Genomics-Guided Exploitation of Lipopeptide Diversity in Myxobacteria
Analysis of 122 myxobacterial genome sequences suggested 16 strains as producers of the myxochromide lipopeptide family. Detailed sequence comparison of the respective mch biosynthetic gene clusters informed a genome-mining approach, ultimately leading to the discovery and chemical characterization...
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Published in | ACS Chemical Biology Vol. 12; no. 3; pp. 779 - 786 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
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United States
American Chemical Society
17.03.2017
American Chemical Society (ACS) |
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Abstract | Analysis of 122 myxobacterial genome sequences suggested 16 strains as producers of the myxochromide lipopeptide family. Detailed sequence comparison of the respective mch biosynthetic gene clusters informed a genome-mining approach, ultimately leading to the discovery and chemical characterization of four novel myxochromide core types. The myxochromide megasynthetase is subject to evolutionary diversification, resulting in considerable structural diversity of biosynthesis products. The observed differences are due to the number, type, sequence, and configuration of the incorporated amino acids. The analysis revealed molecular details on how point mutations and recombination events led to structural diversity. It also gave insights into the evolutionary scenarios that have led to the emergence of mch clusters in different strains and genera of myxobacteria. |
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AbstractList | Analysis of 122 myxobacterial genome sequences suggested 16 strains as producers of the myxochromide lipopeptide family. Detailed sequence comparison of the respective mch biosynthetic gene clusters informed a genome-mining approach, ultimately leading to the discovery and chemical characterization of four novel myxochromide core types. The myxochromide megasynthetase is subject to evolutionary diversification, resulting in considerable structural diversity of biosynthesis products. The observed differences are due to the number, type, sequence, and configuration of the incorporated amino acids. The analysis revealed molecular details on how point mutations and recombination events led to structural diversity. It also gave insights into the evolutionary scenarios that have led to the emergence of mch clusters in different strains and genera of myxobacteria.Analysis of 122 myxobacterial genome sequences suggested 16 strains as producers of the myxochromide lipopeptide family. Detailed sequence comparison of the respective mch biosynthetic gene clusters informed a genome-mining approach, ultimately leading to the discovery and chemical characterization of four novel myxochromide core types. The myxochromide megasynthetase is subject to evolutionary diversification, resulting in considerable structural diversity of biosynthesis products. The observed differences are due to the number, type, sequence, and configuration of the incorporated amino acids. The analysis revealed molecular details on how point mutations and recombination events led to structural diversity. It also gave insights into the evolutionary scenarios that have led to the emergence of mch clusters in different strains and genera of myxobacteria. Analysis of 122 myxobacterial genome sequences suggested 16 strains as producers of the myxochromide lipopeptide family. Detailed sequence comparison of the respective mch biosynthetic gene clusters informed a genome-mining approach, ultimately leading to the discovery and chemical characterization of four novel myxochromide core types. The myxochromide megasynthetase is subject to evolutionary diversification, resulting in considerable structural diversity of biosynthesis products. The observed differences are due to the number, type, sequence, and configuration of the incorporated amino acids. The analysis revealed molecular details on how point mutations and recombination events led to structural diversity. It also gave insights into the evolutionary scenarios that have led to the emergence of mch clusters in different strains and genera of myxobacteria. |
Author | Zaburannyi, Nestor Wenzel, Silke C Luxenburger, Eva Maier, Josef Jenke-Kodama, Holger Bernauer, Hubert S Burgard, Christian Nadmid, Suvd |
AuthorAffiliation | Okinawa Institute of Science and Technology (OIST) IStLS − Information Services to Life Sciences Helmholtz Institute for Pharmaceutical Research Saarland (HIPS), Helmholtz Centre for Infection Research and Pharmaceutical Biotechnology at Saarland University ATG Biosynthetics GmbH Microbiology and Biochemistry of Secondary Metabolites Unit |
AuthorAffiliation_xml | – name: Helmholtz Institute for Pharmaceutical Research Saarland (HIPS), Helmholtz Centre for Infection Research and Pharmaceutical Biotechnology at Saarland University – name: Microbiology and Biochemistry of Secondary Metabolites Unit – name: IStLS − Information Services to Life Sciences – name: Okinawa Institute of Science and Technology (OIST) – name: ATG Biosynthetics GmbH |
Author_xml | – sequence: 1 givenname: Christian surname: Burgard fullname: Burgard, Christian organization: Helmholtz Institute for Pharmaceutical Research Saarland (HIPS), Helmholtz Centre for Infection Research and Pharmaceutical Biotechnology at Saarland University – sequence: 2 givenname: Nestor surname: Zaburannyi fullname: Zaburannyi, Nestor organization: Helmholtz Institute for Pharmaceutical Research Saarland (HIPS), Helmholtz Centre for Infection Research and Pharmaceutical Biotechnology at Saarland University – sequence: 3 givenname: Suvd surname: Nadmid fullname: Nadmid, Suvd organization: Helmholtz Institute for Pharmaceutical Research Saarland (HIPS), Helmholtz Centre for Infection Research and Pharmaceutical Biotechnology at Saarland University – sequence: 4 givenname: Josef surname: Maier fullname: Maier, Josef organization: IStLS − Information Services to Life Sciences – sequence: 5 givenname: Holger surname: Jenke-Kodama fullname: Jenke-Kodama, Holger organization: Okinawa Institute of Science and Technology (OIST) – sequence: 6 givenname: Eva surname: Luxenburger fullname: Luxenburger, Eva organization: Helmholtz Institute for Pharmaceutical Research Saarland (HIPS), Helmholtz Centre for Infection Research and Pharmaceutical Biotechnology at Saarland University – sequence: 7 givenname: Hubert S surname: Bernauer fullname: Bernauer, Hubert S organization: ATG Biosynthetics GmbH – sequence: 8 givenname: Silke C orcidid: 0000-0002-3626-795X surname: Wenzel fullname: Wenzel, Silke C email: silke.wenzel@helmholtz-hzi.de organization: Helmholtz Institute for Pharmaceutical Research Saarland (HIPS), Helmholtz Centre for Infection Research and Pharmaceutical Biotechnology at Saarland University |
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SubjectTerms | Genomics Lipopeptides Lipopeptides - metabolism Multigene Family Myxococcales Myxococcales - genetics Myxococcales - metabolism |
Title | Genomics-Guided Exploitation of Lipopeptide Diversity in Myxobacteria |
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