Literature DB >> 26655756

Multiple Posttranslational Modifications of Leptospira biflexa Proteins as Revealed by Proteomic Analysis.

Philip E Stewart1, James A Carroll2, L Rennee Olano3, Daniel E Sturdevant4, Patricia A Rosa5.   

Abstract

The saprophyte Leptospira biflexa is an excellent model for studying the physiology of the medically important Leptospira genus, the pathogenic members of which are more recalcitrant to genetic manipulation and have significantly slower in vitro growth. However, relatively little is known regarding the proteome of L. biflexa, limiting its utility as a model for some studies. Therefore, we have generated a proteomic map of both soluble and membrane-associated proteins of L. biflexa during exponential growth and in stationary phase. Using these data, we identified abundantly produced proteins in each cellular fraction and quantified the transcript levels from a subset of these genes using quantitative reverse transcription-PCR (RT-PCR). These proteins should prove useful as cellular markers and as controls for gene expression studies. We also observed a significant number of L. biflexa membrane-associated proteins with multiple isoforms, each having unique isoelectric focusing points. L. biflexa cell lysates were examined for several posttranslational modifications suggested by the protein patterns. Methylation and acetylation of lysine residues were predominately observed in the proteins of the membrane-associated fraction, while phosphorylation was detected mainly among soluble proteins. These three posttranslational modification systems appear to be conserved between the free-living species L. biflexa and the pathogenic species Leptospira interrogans, suggesting an important physiological advantage despite the varied life cycles of the different species.
Copyright © 2016, American Society for Microbiology. All Rights Reserved.

Entities:  

Mesh:

Substances:

Year:  2015        PMID: 26655756      PMCID: PMC4751834          DOI: 10.1128/AEM.03056-15

Source DB:  PubMed          Journal:  Appl Environ Microbiol        ISSN: 0099-2240            Impact factor:   4.792


  62 in total

1.  Methylation and in vivo expression of the surface-exposed Leptospira interrogans outer-membrane protein OmpL32.

Authors:  Azad Eshghi; Marija Pinne; David A Haake; Richard L Zuerner; Ami Frank; Caroline E Cameron
Journal:  Microbiology       Date:  2011-12-15       Impact factor: 2.777

2.  Expanding the genetic toolbox for Leptospira species by generation of fluorescent bacteria.

Authors:  Florence Aviat; Leyla Slamti; Gustavo M Cerqueira; Kristel Lourdault; Mathieu Picardeau
Journal:  Appl Environ Microbiol       Date:  2010-10-29       Impact factor: 4.792

3.  Serologic proteome analysis of Borrelia burgdorferi membrane-associated proteins.

Authors:  Andrew J Nowalk; Robert D Gilmore; James A Carroll
Journal:  Infect Immun       Date:  2006-07       Impact factor: 3.441

4.  Inactivation of clpB in the pathogen Leptospira interrogans reduces virulence and resistance to stress conditions.

Authors:  Kristel Lourdault; Gustavo M Cerqueira; Elsio A Wunder; Mathieu Picardeau
Journal:  Infect Immun       Date:  2011-07-05       Impact factor: 3.441

5.  Protein acetylation in prokaryotes increases stress resistance.

Authors:  Qun Ma; Thomas K Wood
Journal:  Biochem Biophys Res Commun       Date:  2011-06-15       Impact factor: 3.575

6.  Insight into the virulence of Rickettsia prowazekii by proteomic analysis and comparison with an avirulent strain.

Authors:  Chien-Chung Chao; Dirk Chelius; Terry Zhang; Elissa Mutumanje; Wei-Mei Ching
Journal:  Biochim Biophys Acta       Date:  2007-01-17

7.  Acetylation of metabolic enzymes coordinates carbon source utilization and metabolic flux.

Authors:  Qijun Wang; Yakun Zhang; Chen Yang; Hui Xiong; Yan Lin; Jun Yao; Hong Li; Lu Xie; Wei Zhao; Yufeng Yao; Zhi-Bin Ning; Rong Zeng; Yue Xiong; Kun-Liang Guan; Shimin Zhao; Guo-Ping Zhao
Journal:  Science       Date:  2010-02-19       Impact factor: 47.728

8.  Leptospira spp. possess a complete haem biosynthetic pathway and are able to use exogenous haem sources.

Authors:  Rozenn Guégan; Jean-Michel Camadro; Isabelle Saint Girons; Mathieu Picardeau
Journal:  Mol Microbiol       Date:  2003-08       Impact factor: 3.501

9.  Mycobacterial heparin-binding hemagglutinin and laminin-binding protein share antigenic methyllysines that confer resistance to proteolysis.

