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Identification and heterologous expression of the globomycin biosynthetic gene cluster
Globomycin is a cyclic lipodepsipeptide originally isolated from several Streptomyces species which displays strong and selective antibacterial activity against Gram-negative pathogens. Its mode of action is based on the competitive inhibition of the lipoprotein signal peptidase II (LspA), which is...
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Published in: | Synthetic and systems biotechnology 2023-06, Vol.8 (2), p.206-212 |
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creator | Oves-Costales, Daniel Gren, Tetiana Sterndorff, Eva Baggesgaard Martín, Jesús Ortiz-López, Francisco Javier Jørgensen, Tue S. Jiang, Xinglin Román-Hurtado, Fernando Reyes, Fernando Genilloud, Olga Weber, Tilmann |
description | Globomycin is a cyclic lipodepsipeptide originally isolated from several Streptomyces species which displays strong and selective antibacterial activity against Gram-negative pathogens. Its mode of action is based on the competitive inhibition of the lipoprotein signal peptidase II (LspA), which is absent in eukaryotes and considered an attractive target for the development of new antibiotics. Despite its interesting biological properties, the gene cluster encoding its biosynthesis has not yet been identified. In this study we employed a genome-mining approach in the globomycin-producing Streptomyces sp. CA-278952 to identify a candidate gene cluster responsible for its biosynthesis. A null mutant was constructed using CRISPR base editing where production was abolished, strongly suggesting its involvement in the biosynthesis. The putative gene cluster was then cloned and heterologously expressed in Streptomyces albus J1074 and Streptomyces coelicolor M1146, therefore unambiguously linking globomycin and its biosynthetic gene cluster. Our work paves the way for the biosynthesis of new globomycin derivatives with improved pharmacological properties.
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doi_str_mv | 10.1016/j.synbio.2023.02.001 |
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[Display omitted]</description><identifier>ISSN: 2405-805X</identifier><identifier>EISSN: 2405-805X</identifier><identifier>DOI: 10.1016/j.synbio.2023.02.001</identifier><identifier>PMID: 36844473</identifier><language>eng</language><publisher>China: Elsevier B.V</publisher><subject>CRISPR-cBEST ; Cyclic lipodepsipeptide ; Genome mining ; Globomycin ; Heterologous expression ; Original ; Signal peptidase II</subject><ispartof>Synthetic and systems biotechnology, 2023-06, Vol.8 (2), p.206-212</ispartof><rights>2023 The Authors</rights><rights>2023 The Authors.</rights><rights>2023 The Authors 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c529t-aad34bd97ee375db6352a410aa273dceb3526ffdf7d447bb688d92d4a091cbe3</citedby><cites>FETCH-LOGICAL-c529t-aad34bd97ee375db6352a410aa273dceb3526ffdf7d447bb688d92d4a091cbe3</cites><orcidid>0000-0002-4935-8025 ; 0000-0002-8260-5120 ; 0000-0001-9986-4623 ; 0000-0003-1607-5106 ; 0000-0003-2517-9978</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9943842/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S2405805X23000066$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,3536,27901,27902,45756,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36844473$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Oves-Costales, Daniel</creatorcontrib><creatorcontrib>Gren, Tetiana</creatorcontrib><creatorcontrib>Sterndorff, Eva Baggesgaard</creatorcontrib><creatorcontrib>Martín, Jesús</creatorcontrib><creatorcontrib>Ortiz-López, Francisco Javier</creatorcontrib><creatorcontrib>Jørgensen, Tue S.</creatorcontrib><creatorcontrib>Jiang, Xinglin</creatorcontrib><creatorcontrib>Román-Hurtado, Fernando</creatorcontrib><creatorcontrib>Reyes, Fernando</creatorcontrib><creatorcontrib>Genilloud, Olga</creatorcontrib><creatorcontrib>Weber, Tilmann</creatorcontrib><title>Identification and heterologous expression of the globomycin biosynthetic gene cluster</title><title>Synthetic and systems biotechnology</title><addtitle>Synth Syst Biotechnol</addtitle><description>Globomycin is a cyclic lipodepsipeptide originally isolated from several Streptomyces species which displays strong and selective antibacterial activity against Gram-negative pathogens. Its mode of action is based on the competitive inhibition of the lipoprotein signal peptidase II (LspA), which is absent in eukaryotes and considered an attractive target for the development of new antibiotics. Despite its interesting biological properties, the gene cluster encoding its biosynthesis has not yet been identified. In this study we employed a genome-mining approach in the globomycin-producing Streptomyces sp. CA-278952 to identify a candidate gene cluster responsible for its biosynthesis. A null mutant was constructed using CRISPR base editing where production was abolished, strongly suggesting its involvement in the biosynthesis. The putative gene cluster was then cloned and heterologously expressed in Streptomyces albus J1074 and Streptomyces coelicolor M1146, therefore unambiguously linking globomycin and its biosynthetic gene cluster. Our work paves the way for the biosynthesis of new globomycin derivatives with improved pharmacological properties.
