Engineering microbial hosts for production of bacterial natural products
Covering up to end 2015 Microbial fermentation provides an attractive alternative to chemical synthesis for the production of structurally complex natural products. In most cases, however, production titers are low and need to be improved for compound characterization and/or commercial production. O...
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Veröffentlicht in: | Natural product reports 2016-08, Vol.33 (8), p.963-987 |
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creator | Zhang, Mingzi M Wang, Yajie Ang, Ee Lui Zhao, Huimin |
description | Covering up to end 2015
Microbial fermentation provides an attractive alternative to chemical synthesis for the production of structurally complex natural products. In most cases, however, production titers are low and need to be improved for compound characterization and/or commercial production. Owing to advances in functional genomics and genetic engineering technologies, microbial hosts can be engineered to overproduce a desired natural product, greatly accelerating the traditionally time-consuming strain improvement process. This review covers recent developments and challenges in the engineering of native and heterologous microbial hosts for the production of bacterial natural products, focusing on the genetic tools and strategies for strain improvement. Special emphasis is placed on bioactive secondary metabolites from actinomycetes. The considerations for the choice of host systems will also be discussed in this review.
Microbial fermentation provides an attractive alternative to chemical synthesis for the production of structurally complex natural products. |
doi_str_mv | 10.1039/c6np00017g |
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Microbial fermentation provides an attractive alternative to chemical synthesis for the production of structurally complex natural products. In most cases, however, production titers are low and need to be improved for compound characterization and/or commercial production. Owing to advances in functional genomics and genetic engineering technologies, microbial hosts can be engineered to overproduce a desired natural product, greatly accelerating the traditionally time-consuming strain improvement process. This review covers recent developments and challenges in the engineering of native and heterologous microbial hosts for the production of bacterial natural products, focusing on the genetic tools and strategies for strain improvement. Special emphasis is placed on bioactive secondary metabolites from actinomycetes. The considerations for the choice of host systems will also be discussed in this review.
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Microbial fermentation provides an attractive alternative to chemical synthesis for the production of structurally complex natural products. In most cases, however, production titers are low and need to be improved for compound characterization and/or commercial production. Owing to advances in functional genomics and genetic engineering technologies, microbial hosts can be engineered to overproduce a desired natural product, greatly accelerating the traditionally time-consuming strain improvement process. This review covers recent developments and challenges in the engineering of native and heterologous microbial hosts for the production of bacterial natural products, focusing on the genetic tools and strategies for strain improvement. Special emphasis is placed on bioactive secondary metabolites from actinomycetes. The considerations for the choice of host systems will also be discussed in this review.
Microbial fermentation provides an attractive alternative to chemical synthesis for the production of structurally complex natural products.</description><subject>Actinobacteria</subject><subject>Actinomyces - chemistry</subject><subject>Bacteria</subject><subject>Bacteria - chemistry</subject><subject>Biological Products - metabolism</subject><subject>engineering</subject><subject>fermentation</subject><subject>Genetic Engineering</subject><subject>genomics</subject><subject>hosts</subject><subject>Molecular Structure</subject><subject>secondary metabolites</subject><subject>synthesis</subject><issn>0265-0568</issn><issn>1460-4752</issn><issn>1460-4752</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNks1LJDEQxYO46Dh68a70cRF6raQ7H30RZNBxQVYPeg5JOj0TmUnGpFvwv9-sMzvqSU8F9X48quoVQscYfmGomnPD_AoAMJ_toBGuGZQ1p2QXjYAwWgJlYh8dpPSUEcwZ20P7hAMnAuoRurnyM-etjc7PiqUzMWinFsU8pD4VXYjFKoZ2ML0LvghdoZXpM5sJr_oh5rrR0yH60alFskebOkaP11cPk5vy9m76e3J5WxrKq77U2ljd1YRg0VINVllueFOD5ZQ2wHWrOsOAC8II7izhjFLdEMzb1tjOClaN0cXadzXopc1d3-cx5Cq6pYqvMignPyvezeUsvMi6YRXhPBv83BjE8DzY1MulS8YuFsrbMCRJCMcCoMqn_QrFAmMhSE3pN9C8VAMNqTJ6tkbzsVOKttsOj0H-C1RO2J_7t0CnGT79uO4W_Z9gBk7WQExmq75_RPUXqyemhQ</recordid><startdate>20160827</startdate><enddate>20160827</enddate><creator>Zhang, Mingzi M</creator><creator>Wang, Yajie</creator><creator>Ang, Ee Lui</creator><creator>Zhao, Huimin</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7QL</scope><scope>7QO</scope><scope>7T7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>7S9</scope><scope>L.6</scope><scope>5PM</scope></search><sort><creationdate>20160827</creationdate><title>Engineering microbial hosts for production of bacterial natural products</title><author>Zhang, Mingzi M ; Wang, Yajie ; Ang, Ee Lui ; Zhao, Huimin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c573t-bbcebf42218d5b0eae7c7940e755907bdafc60782621fe27655b9217ddcefe863</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Actinobacteria</topic><topic>Actinomyces - chemistry</topic><topic>Bacteria</topic><topic>Bacteria - chemistry</topic><topic>Biological Products - metabolism</topic><topic>engineering</topic><topic>fermentation</topic><topic>Genetic Engineering</topic><topic>genomics</topic><topic>hosts</topic><topic>Molecular Structure</topic><topic>secondary metabolites</topic><topic>synthesis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhang, Mingzi M</creatorcontrib><creatorcontrib>Wang, Yajie</creatorcontrib><creatorcontrib>Ang, Ee Lui</creatorcontrib><creatorcontrib>Zhao, Huimin</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Natural product reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhang, Mingzi M</au><au>Wang, Yajie</au><au>Ang, Ee Lui</au><au>Zhao, Huimin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Engineering microbial hosts for production of bacterial natural products</atitle><jtitle>Natural product reports</jtitle><addtitle>Nat Prod Rep</addtitle><date>2016-08-27</date><risdate>2016</risdate><volume>33</volume><issue>8</issue><spage>963</spage><epage>987</epage><pages>963-987</pages><issn>0265-0568</issn><issn>1460-4752</issn><eissn>1460-4752</eissn><abstract>Covering up to end 2015
Microbial fermentation provides an attractive alternative to chemical synthesis for the production of structurally complex natural products. In most cases, however, production titers are low and need to be improved for compound characterization and/or commercial production. Owing to advances in functional genomics and genetic engineering technologies, microbial hosts can be engineered to overproduce a desired natural product, greatly accelerating the traditionally time-consuming strain improvement process. This review covers recent developments and challenges in the engineering of native and heterologous microbial hosts for the production of bacterial natural products, focusing on the genetic tools and strategies for strain improvement. Special emphasis is placed on bioactive secondary metabolites from actinomycetes. The considerations for the choice of host systems will also be discussed in this review.
Microbial fermentation provides an attractive alternative to chemical synthesis for the production of structurally complex natural products.</abstract><cop>England</cop><pmid>27072804</pmid><doi>10.1039/c6np00017g</doi><tpages>25</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection |
subjects | Actinobacteria Actinomyces - chemistry Bacteria Bacteria - chemistry Biological Products - metabolism engineering fermentation Genetic Engineering genomics hosts Molecular Structure secondary metabolites synthesis |
title | Engineering microbial hosts for production of bacterial natural products |
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