives with insertion of the kappa cassette in any of the gvp genes, except gvpM, did not lead to production of normal gas vesicles. Insertions in gvpL, -K, -J, -I, and -F resulted in a complete block in gas vesicle synthesis, while insertions in gvpH, -G, -E, -D, -C, and -N resulted in greatly reduced gas vesicle synthesis. In most cases, the block in gas vesicle synthesis did not result from polar effects, since similar results were obtained for derivatives of the insertion mutants in which most of the internal portion of the kappa cassette was deleted and only small (15 to 54-bp) insertions remained. The only exceptions were for gvpH and gvpD, where deletion of the internal portion of the kappa insertions resulted in phenotypic reversion. Electron microscopic analysis of the kappa mutants revealed that interruptions of gvpC and gvpN result in the formation of smaller gas vesicle than in the wild type, while interruptions of gvpF, -G, -H, -J, -K, and -L produce no discernible vesicle intermediates. These results indicate the gvpA, -C, and -N, which have the rightward transcriptional orientation, encode structural proteins, with gvpC and gvpN necessary for late stages of vesicle formation, and gvpL, -K, -J, -I, -H, -G, and -F, which have the leftward transcriptional orientation encode proteins involved in early steps in the assembly of gas vesicles.

摘要

为了研究嗜盐嗜盐菌(Halobacterium halobium)质粒pNRC100上的13个gvp基因(gvpMLKJIHGFEDACN)在气泡形成中的功能,我们对该基因簇进行了接头扫描诱变。我们构建了一个24.5 kb的大肠杆菌-嗜盐嗜盐菌穿梭质粒pFL2,它包含gvp基因簇,并将卡那霉素抗性(kappa)盒导入每个基因(gvpA除外)。用pFL2和突变的pFL2衍生物转化缺失整个gvp基因簇的嗜盐嗜盐菌SD109,结果表明,未突变的基因簇成功地指导了气泡的形成,而在除gvpM外的任何gvp基因中插入kappa盒的衍生物均未导致正常气泡的产生。在gvpL、-K、-J、-I和-F中插入导致气泡合成完全受阻,而在gvpH、-G、-E、-D、-C和-N中插入导致气泡合成大大减少。在大多数情况下,气泡合成的阻断并非由极性效应引起,因为对于插入突变体的衍生物也得到了类似的结果,其中kappa盒的大部分内部被删除,仅留下小的(15至54 bp)插入片段。唯一的例外是gvpH和gvpD,其中kappa插入片段内部的缺失导致表型回复。对kappa突变体的电子显微镜分析表明,gvpC和gvpN的中断导致形成比野生型更小的气泡,而gvpF、-G、-H、-J、-K和-L的中断则不产生可识别的囊泡中间体。这些结果表明,具有向右转录方向的gvpA、-C和-N编码结构蛋白,其中gvpC和gvpN是气泡形成后期所必需的,而具有向左转录方向的gvpL、-K、-J、-I、-H、-G和-F编码参与气泡组装早期步骤的蛋白质。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/122e/197222/41c6347260e9/jbacter00042-0251-a.jpg

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