A cytotoxic early gene of Bacillus subtilis bacteriophage SPO1

Author:

Wei P1,Stewart C R1

Affiliation:

1. Department of Biochemistry and Cell Biology, Rice University, Houston, Texas 77251-1892.

Abstract

Some of the early genes of Bacillus subtilis bacteriophage SPO1 were hypothesized to function in the shutoff of host biosyntheses. Two of these genes, e3 and e22, were cloned and sequenced. E22 showed no similarity to any known protein, while E3, a highly acidic protein, showed significant similarity only to other similarly acidic proteins. Each gene was immediately downstream of a very active early promoter. Each was expressed actively during the first few minutes of infection and was then rapidly shut off and its RNA rapidly degraded. An e3 nonsense mutation severely retarded the degradation of e3 RNA. Expression of a plasmid-borne e3 gene, in either B. subtilis or Escherichia coli, resulted in the inhibition of host DNA, RNA, and protein syntheses and prevented colony formation. However, the e3 nonsense mutation caused no measurable decrease in either burst size or host shutoff during infection and, in fact, caused an increased burst size at high multiplicities of infection. We suggest that e3 is one of several genes involved in host shutoff, that its function is dispensable both for host shutoff and for phage multiplication, and that its shutoff function is not entirely specific to host activities.

Publisher

American Society for Microbiology

Subject

Molecular Biology,Microbiology

Reference72 articles.

1. Basic local alignment search tool;Altschul S. F.;J. Mol. Biol.,1990

2. Deletion analysis of a complex promoter for a developmentally regulated gene from Bacillus subtilis;Banner C. D.;J. Mol. Biol.,1983

3. A transcriptional map of the bacteriophage SPOl genome. II. The major early transcription units;Brennan S. M.;Virology,1981

4. Plasmid deletion formation between short direct repeats in Bacillus subtilis is stimulated by single-stranded rolling-circle replication intermediates;Bron S.;Mol. Gen. Genet.,1991

5. Terminal redundancy of "high frequency of recombination;Cregg J. M.;markers of Bacillus subtilis phage SPOI. Virology,1978

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3