SACE_5599, a putative regulatory protein, is involved in morphological differentiation and erythromycin production in Saccharopolyspora erythraea
Erythromycin is a medically important antibiotic, biosynthesized by the actinomycete Saccharopolyspora erythraea. Genes encoding erythromycin biosynthesis are organized in a gene cluster, spanning over 60 kbp of DNA. Most often, gene clusters encoding biosynthesis of secondary metabolites contain re...
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creator | Kirm, Benjamin Magdevska, Vasilka Tome, Miha Horvat, Marinka Karničar, Katarina Petek, Marko Vidmar, Robert Baebler, Spela Jamnik, Polona Fujs, Štefan Horvat, Jaka Fonovič, Marko Turk, Boris Gruden, Kristina Petković, Hrvoje Kosec, Gregor |
description | Erythromycin is a medically important antibiotic, biosynthesized by the actinomycete Saccharopolyspora erythraea. Genes encoding erythromycin biosynthesis are organized in a gene cluster, spanning over 60 kbp of DNA. Most often, gene clusters encoding biosynthesis of secondary metabolites contain regulatory genes. In contrast, the erythromycin gene cluster does not contain regulatory genes and regulation of its biosynthesis has therefore remained poorly understood, which has for a long time limited genetic engineering approaches for erythromycin yield improvement.
We used a comparative proteomic approach to screen for potential regulatory proteins involved in erythromycin biosynthesis. We have identified a putative regulatory protein SACE_5599 which shows significantly higher levels of expression in an erythromycin high-producing strain, compared to the wild type S. erythraea strain. SACE_5599 is a member of an uncharacterized family of putative regulatory genes, located in several actinomycete biosynthetic gene clusters. Importantly, increased expression of SACE_5599 was observed in the complex fermentation medium and at controlled bioprocess conditions, simulating a high-yield industrial fermentation process in the bioreactor. Inactivation of SACE_5599 in the high-producing strain significantly reduced erythromycin yield, in addition to drastically decreasing sporulation intensity of the SACE_5599-inactivated strains when cultivated on ABSM4 agar medium. In contrast, constitutive overexpression of SACE_5599 in the wild type NRRL23338 strain resulted in an increase of erythromycin yield by 32%. Similar yield increase was also observed when we overexpressed the bldD gene, a previously identified regulator of erythromycin biosynthesis, thereby for the first time revealing its potential for improving erythromycin biosynthesis.
SACE_5599 is the second putative regulatory gene to be identified in S. erythraea which has positive influence on erythromycin yield. Like bldD, SACE_5599 is involved in morphological development of S. erythraea, suggesting a very close relationship between secondary metabolite biosynthesis and morphological differentiation in this organism. While the mode of action of SACE_5599 remains to be elucidated, the manipulation of this gene clearly shows potential for improvement of erythromycin production in S. erythraea in industrial setting. We have also demonstrated the applicability of the comparative proteomics approach for identifying |
doi_str_mv | 10.1186/1475-2859-12-126 |
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We used a comparative proteomic approach to screen for potential regulatory proteins involved in erythromycin biosynthesis. We have identified a putative regulatory protein SACE_5599 which shows significantly higher levels of expression in an erythromycin high-producing strain, compared to the wild type S. erythraea strain. SACE_5599 is a member of an uncharacterized family of putative regulatory genes, located in several actinomycete biosynthetic gene clusters. Importantly, increased expression of SACE_5599 was observed in the complex fermentation medium and at controlled bioprocess conditions, simulating a high-yield industrial fermentation process in the bioreactor. Inactivation of SACE_5599 in the high-producing strain significantly reduced erythromycin yield, in addition to drastically decreasing sporulation intensity of the SACE_5599-inactivated strains when cultivated on ABSM4 agar medium. In contrast, constitutive overexpression of SACE_5599 in the wild type NRRL23338 strain resulted in an increase of erythromycin yield by 32%. Similar yield increase was also observed when we overexpressed the bldD gene, a previously identified regulator of erythromycin biosynthesis, thereby for the first time revealing its potential for improving erythromycin biosynthesis.
