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原生质体诱导消除后乳酸乳球菌NCDO 712及其他乳酸链球菌的质粒互补体

Plasmid complements of Streptococcus lactis NCDO 712 and other lactic streptococci after protoplast-induced curing.

作者信息

Gasson M J

出版信息

J Bacteriol. 1983 Apr;154(1):1-9. doi: 10.1128/jb.154.1.1-9.1983.

Abstract

The production and regeneration of bacterial protoplasts promoted the loss of three different plasmid-specified traits in Streptococcus lactis subsp. diacetylactis strains. The loss of five different plasmids, including small multicopy molecules, was readily detected in Streptococcus lactis 712 by screening lysates of random protoplast regenerants on agarose gels. In this strain sequential rounds of protoplast regeneration were used to produce a plasmid-free strain and derivatives carrying only single molecules from the plasmid complement. During these experiments a 33-megadalton plasmid, pLP712, was found to encode genes for lactose and protein utilization. Only this plasmid was required for normal growth and acid production in milk; the remaining four plasmids appeared to be cryptic. Lactose-defective derivatives of a strain carrying only pLP712 were readily isolated. Although these derivatives included instances of plasmid loss, deletions of pLP712 were frequently found. Many different deleted derivatives of pLP712, including some in which the lactose or protein utilization determinant or both were lost, were isolated. The molecular instability of pLP712 largely accounted for previous observations of plasmid complements in S. lactis 712 after lactose determinant curing or transfer by conjugation and transduction. Curing of cryptic molecules from multiple plasmid complements by protoplast regeneration may prove to be generally valuable in lactic streptococci and other gram-positive species.

摘要

细菌原生质体的产生和再生促进了乳酸乳球菌亚种双乙酰乳酸菌株中三种不同质粒指定性状的丧失。通过在琼脂糖凝胶上筛选随机原生质体再生体的裂解物,很容易检测到乳酸乳球菌712中五种不同质粒(包括小型多拷贝分子)的丧失。在该菌株中,连续几轮原生质体再生被用于产生无质粒菌株和仅携带质粒互补物中单个分子的衍生物。在这些实验中,发现一个33兆道尔顿的质粒pLP712编码乳糖和蛋白质利用的基因。只有该质粒是在牛奶中正常生长和产酸所必需的;其余四种质粒似乎是隐蔽的。很容易分离出仅携带pLP712的菌株的乳糖缺陷衍生物。虽然这些衍生物包括质粒丢失的情况,但经常发现pLP712的缺失。分离出了许多不同的pLP712缺失衍生物,包括一些乳糖或蛋白质利用决定因素或两者都丢失的衍生物。pLP712的分子不稳定性在很大程度上解释了先前在乳糖决定因素治愈或通过接合和转导转移后乳酸乳球菌712中质粒互补物的观察结果。通过原生质体再生从多个质粒互补物中去除隐蔽分子可能在乳酸链球菌和其他革兰氏阳性菌中普遍具有价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6dac/217423/ef001507c7f2/jbacter00245-0014-a.jpg

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