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Replication and temperature-sensitive maintenance functions of lactose plasmid pSK11L from Lactococcus lactis subsp. cremoris.

机译:乳酸乳球菌亚种的乳糖质粒pSK11L的复制和温度敏感性维持功能。 creemoris。

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摘要

The replication region of pSK11L, the lactose plasmid of Lactococcus lactis subsp. cremoris (L. cremoris) SK11, was isolated on a 14.8-kbp PvuII fragment by shotgun cloning into an Escherichia coli vector encoding erythromycin resistance and selection for erythromycin-resistant transformants of L. lactis subsp. lactis (L. lactis) LM0230. Deletion analysis and Tn5 mutagenesis of the resulting plasmid (pKMP1) further localized the replication region to a 2.3-kbp ScaI-SpeI fragment. DNA sequence analysis of this 2.3-kbp fragment revealed a 1,155-bp open reading frame encoding the putative replication protein, Rep. The replication origin was located upstream of rep and consisted of an 11-bp imperfect direct repeat and a 22-bp sequence tandemly repeated three and one-half times. The overall organization of the pSK11L replicon was remarkably similar to that of pCI305, suggesting that pSK11L does not replicate by the rolling-circle mechanism. Like pSK11L, pKMP1 was unstable in L. lactis LM0230. Deletion analysis allowed identification of several regions which appeared to contribute to the maintenance of pKMP1 in L. lactis LM0230. pKMP1 was significantly more stable in L. cremoris EB5 than in L. lactis LM0230 at all of the temperatures compared. This stability was lost by deletion of a 3.1-kbp PvuII-XbaI fragment which had no effect on stability in L. lactis LM0230. Other regions affecting stability in L. cremoris EB5 but not in L. lactis LM0230 were also identified. Stability assays conducted at various temperatures showed that pKMP1 maintenance was temperature sensitive in both L. lactis LM0230 and L. cremoris EB5, although the plasmid was more unstable in L. lactis LM0230. The region responsible for the temperature sensitivity phenotype in L. lactis LM0230 was tentatively localized to a 1.2-kbp ClaI-HindIII fragment which was distinct from the replication region of pSK11L. Our results suggest that the closely related L. lactis and L. cremoris subspecies behave differently regarding maintenance of plasmids.
机译:乳酸乳球菌亚种的乳糖质粒pSK11L的复制区。通过将shot弹枪克隆到编码红霉素抗性的大肠杆菌载体中,并选择乳酸乳杆菌亚种的红霉素抗性转化子,在14.8kbp PvuII片段上分离出了cremoris(Cremoris)SK11。乳酸(乳酸乳球菌)LM0230。所得质粒(pKMP1)的缺失分析和Tn5诱变进一步将复制区域定位在2.3-kbp ScaI-SpeI片段上。对该2.3kbp片段的DNA序列分析显示了一个1,155bp的开放阅读框,编码假定的复制蛋白Rep。复制起点位于rep的上游,由一个11bp的不完全直接重复序列和一个22bp的串联序列组成。重复三遍半。 pSK11L复制子的整体结构与pCI305非常相似,这表明pSK11L不能通过滚环机制复制。像pSK11L一样,pKMP1在乳酸乳球菌LM0230中不稳定。缺失分析允许鉴定似乎有助于乳酸乳球菌LM0230中pKMP1维持的几个区域。在所有比较温度下,克雷莫氏菌EB5中的pKMP1均比乳酸乳杆菌LM0230更稳定。该稳定性通过缺失3.1kbp的PvuII-XbaI片段而失去,该片段对乳酸乳球菌LM0230的稳定性没有影响。还确定了影响cremoris EB5而不影响乳酸乳球菌LM0230稳定性的其他区域。在各种温度下进行的稳定性分析表明,pKMP1的维持在乳酸乳球菌LM0230和cremoris EB5中都是温度敏感的,尽管质粒在乳酸乳球菌LM0230中更不稳定。乳酸乳球菌LM0230中负责温度敏感性表型的区域暂时定位在1.2kbp ClaI-HindIII片段上,该片段不同于pSK11L的复制区域。我们的结果表明,密切相关的乳酸乳球菌和cremoris乳杆菌亚种在维持质粒方面表现不同。

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