SACE_5599 is the second putative regulatory gene to be identified in S. erythraea which has positive influence on erythromycin yield. Like bldD, SACE_5599 is involved in morphological development of S. erythraea, suggesting a very close relationship between secondary metabolite biosynthesis and morphological differentiation in this organism. While the mode of action of SACE_5599 remains to be elucidated, the manipulation of this gene clearly shows potential for improvement of erythromycin production in S. erythraea in industrial setting. We have also demonstrated the applicability of the comparative proteomics approach for identifying new regulatory elements involved in biosynthesis of secondary metabolites in industrial conditions.</description><identifier>ISSN: 1475-2859</identifier><identifier>EISSN: 1475-2859</identifier><identifier>DOI: 10.1186/1475-2859-12-126</identifier><identifier>PMID: 24341557</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Actinomycetes ; Analysis ; Bacterial Proteins - genetics ; Bacterial Proteins - metabolism ; Binding sites ; Biology ; Biosynthesis ; Data processing ; Erythromycin ; Erythromycin - biosynthesis ; Erythromycin - metabolism ; Fermentation ; Genes ; Genetic aspects ; Genetic Engineering ; Metabolites ; Methods ; Microbiology ; Morphological diversity ; Natural products ; Physiological aspects ; Proteins ; Saccharomyces ; Saccharopolyspora - genetics ; Saccharopolyspora - growth & development ; Saccharopolyspora - metabolism ; Statistical analysis ; Studies</subject><ispartof>Microbial cell factories, 2013-12, Vol.12 (1), p.126-126, Article 126</ispartof><rights>COPYRIGHT 2013 BioMed Central Ltd.</rights><rights>2013 Kirm et al.; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.</rights><rights>Copyright © 2013 Kirm et al.; licensee BioMed Central Ltd. 2013 Kirm et al.; licensee BioMed Central Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c558t-da3910184c479c3a713e1ac427310d798db602a46da28261aff009230743c3473</citedby><cites>FETCH-LOGICAL-c558t-da3910184c479c3a713e1ac427310d798db602a46da28261aff009230743c3473</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3878487/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3878487/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,724,777,781,861,882,27905,27906,53772,53774</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24341557$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kirm, Benjamin</creatorcontrib><creatorcontrib>Magdevska, Vasilka</creatorcontrib><creatorcontrib>Tome, Miha</creatorcontrib><creatorcontrib>Horvat, Marinka</creatorcontrib><creatorcontrib>Karničar, Katarina</creatorcontrib><creatorcontrib>Petek, Marko</creatorcontrib><creatorcontrib>Vidmar, Robert</creatorcontrib><creatorcontrib>Baebler, Spela</creatorcontrib><creatorcontrib>Jamnik, Polona</creatorcontrib><creatorcontrib>Fujs, Štefan</creatorcontrib><creatorcontrib>Horvat, Jaka</creatorcontrib><creatorcontrib>Fonovič, Marko</creatorcontrib><creatorcontrib>Turk, Boris</creatorcontrib><creatorcontrib>Gruden, Kristina</creatorcontrib><creatorcontrib>Petković, Hrvoje</creatorcontrib><creatorcontrib>Kosec, Gregor</creatorcontrib><title>SACE_5599, a putative regulatory protein, is involved in morphological differentiation and erythromycin production in Saccharopolyspora erythraea</title><title>Microbial cell factories</title><addtitle>Microb Cell Fact</addtitle><description>Erythromycin is a medically important antibiotic, biosynthesized by the actinomycete Saccharopolyspora erythraea. Genes encoding erythromycin biosynthesis are organized in a gene cluster, spanning over 60 kbp of DNA. Most often, gene clusters encoding biosynthesis of secondary metabolites contain regulatory genes. In contrast, the erythromycin gene cluster does not contain regulatory genes and regulation of its biosynthesis has therefore remained poorly understood, which has for a long time limited genetic engineering approaches for erythromycin yield improvement.