[Display omitted]</description><subject>CRISPR-cBEST</subject><subject>Cyclic lipodepsipeptide</subject><subject>Genome mining</subject><subject>Globomycin</subject><subject>Heterologous expression</subject><subject>Original</subject><subject>Signal peptidase II</subject><issn>2405-805X</issn><issn>2405-805X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNp9UUtP3DAQjqqigoB_UFU59rLBrzjOpVKF2rISUi-o6s3yY5L1Kmtv7Szq_ntmWaBw6cn2zHwPz1dVHylpKKHyat2UfbQhNYww3hDWEELfVWdMkHahSPv7_av7aXVZyprghGJS9upDdcqlEkJ0_Kz6tfQQ5zAEZ-aQYm2ir1cwQ05TGtOu1PB3m6GUQy8N9byCepySTZu9C7FGB-gDi3Nw9QgRajftCqIvqpPBTAUun87z6u77t7vrm8Xtzx_L66-3C9eyfl4Y47mwvu8AeNd6K3nLjKDEGNZx78DiWw6DHzqPdq2VSvmeeWFIT50Ffl4tj7Q-mbXe5rAxea-TCfqxkPKoTUZvE2hQhLSM2g4JEC9V7xUn0vjeyxaEQa4vR67tzm4AxeOczfSG9G0nhpUe073ue8GVYEjw-Ykgpz87KLPehOJgmkwE3KRmnSJCyY5SHBXHUZdTKRmGFxlK9CFgvdbHgPUhYE2YxvgQ9um1xRfQc5z__gC48_sAWRcXIDrwIYObcSvh_woPd768NA</recordid><startdate>20230601</startdate><enddate>20230601</enddate><creator>Oves-Costales, Daniel</creator><creator>Gren, Tetiana</creator><creator>Sterndorff, Eva Baggesgaard</creator><creator>Martín, Jesús</creator><creator>Ortiz-López, Francisco Javier</creator><creator>Jørgensen, Tue S.</creator><creator>Jiang, Xinglin</creator><creator>Román-Hurtado, Fernando</creator><creator>Reyes, Fernando</creator><creator>Genilloud, Olga</creator><creator>Weber, Tilmann</creator><general>Elsevier B.V</general><general>KeAi Publishing</general><general>KeAi Communications Co., Ltd</general><scope>6I.</scope><scope>AAFTH</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-4935-8025</orcidid><orcidid>https://orcid.org/0000-0002-8260-5120</orcidid><orcidid>https://orcid.org/0000-0001-9986-4623</orcidid><orcidid>https://orcid.org/0000-0003-1607-5106</orcidid><orcidid>https://orcid.org/0000-0003-2517-9978</orcidid></search><sort><creationdate>20230601</creationdate><title>Identification and heterologous expression of the globomycin biosynthetic gene cluster</title><author>Oves-Costales, Daniel ; 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Its mode of action is based on the competitive inhibition of the lipoprotein signal peptidase II (LspA), which is absent in eukaryotes and considered an attractive target for the development of new antibiotics. Despite its interesting biological properties, the gene cluster encoding its biosynthesis has not yet been identified. In this study we employed a genome-mining approach in the globomycin-producing Streptomyces sp. CA-278952 to identify a candidate gene cluster responsible for its biosynthesis. A null mutant was constructed using CRISPR base editing where production was abolished, strongly suggesting its involvement in the biosynthesis. The putative gene cluster was then cloned and heterologously expressed in Streptomyces albus J1074 and Streptomyces coelicolor M1146, therefore unambiguously linking globomycin and its biosynthetic gene cluster. Our work paves the way for the biosynthesis of new globomycin derivatives with improved pharmacological properties.
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subjects | CRISPR-cBEST Cyclic lipodepsipeptide Genome mining Globomycin Heterologous expression Original Signal peptidase II |
title | Identification and heterologous expression of the globomycin biosynthetic gene cluster |
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