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首页> 外文期刊>Applied and Environmental Microbiology >The plasmid-encoded lactococcal envelope-associated proteinase is encoded by a chromosomal gene in Lactococcus lactis subsp. cremoris BC101.
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The plasmid-encoded lactococcal envelope-associated proteinase is encoded by a chromosomal gene in Lactococcus lactis subsp. cremoris BC101.

机译:质粒编码的乳球菌包膜相关蛋白酶由乳酸乳球菌亚种中的染色体基因编码。 cremoris BC101。

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The plasmid-free strain Lactococcus lactis subsp. cremoris BC101 produced an extracellular proteinase physicochemically similar to the proteinase encoded by the plasmid-linked prtP gene of other lactococcal strains. The absence of detectable plasmids in strain BC101 indicated that the prtP proteinase gene may be chromosomally located. The chromosomal linkage of the prtP proteinase gene in BC101 was confirmed by pulsed-field electrophoresis of chromosomal DNA and hybridization, using as a probe the plasmid-linked prtP gene from L. lactis subsp. cremoris Wg2. The prtM gene necessary for the maturation of the proteinase was also chromosomally located adjacent to prtP in BC101. By using as a hybridization probe the ISS1-like element ISS1W, which is found adjacent to the proteinase genes in both pWV05 and pSK111, specific homology to the chromosomal fragment containing the proteinase gene was found. DNA sequencing of a polymerase chain reaction product of chromosomal DNA upstream from prtM revealed a 123-nucleotide sequence which was 100% identical to the equivalent sequence in the ISS1W-containing plasmid. The terminal inverted repeat (18 nucleotides) of the ISS1W element was found in this sequenced DNA. These findings suggest that the chromosomal proteinase gene is organized in a fashion similar to that of the plasmid-linked proteinase gene.
机译:无质粒的乳酸乳球菌亚种。 creemoris BC101产生的细胞外蛋白酶在物理化学上类似于其他乳球菌菌株的质粒连接的prtP基因编码的蛋白酶。菌株BC101中没有可检测的质粒,表明prtP蛋白酶基因可能位于染色体上。 BC101中prtP蛋白酶基因的染色体连锁通过染色体DNA的脉冲场电泳和杂交来证实,使用来自乳杆菌亚种的质粒连接的prtP基因作为探针。 cremoris Wg2。蛋白酶成熟所需的prtM基因也位于染色体上,与BC101中的prtP相邻。通过使用与pWV05和pSK111中的蛋白酶基因相邻的ISS1样元件ISS1W作为杂交探针,发现与包含该蛋白酶基因的染色体片段具有特定的同源性。 prtM上游的染色体DNA的聚合酶链反应产物的DNA测序揭示了123个核苷酸的序列,该序列与含ISS1W的质粒中的等效序列100%相同。在该测序的DNA中发现了ISS1W元件的末端反向重复序列(18个核苷酸)。这些发现表明染色体蛋白酶基因的组织方式与质粒连接的蛋白酶基因的相似。

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