We used a comparative proteomic approach to screen for potential regulatory proteins involved in erythromycin biosynthesis. We have identified a putative regulatory protein SACE_5599 which shows significantly higher levels of expression in an erythromycin high-producing strain, compared to the wild type S. erythraea strain. SACE_5599 is a member of an uncharacterized family of putative regulatory genes, located in several actinomycete biosynthetic gene clusters. Importantly, increased expression of SACE_5599 was observed in the complex fermentation medium and at controlled bioprocess conditions, simulating a high-yield industrial fermentation process in the bioreactor. Inactivation of SACE_5599 in the high-producing strain significantly reduced erythromycin yield, in addition to drastically decreasing sporulation intensity of the SACE_5599-inactivated strains when cultivated on ABSM4 agar medium. In contrast, constitutive overexpression of SACE_5599 in the wild type NRRL23338 strain resulted in an increase of erythromycin yield by 32%. Similar yield increase was also observed when we overexpressed the bldD gene, a previously identified regulator of erythromycin biosynthesis, thereby for the first time revealing its potential for improving erythromycin biosynthesis.
SACE_5599 is the second putative regulatory gene to be identified in S. erythraea which has positive influence on erythromycin yield. Like bldD, SACE_5599 is involved in morphological development of S. erythraea, suggesting a very close relationship between secondary metabolite biosynthesis and morphological differentiation in this organism. While the mode of action of SACE_5599 remains to be elucidated, the manipulation of this gene clearly shows potential for improvement of erythromycin production in S. erythraea in industrial setting. We have also demonstrated the applicability of the comparative proteomics approach for identifying new regulatory elements involved in biosynthesis of secondary metabolites in industrial conditions.</description><subject>Actinomycetes</subject><subject>Analysis</subject><subject>Bacterial Proteins - genetics</subject><subject>Bacterial Proteins - metabolism</subject><subject>Binding sites</subject><subject>Biology</subject><subject>Biosynthesis</subject><subject>Data processing</subject><subject>Erythromycin</subject><subject>Erythromycin - biosynthesis</subject><subject>Erythromycin - metabolism</subject><subject>Fermentation</subject><subject>Genes</subject><subject>Genetic aspects</subject><subject>Genetic Engineering</subject><subject>Metabolites</subject><subject>Methods</subject><subject>Microbiology</subject><subject>Morphological diversity</subject><subject>Natural products</subject><subject>Physiological aspects</subject><subject>Proteins</subject><subject>Saccharomyces</subject><subject>Saccharopolyspora - genetics</subject><subject>Saccharopolyspora - growth & development</subject><subject>Saccharopolyspora - metabolism</subject><subject>Statistical analysis</subject><subject>Studies</subject><issn>1475-2859</issn><issn>1475-2859</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqNkt-L1DAQx4so3nn67pMUfFG4nvmd9OVgWU49OBBcfQ5zadrN0TY1aRf7Z_gfm3rreis-SAYymXzmy5dhsuwlRhcYK_EOM8kLonhZYJJCPMpOD6XHD_KT7FmMdwhhqSR9mp0QRhnmXJ5mPzar9ZXmvCzPc8iHaYTR7WwebDO1MPow50Pwo3X9ee5i7vqdb3e2Skne-TBsfesbZ6DNK1fXNth-dEnA9zn0VW7DPG6D72aT8CRTTebXX3ptwJgtBD_4do6DD7CHwcLz7EkNbbQv9vdZ9vX91Zf1x-Lm04fr9eqmMJyrsaiAlhhhxQyTpaEgMbUYDCOSYlTJUlW3AhFgogKiiMBQ1wiVhCLJqKFM0rPs8l53mG47W5nkPUCrh-A6CLP24PTxT--2uvE7TZVUTC0Cb_YCwX-bbBx156KxbQu99VPUmJVEkDRn_D8okgu6qL7-C73zU-jTJBIliRJICPGHaqC12vW1TxbNIqpXnDLBsZI8URf_oNKpbOeM723tUv2o4e1RQ2JG-31sYIpRX28-H7PonjXBxxhsfRgdRnrZzsUv18v6aUxSLK5fPRz5oeH3OtKfkqbfIA</recordid><startdate>20131217</startdate><enddate>20131217</enddate><creator>Kirm, Benjamin</creator><creator>Magdevska, Vasilka</creator><creator>Tome, Miha</creator><creator>Horvat, Marinka</creator><creator>Karničar, Katarina</creator><creator>Petek, Marko</creator><creator>Vidmar, Robert</creator><creator>Baebler, Spela</creator><creator>Jamnik, Polona</creator><creator>Fujs, Štefan</creator><creator>Horvat, Jaka</creator><creator>Fonovič, Marko</creator><creator>Turk, Boris</creator><creator>Gruden, Kristina</creator><creator>Petković, Hrvoje</creator><creator>Kosec, Gregor</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><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>ISR</scope><scope>3V.</scope><scope>7QL</scope><scope>7T7</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>P64</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>7QO</scope><scope>5PM</scope></search><sort><creationdate>20131217</creationdate><title>SACE_5599, a putative regulatory protein, is involved in morphological differentiation and erythromycin production in Saccharopolyspora erythraea</title><author>Kirm, Benjamin ; Magdevska, Vasilka ; Tome, Miha ; Horvat, Marinka ; Karničar, Katarina ; Petek, Marko ; Vidmar, Robert ; Baebler, Spela ; Jamnik, Polona ; Fujs, Štefan ; Horvat, Jaka ; Fonovič, Marko ; Turk, Boris ; Gruden, Kristina ; Petković, Hrvoje ; Kosec, Gregor</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c558t-da3910184c479c3a713e1ac427310d798db602a46da28261aff009230743c3473</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Actinomycetes</topic><topic>Analysis</topic><topic>Bacterial Proteins - genetics</topic><topic>Bacterial Proteins - metabolism</topic><topic>Binding sites</topic><topic>Biology</topic><topic>Biosynthesis</topic><topic>Data processing</topic><topic>Erythromycin</topic><topic>Erythromycin - biosynthesis</topic><topic>Erythromycin - metabolism</topic><topic>Fermentation</topic><topic>Genes</topic><topic>Genetic aspects</topic><topic>Genetic Engineering</topic><topic>Metabolites</topic><topic>Methods</topic><topic>Microbiology</topic><topic>Morphological diversity</topic><topic>Natural products</topic><topic>Physiological aspects</topic><topic>Proteins</topic><topic>Saccharomyces</topic><topic>Saccharopolyspora - genetics</topic><topic>Saccharopolyspora - growth & development</topic><topic>Saccharopolyspora - metabolism</topic><topic>Statistical analysis</topic><topic>Studies</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kirm, Benjamin</creatorcontrib><creatorcontrib>Magdevska, Vasilka</creatorcontrib><creatorcontrib>Tome, Miha</creatorcontrib><creatorcontrib>Horvat, Marinka</creatorcontrib><creatorcontrib>Karničar, Katarina</creatorcontrib><creatorcontrib>Petek, Marko</creatorcontrib><creatorcontrib>Vidmar, Robert</creatorcontrib><creatorcontrib>Baebler, Spela</creatorcontrib><creatorcontrib>Jamnik, Polona</creatorcontrib><creatorcontrib>Fujs, Štefan</creatorcontrib><creatorcontrib>Horvat, Jaka</creatorcontrib><creatorcontrib>Fonovič, Marko</creatorcontrib><creatorcontrib>Turk, Boris</creatorcontrib><creatorcontrib>Gruden, Kristina</creatorcontrib><creatorcontrib>Petković, Hrvoje</creatorcontrib><creatorcontrib>Kosec, Gregor</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>Biotechnology Research Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Microbial cell factories</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kirm, Benjamin</au><au>Magdevska, Vasilka</au><au>Tome, Miha</au><au>Horvat, Marinka</au><au>Karničar, Katarina</au><au>Petek, Marko</au><au>Vidmar, Robert</au><au>Baebler, Spela</au><au>Jamnik, Polona</au><au>Fujs, Štefan</au><au>Horvat, Jaka</au><au>Fonovič, Marko</au><au>Turk, Boris</au><au>Gruden, Kristina</au><au>Petković, Hrvoje</au><au>Kosec, Gregor</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>SACE_5599, a putative regulatory protein, is involved in morphological differentiation