Literature DB >> 26597626

Comparative proteome analysis of Actinoplanes sp. SE50/110 grown with maltose or glucose shows minor differences for acarbose biosynthesis proteins but major differences for saccharide transporters.

Sergej Wendler1, Andreas Otto2, Vera Ortseifen3, Florian Bonn2, Armin Neshat4, Susanne Schneiker-Bekel1, Timo Wolf3, Till Zemke5, Udo F Wehmeier6, Michael Hecker2, Jörn Kalinowski4, Dörte Becher2, Alfred Pühler1.   

Abstract

Actinoplanes sp. SE50/110 is known for the production of the α-glucosidase inhibitor and anti-diabetic drug acarbose. Acarbose (acarviosyl-maltose) is produced as the major product when the bacterium is grown in medium with maltose, while acarviosyl-glucose is the major product when glucose is the sole carbon source in the medium. In this study, a state-of-the-art proteomics approach was applied combining subcellular fractionation, in vivo metabolic labeling and shotgun mass spectrometry to analyze differences in the proteome of Actinoplanes sp. SE50/110 cultures grown in minimal medium containing either maltose or glucose as the sole carbon source. To study proteins in distinct subcellular locations, a cytosolic, an enriched membrane, a membrane shaving and an extracellular fraction were included in the analysis. Altogether, quantitative proteome data was obtained for 2497 proteins representing about 30% of the ca. 8270 predicted proteins of Actinoplanes sp. SE50/110. When comparing protein quantities of maltose- to glucose-grown cultures, differences were observed for saccharide transport and metabolism proteins, whereas differences for acarbose biosynthesis gene cluster proteins were almost absent. The maltose-inducible α-glucosidase/maltase MalL as well as the ABC-type saccharide transporters AglEFG, MalEFG and MstEAF had significantly higher quantities in the maltose growth condition. The only highly abundant saccharide transporter in the glucose condition was the monosaccharide transporter MstEAF, which may indicate that MstEAF is the major glucose importer. Taken all findings together, the previously observed formation of acarviosyl-maltose and acarviosyl-glucose is more closely connected to the transport of saccharides than to a differential expression of the acarbose gene cluster. BIOLOGICAL SIGNIFICANCE: Diabetes is a global pandemic accounting for about 11% of the worldwide healthcare expenditures (>600 billion US dollars) and is projected to affect 592 million people by 2035 (www.idf.org). Whether Actinoplanes sp. SE50/110 produces type 2 diabetes drug acarbose (acarviosyl-maltose) or another acarviose metabolite such as acarviosyl-glucose as the major product depends on the offered carbon source. The differences observed in this proteome in this study suggest that the differences in the formation of acarviosyl-maltose and acarviosyl-glucose are more closely connected to the transport of saccharides than to a differential expression of the acarbose gene cluster. In addition, the present study provides a comprehensive overview of the proteome of Actinoplanes sp. SE50/110.
Copyright © 2015 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Acarbose; Actinoplanes; Comprehensive proteomics; Metabolic labeling; Subcellular fractionation

Mesh:

Substances:

Year:  2015        PMID: 26597626     DOI: 10.1016/j.jprot.2015.10.023

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


  9 in total

1.  Complete biosynthetic pathway to the antidiabetic drug acarbose.

Authors:  Takeshi Tsunoda; Arash Samadi; Sachin Burade; Taifo Mahmud
Journal:  Nat Commun       Date:  2022-06-15       Impact factor: 17.694

2.  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

3.  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

4.  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

5.  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

6.  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

7.  Gene Cascade Shift and Pathway Enrichment in Rat Kidney Induced by Acarbose Through Comparative Analysis.

Authors:  Chun-Yue Weng; Mo-Han Zhu; Ke-Lei Dai; Zhe-Yan Mi; Yuan-Shan Wang; Zhi-Qiang Liu; Yu-Guo Zheng
Journal:  Front Bioeng Biotechnol       Date:  2021-05-21

8.  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

9.  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

  9 in total

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