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乳酸乳球菌 pLY101 质粒的性质。

Properties of Lactose Plasmid pLY101 in Lactobacillus casei.

机构信息

Yakult Central Institute for Microbiological Research, 1796 Yaho, Kunitachi, Tokyo 186, Japan.

出版信息

Appl Environ Microbiol. 1987 Dec;53(12):2987-91. doi: 10.1128/aem.53.12.2987-2991.1987.

Abstract

A starter strain, Lactobacillus casei C257, was found to carry a lactose plasmid, pLY101. Restriction mapping showed that pLY101 DNA was 68.2 kilobases long. Since a non-lactose-utilizing variant of C257, MSK248, lost phospho-beta-galactosidase (P-beta-gal) activity and pLY101 DNA had a sequence(s) homologous to the streptococcal fragment including a P-beta-gal gene, pLY101 is likely to encode a P-beta-gal gene required for lactose metabolism in C257. MSK248 grew in galactose medium at a rate identical to that of C257 and retained phosphoenolpyruvate-dependent phosphotransferase system activity for lactose similar to that of C257. Therefore, the C257 chromosome appears to encode a complete set of genes for the lactose-phosphotransferase system and the predominant galactose metabolic pathway in C257. pLY101 DNA had a sequence homologous to a lactobacillus insertion sequence, ISL1, which mapped more than 12 kilobases from the sequence homologous to the streptococcal P-beta-gal fragment.

摘要

起始菌株干酪乳杆菌 C257 携带乳糖质体 pLY101。限制图谱显示,pLY101 DNA 长 68.2 千碱基。由于 C257 的一个非乳糖利用突变株 MSK248 丧失了磷酸-β-半乳糖苷酶(P-β-gal)活性,而且 pLY101 DNA 序列与包括 P-β-gal 基因的链球片段同源,所以 pLY101 可能编码乳糖代谢所必需的 P-β-gal 基因。MSK248 在半乳糖培养基中生长的速度与 C257 相同,并且保持与 C257 相似的磷酸烯醇丙酮酸依赖性磷酸转移酶系统对乳糖的活性。因此,C257 染色体似乎编码乳糖磷酸转移酶系统和 C257 中主要的半乳糖代谢途径的整套基因。pLY101 DNA 与乳杆菌插入序列 ISL1 序列同源,该序列与链球 P-β-gal 片段的同源序列相差 12 千碱基以上。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fb8/204236/9e63f4f5da47/aem00129-0301-a.jpg

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