Literature DB >> 25896738

Comprehensive proteome analysis of Actinoplanes sp. SE50/110 highlighting the location of proteins encoded by the acarbose and the pyochelin biosynthesis gene cluster.

Sergej Wendler1, Andreas Otto2, Vera Ortseifen3, Florian Bonn2, Armin Neshat4, Susanne Schneiker-Bekel5, Frederik Walter6, Timo Wolf3, Till Zemke7, Udo F Wehmeier8, Michael Hecker2, Jörn Kalinowski4, Dörte Becher2, Alfred Pühler5.   

Abstract

Acarbose is an α-glucosidase inhibitor produced by Actinoplanes sp. SE50/110 that is medically important due to its application in the treatment of type2 diabetes. In this work, a comprehensive proteome analysis of Actinoplanes sp. SE50/110 was carried out to determine the location of proteins of the acarbose (acb) and the putative pyochelin (pch) biosynthesis gene cluster. Therefore, a comprehensive state-of-the-art proteomics approach combining subcellular fractionation, shotgun proteomics and spectral counting to assess the relative abundance of proteins within fractions was applied. The analysis of four different proteome fractions (cytosolic, enriched membrane, membrane shaving and extracellular fraction) resulted in the identification of 1582 of the 8270 predicted proteins. All 22 Acb-proteins and 21 of the 23 Pch-proteins were detected. Predicted membrane-associated, integral membrane or extracellular proteins of the pch and the acb gene cluster were found among the most abundant proteins in corresponding fractions. Intracellular biosynthetic proteins of both gene clusters were not only detected in the cytosolic, but also in the enriched membrane fraction, indicating that the biosynthesis of acarbose and putative pyochelin metabolites takes place at the inner membrane. BIOLOGICAL SIGNIFICANCE: Actinoplanes sp. SE50/110 is a natural producer of the α-glucosidase inhibitor acarbose, a bacterial secondary metabolite that is used as a drug for the treatment of type 2 diabetes, a disease which is a global pandemic that currently affects 387 million people and accounts for 11% of worldwide healthcare expenditures (www.idf.org). The work presented here is the first comprehensive investigation of protein localization and abundance in Actinoplanes sp. SE50/110 and provides an extensive source of information for the selection of genes for future mutational analysis and other hypothesis driven experiments. The conclusion that acarbose or pyochelin family siderophores are synthesized at the inner side of the cytoplasmic membrane determined from this work, indicates that studying corresponding intermediates will be challenging. In addition to previous studies on the genome and transcriptome, the work presented here demonstrates that the next omic level, the proteome, is now accessible for detailed physiological analysis of Actinoplanes sp. SE50/110, as well as mutants derived from this and related species.
Copyright © 2015 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Actinoplanes; Comprehensive proteomics; Membrane proteome acarbose; Pyochelin; Subcellular fractionation

Mesh:

Substances:

Year:  2015        PMID: 25896738     DOI: 10.1016/j.jprot.2015.04.013

Source DB:  PubMed          Journal:  J Proteomics        ISSN: 1874-3919            Impact factor:   4.044


  7 in total

1.  The MalR type regulator AcrC is a transcriptional repressor of acarbose biosynthetic genes in Actinoplanes sp. SE50/110.

Authors:  Timo Wolf; Julian Droste; Tetiana Gren; Vera Ortseifen; Susanne Schneiker-Bekel; Till Zemke; Alfred Pühler; Jörn Kalinowski
Journal:  BMC Genomics       Date:  2017-07-25       Impact factor: 3.969

2.  Comparative functional genomics of the acarbose producers reveals potential targets for metabolic engineering.

Authors:  Huixin Xie; Qinqin Zhao; Xin Zhang; Qianjin Kang; Linquan Bai
Journal:  Synth Syst Biotechnol       Date:  2019-01-18

3.  Absence of the highly expressed small carbohydrate-binding protein Cgt improves the acarbose formation in Actinoplanes sp. SE50/110.

Authors:  Lena Schaffert; Susanne Schneiker-Bekel; Jessica Gierhake; Julian Droste; Marcus Persicke; Winfried Rosen; Alfred Pühler; Jörn Kalinowski
Journal:  Appl Microbiol Biotechnol       Date:  2020-04-28       Impact factor: 4.813

4.  Essentiality of the Maltase AmlE in Maltose Utilization and Its Transcriptional Regulation by the Repressor AmlR in the Acarbose-Producing Bacterium Actinoplanes sp. SE50/110.

Authors:  Lena Schaffert; Susanne Schneiker-Bekel; Saskia Dymek; Julian Droste; Marcus Persicke; Tobias Busche; David Brandt; Alfred Pühler; Jörn Kalinowski
Journal:  Front Microbiol       Date:  2019-10-29       Impact factor: 5.640

5.  The expression of the acarbose biosynthesis gene cluster in Actinoplanes sp. SE50/110 is dependent on the growth phase.

Authors:  Julian Droste; Vera Ortseifen; Lena Schaffert; Marcus Persicke; Susanne Schneiker-Bekel; Alfred Pühler; Jörn Kalinowski
Journal:  BMC Genomics       Date:  2020-11-23       Impact factor: 3.969

6.  Improving acarbose production and eliminating the by-product component C with an efficient genetic manipulation system of Actinoplanes sp. SE50/110.

Authors:  Qinqin Zhao; Huixin Xie; Yao Peng; Xinran Wang; Linquan Bai
Journal:  Synth Syst Biotechnol       Date:  2017-11-27

7.  A maltose-regulated large genomic region is activated by the transcriptional regulator MalT in Actinoplanes sp. SE50/110.

Authors:  Julian Droste; Martin Kulisch; Timo Wolf; Lena Schaffert; Susanne Schneiker-Bekel; Alfred Pühler; Jörn Kalinowski
Journal:  Appl Microbiol Biotechnol       Date:  2020-09-28       Impact factor: 4.813

  7 in total

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