Authors:  Kevin Pethe; Pablo Bifani; Hervé Drobecq; Christian Sergheraert; Anne-Sophie Debrie; Camille Locht; Franco D Menozzi
Journal:  Proc Natl Acad Sci U S A       Date:  2002-07-29       Impact factor: 11.205

10.  The diversity of lysine-acetylated proteins in Escherichia coli.

Authors:  Byung Jo Yu; Jung Ae Kim; Jeong Hee Moon; Seong Eon Ryu; Jae-Gu Pan
Journal:  J Microbiol Biotechnol       Date:  2008-09       Impact factor: 2.351

View more
  7 in total

1.  A widely conserved bacterial cytoskeletal component influences unique helical shape and motility of the spirochete Leptospira biflexa.

Authors:  Katrina M Jackson; Cindi Schwartz; Jenny Wachter; Patricia A Rosa; Philip E Stewart
Journal:  Mol Microbiol       Date:  2018-02-13       Impact factor: 3.501

2.  Unique Posttranslational Modification Sites of Acetylation, Citrullination, Glutarylation, and Phosphorylation Are Found to Be Specific to the Proteins Partitioned in the Triton X-114 Fractions of Leptospira.

Authors:  Homen Phukan; Abhijit Sarma; Devasahayam Arokia Balaya Rex; Akhila Balakrishna Rai; Thottethodi Subrahmanya Keshava Prasad; Madathiparambil Gopalakrishnan Madanan
Journal:  ACS Omega       Date:  2022-05-25

3.  The sigma factor σ54 is required for the long-term survival of Leptospira biflexa in water.

Authors:  Jun-Jie Zhang; Wei-Lin Hu; Youyun Yang; Hongxia Li; Mathieu Picardeau; Jie Yan; X Frank Yang
Journal:  Mol Microbiol       Date:  2018-04-06       Impact factor: 3.501

4.  Pathogenic Leptospires Modulate Protein Expression and Post-translational Modifications in Response to Mammalian Host Signals.

Authors:  Jarlath E Nally; Andre A Grassmann; Sébastien Planchon; Kjell Sergeant; Jenny Renaut; Janakiram Seshu; Alan J McBride; Melissa J Caimano
Journal:  Front Cell Infect Microbiol       Date:  2017-08-09       Impact factor: 5.293

5.  Visualization of Spirochetes by Labeling Membrane Proteins With Fluorescent Biarsenical Dyes.

Authors:  Chadwick Hillman; Philip E Stewart; Martin Strnad; Hunter Stone; Tregei Starr; Aaron Carmody; Tyler J Evans; Valentina Carracoi; Jenny Wachter; Patricia A Rosa
Journal:  Front Cell Infect Microbiol       Date:  2019-08-20       Impact factor: 5.293

Review 6.  The Diverse Functional Roles of Elongation Factor Tu (EF-Tu) in Microbial Pathogenesis.

Authors:  Kate L Harvey; Veronica M Jarocki; Ian G Charles; Steven P Djordjevic
Journal:  Front Microbiol       Date:  2019-10-24       Impact factor: 5.640

7.  FcpB Is a Surface Filament Protein of the Endoflagellum Required for the Motility of the Spirochete Leptospira.

Authors:  Elsio A Wunder; Leyla Slamti; David N Suwondo; Kimberley H Gibson; Zhiguo Shang; Charles V Sindelar; Felipe Trajtenberg; Alejandro Buschiazzo; Albert I Ko; Mathieu Picardeau
Journal:  Front Cell Infect Microbiol       Date:  2018-05-08       Impact factor: 5.293

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.