Comparative Genomic Evidence for a Close Relationship between the Dimorphic Prosthecate Bacteria Hyphomonas neptunium and Caulobacter crescentus

Author:

Badger Jonathan H.1,Hoover Timothy R.2,Brun Yves V.3,Weiner Ronald M.4,Laub Michael T.5,Alexandre Gladys6,Mrázek Jan2,Ren Qinghu1,Paulsen Ian T.1,Nelson Karen E.1,Khouri Hoda M.1,Radune Diana1,Sosa Julia1,Dodson Robert J.1,Sullivan Steven A.1,Rosovitz M. J.1,Madupu Ramana1,Brinkac Lauren M.1,Durkin A. Scott1,Daugherty Sean C.1,Kothari Sagar P.1,Giglio Michelle Gwinn1,Zhou Liwei1,Haft Daniel H.1,Selengut Jeremy D.1,Davidsen Tanja M.1,Yang Qi1,Zafar Nikhat1,Ward Naomi L.17

Affiliation:

1. The Institute for Genomic Research, Rockville, Maryland 20850

2. Department of Microbiology, University of Georgia, Athens, Georgia 30602

3. Department of Biology, Indiana University, Bloomington, Indiana 47405

4. Department of Cell Biology and Molecular Genetics, University of Maryland, College Park, Maryland 20742

5. Bauer Center for Genomics Research, Harvard University, Cambridge, Massachusetts 02138

6. Department of Biochemistry, Cellular and Molecular Biology and Microbiology, University of Tennessee, Knoxville, Tennessee 37996

7. Center of Marine Biotechnology, Baltimore, Maryland 21202

Abstract

ABSTRACT The dimorphic prosthecate bacteria (DPB) are α-proteobacteria that reproduce in an asymmetric manner rather than by binary fission and are of interest as simple models of development. Prior to this work, the only member of this group for which genome sequence was available was the model freshwater organism Caulobacter crescentus . Here we describe the genome sequence of Hyphomonas neptunium , a marine member of the DPB that differs from C. crescentus in that H. neptunium uses its stalk as a reproductive structure. Genome analysis indicates that this organism shares more genes with C. crescentus than it does with Silicibacter pomeroyi (a closer relative according to 16S rRNA phylogeny), that it relies upon a heterotrophic strategy utilizing a wide range of substrates, that its cell cycle is likely to be regulated in a similar manner to that of C. crescentus , and that the outer membrane complements of H. neptunium and C. crescentus are remarkably similar. H. neptunium swarmer cells are highly motile via a single polar flagellum. With the exception of cheY and cheR , genes required for chemotaxis were absent in the H. neptunium genome. Consistent with this observation, H. neptunium swarmer cells did not respond to any chemotactic stimuli that were tested, which suggests that H. neptunium motility is a random dispersal mechanism for swarmer cells rather than a stimulus-controlled navigation system for locating specific environments. In addition to providing insights into bacterial development, the H. neptunium genome will provide an important resource for the study of other interesting biological processes including chromosome segregation, polar growth, and cell aging.

Publisher

American Society for Microbiology

Subject

Molecular Biology,Microbiology

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