and erythromycin production in Saccharopolyspora erythraea</atitle><jtitle>Microbial cell factories</jtitle><addtitle>Microb Cell Fact</addtitle><date>2013-12-17</date><risdate>2013</risdate><volume>12</volume><issue>1</issue><spage>126</spage><epage>126</epage><pages>126-126</pages><artnum>126</artnum><issn>1475-2859</issn><eissn>1475-2859</eissn><abstract>Erythromycin is a medically important antibiotic, biosynthesized by the actinomycete Saccharopolyspora erythraea. Genes encoding erythromycin biosynthesis are organized in a gene cluster, spanning over 60 kbp of DNA. Most often, gene clusters encoding biosynthesis of secondary metabolites contain regulatory genes. In contrast, the erythromycin gene cluster does not contain regulatory genes and regulation of its biosynthesis has therefore remained poorly understood, which has for a long time limited genetic engineering approaches for erythromycin yield improvement.
We used a comparative proteomic approach to screen for potential regulatory proteins involved in erythromycin biosynthesis. We have identified a putative regulatory protein SACE_5599 which shows significantly higher levels of expression in an erythromycin high-producing strain, compared to the wild type S. erythraea strain. SACE_5599 is a member of an uncharacterized family of putative regulatory genes, located in several actinomycete biosynthetic gene clusters. Importantly, increased expression of SACE_5599 was observed in the complex fermentation medium and at controlled bioprocess conditions, simulating a high-yield industrial fermentation process in the bioreactor. Inactivation of SACE_5599 in the high-producing strain significantly reduced erythromycin yield, in addition to drastically decreasing sporulation intensity of the SACE_5599-inactivated strains when cultivated on ABSM4 agar medium. In contrast, constitutive overexpression of SACE_5599 in the wild type NRRL23338 strain resulted in an increase of erythromycin yield by 32%. Similar yield increase was also observed when we overexpressed the bldD gene, a previously identified regulator of erythromycin biosynthesis, thereby for the first time revealing its potential for improving erythromycin biosynthesis.
SACE_5599 is the second putative regulatory gene to be identified in S. erythraea which has positive influence on erythromycin yield. Like bldD, SACE_5599 is involved in morphological development of S. erythraea, suggesting a very close relationship between secondary metabolite biosynthesis and morphological differentiation in this organism. While the mode of action of SACE_5599 remains to be elucidated, the manipulation of this gene clearly shows potential for improvement of erythromycin production in S. erythraea in industrial setting. We have also demonstrated the applicability of the comparative proteomics approach for identifying new regulatory elements involved in biosynthesis of secondary metabolites in industrial conditions.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>24341557</pmid><doi>10.1186/1475-2859-12-126</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Actinomycetes Analysis Bacterial Proteins - genetics Bacterial Proteins - metabolism Binding sites Biology Biosynthesis Data processing Erythromycin Erythromycin - biosynthesis Erythromycin - metabolism Fermentation Genes Genetic aspects Genetic Engineering Metabolites Methods Microbiology Morphological diversity Natural products Physiological aspects Proteins Saccharomyces Saccharopolyspora - genetics Saccharopolyspora - growth & development Saccharopolyspora - metabolism Statistical analysis Studies |
title | SACE_5599, a putative regulatory protein, is involved in morphological differentiation and erythromycin production in Saccharopolyspora erythraea |
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