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本文引用的文献

1
Improved medium for lactic streptococci and their bacteriophages.用于乳酸链球菌及其噬菌体的改良培养基。
Appl Microbiol. 1975 Jun;29(6):807-13. doi: 10.1128/am.29.6.807-813.1975.
2
Temporally Regulated Transcriptional Expression of the Genomes of Lactococcal Bacteriophages c2 and sk1.乳酸菌噬菌体 c2 和 sk1 基因组的时间调节转录表达。
Appl Environ Microbiol. 1993 Nov;59(11):3708-12. doi: 10.1128/aem.59.11.3708-3712.1993.
3
Rapid method to characterize lactococcal bacteriophage genomes.快速鉴定乳球菌噬菌体基因组的方法。
Appl Environ Microbiol. 1991 Jan;57(1):283-8. doi: 10.1128/aem.57.1.283-288.1991.
4
High-Frequency Transformation, by Electroporation, of Lactococcus lactis subsp. cremoris Grown with Glycine in Osmotically Stabilized Media.在渗透压稳定的培养基中用甘氨酸培养的乳球菌乳亚种经电穿孔高频转化。
Appl Environ Microbiol. 1989 Dec;55(12):3119-23. doi: 10.1128/aem.55.12.3119-3123.1989.
5
Dramatic decay of phage transcripts in lactococcal cells carrying the abortive infection determinant AbiB.
Mol Microbiol. 1996 Jan;19(2):221-30. doi: 10.1046/j.1365-2958.1996.371896.x.
6
Sequence analysis and molecular characterization of the temperate lactococcal bacteriophage r1t.温和型乳酸乳球菌噬菌体r1t的序列分析与分子特征
Mol Microbiol. 1996 Mar;19(6):1343-55. doi: 10.1111/j.1365-2958.1996.tb02478.x.
7
Cloning and DNA sequence analysis of two abortive infection phage resistance determinants from the lactococcal plasmid pNP40.来自乳球菌质粒pNP40的两个流产感染噬菌体抗性决定簇的克隆及DNA序列分析。
Appl Environ Microbiol. 1995 Dec;61(12):4321-8. doi: 10.1128/aem.61.12.4321-4328.1995.
8
Organization and regulation of genes for amino acid biosynthesis in lactic acid bacteria.乳酸菌中氨基酸生物合成基因的组织与调控
FEMS Microbiol Rev. 1993 Sep;12(1-3):21-37. doi: 10.1111/j.1574-6976.1993.tb00011.x.
9
Analysis of the cos region of the Lactococcus lactis bacteriophage sk1.
Gene. 1994 Jan 28;138(1-2):123-6. doi: 10.1016/0378-1119(94)90793-5.
10
Genomic polymorphism in the T-even bacteriophages.T偶数噬菌体中的基因组多态性。
EMBO J. 1994 Sep 1;13(17):4181-92. doi: 10.1002/j.1460-2075.1994.tb06736.x.

乳酸乳球菌噬菌体一个晚期表达区域的基因组织与转录

Gene organization and transcription of a late-expressed region of a Lactococcus lactis phage.

作者信息

Parreira R, Valyasevi R, Lerayer A L, Ehrlich S D, Chopin M C

机构信息

Institut National de la Recherche Agronomique, Laboratoire de Génétique Microbienne, Jouy-en-Josas, France.

出版信息

J Bacteriol. 1996 Nov;178(21):6158-65. doi: 10.1128/jb.178.21.6158-6165.1996.

DOI:10.1128/jb.178.21.6158-6165.1996
PMID:8892814
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC178485/
Abstract

The lactococcal phage bIL41 belongs to the small isometric-headed phages of the 936 quasi-species and is resistant to the abortive infection determined by abiB. A 10.2-kb segment from this phage, in which late transcription is initiated, has been sequenced. Thirteen open reading frames (ORFs) organized in one transcriptional unit have been identified. The location of two of them and the structural features of the proteins they code for are evocative of terminase subunits. Five other ORFs specify proteins which are highly homologous to structural proteins from the closely related phage F4-1. By comparing the phage bIL41 sequence with partial sequences available for four related phages, we were able to deduce a chimerical phage map covering the middle- and a large part of the late-expressed regions. Phages from this quasi-species differ by the insertion or deletion of either 1 to about 400 bp in noncoding regions or an entire ORF. Transcription was initiated 9 min after infection at a promoter with a -10 but no -35 consensus sequence. Synthesis of a phage activator protein was needed for initiation of transcription. A large 16-kb transcript covering all of the late-expressed region of the genome was synthesized. This transcript gave rise to smaller units. One of these units most probably resulted from a RNase E processing.

摘要

乳球菌噬菌体bIL41属于936准种的小等轴头噬菌体,对abiB决定的流产感染具有抗性。已对该噬菌体中启动晚期转录的一个10.2 kb片段进行了测序。已鉴定出在一个转录单元中组织的13个开放阅读框(ORF)。其中两个的位置及其编码蛋白质的结构特征让人联想到末端酶亚基。其他五个ORF指定的蛋白质与密切相关的噬菌体F4-1的结构蛋白质高度同源。通过将噬菌体bIL41序列与四个相关噬菌体的部分序列进行比较,我们能够推导出一个涵盖中期和大部分晚期表达区域的嵌合噬菌体图谱。该准种的噬菌体在非编码区或整个ORF中存在1至约400 bp的插入或缺失差异。感染后9分钟,转录在一个具有-10但无-35共有序列的启动子处开始。转录起始需要噬菌体激活蛋白的合成。合成了一个覆盖基因组所有晚期表达区域的16 kb大转录本。该转录本产生了较小的单元。其中一个单元很可能是由核糖核酸酶E加工产生的。