Isolation of two new stereochemical variants of streptophenazine by cocultivation of Streptomyces NIIST-D31, Streptomyces NIIST-D47, and Streptomyces NIIST-D63 strains in 3C2 combinations
Cocultivation of combinations of Streptomyces species isolated from the same soil was explored to isolate novel secondary metabolites. Recently, we reported the isolation of a novel vicinal diepoxide of alloaureothin along with three carboxamides, 4-aminobenzoic acid, and 1,6-dimethoxyphenazine from...
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creator | Induja, D. K. Jesmina, A. R. S. Joseph, Manu M. Shamjith, Shanmughan Ingaladal, Nagaraja Maiti, Kaustabh Kumar Kumar, B. S. Dileep Lankalapalli, Ravi S. |
description | Cocultivation of combinations of
Streptomyces
species isolated from the same soil was explored to isolate novel secondary metabolites. Recently, we reported the isolation of a novel vicinal diepoxide of alloaureothin along with three carboxamides, 4-aminobenzoic acid, and 1,6-dimethoxyphenazine from the individual culture of
Streptomyces luteireticuli
NIIST-D31. Herein, cocultivation of NIIST-D31 with
Streptomyces luteoverticillatus
NIIST-D47 afforded two new stereochemical variants of streptophenazine (S1 and S2), and 1-
N
-methylalbonoursin, where the individual culture of NIIST-D47 primarily produced carbazomycins A, D, and E. The new streptophenazines and 1-
N
-methylalbonoursin were also observed during cocultivation of NIIST-D31 with
Streptomyces thioluteus
NIIST-D63, where the individual culture of NIIST-D63 strain afforded for the first time 2,2′-bipyridines (caerulomycinamide and dipyrimicin B), picolinamide, 2,3-dimethoxybenzamide, 2-hydroxy-3-methoxybenzamide, and 6-amino-2-pyridone along with known natural products aureothin and 1,6-dimethoxyphenazine. Finally, cocultivation of NIIST-D47 and NIIST-D63 strains produced carbazomycins B and C, alloaureothin, cyclo-(Leu-Pro), investiamide, and 4-aminobenzoic acid. Some of the compounds observed in the individual cultures were also produced in cocultivations. Improvement in the yield of secondary metabolites during cocultivation compared to individual culturing is well-known, which is noted here for vicinal diepoxide of alloaureothin. The production of new streptophenazines by cocultivation combinations with NIIST-D31 suggests that NIIST-D47 and NIIST-D63 may function as inducers in activating cryptic secondary metabolite-biosynthetic gene clusters. Cytotoxicity of the new streptophenazines in cancerous (MCF7 and MDA-MB-231) or non-cancerous (WI-38) cells were tested, however, they exhibited no significant activity. |
doi_str_mv | 10.1038/s41429-023-00638-7 |
format | Article |
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Streptomyces
species isolated from the same soil was explored to isolate novel secondary metabolites. Recently, we reported the isolation of a novel vicinal diepoxide of alloaureothin along with three carboxamides, 4-aminobenzoic acid, and 1,6-dimethoxyphenazine from the individual culture of
Streptomyces luteireticuli
NIIST-D31. Herein, cocultivation of NIIST-D31 with
Streptomyces luteoverticillatus
NIIST-D47 afforded two new stereochemical variants of streptophenazine (S1 and S2), and 1-
N
-methylalbonoursin, where the individual culture of NIIST-D47 primarily produced carbazomycins A, D, and E. The new streptophenazines and 1-
N
-methylalbonoursin were also observed during cocultivation of NIIST-D31 with
Streptomyces thioluteus
NIIST-D63, where the individual culture of NIIST-D63 strain afforded for the first time 2,2′-bipyridines (caerulomycinamide and dipyrimicin B), picolinamide, 2,3-dimethoxybenzamide, 2-hydroxy-3-methoxybenzamide, and 6-amino-2-pyridone along with known natural products aureothin and 1,6-dimethoxyphenazine. Finally, cocultivation of NIIST-D47 and NIIST-D63 strains produced carbazomycins B and C, alloaureothin, cyclo-(Leu-Pro), investiamide, and 4-aminobenzoic acid. Some of the compounds observed in the individual cultures were also produced in cocultivations. Improvement in the yield of secondary metabolites during cocultivation compared to individual culturing is well-known, which is noted here for vicinal diepoxide of alloaureothin. The production of new streptophenazines by cocultivation combinations with NIIST-D31 suggests that NIIST-D47 and NIIST-D63 may function as inducers in activating cryptic secondary metabolite-biosynthetic gene clusters. Cytotoxicity of the new streptophenazines in cancerous (MCF7 and MDA-MB-231) or non-cancerous (WI-38) cells were tested, however, they exhibited no significant activity.</description><identifier>ISSN: 0021-8820</identifier><identifier>ISSN: 1881-1469</identifier><identifier>EISSN: 1881-1469</identifier><identifier>DOI: 10.1038/s41429-023-00638-7</identifier><language>eng</language><publisher>Tokyo: Springer Japan</publisher><subject>631/326 ; 639/638 ; Bacteriology ; Biomedical and Life Sciences ; Bioorganic Chemistry ; Cell culture ; Cytotoxicity ; Gene clusters ; Life Sciences ; Medicinal Chemistry ; Metabolites ; Microbiology ; Natural products ; Organic Chemistry ; para-Aminobenzoic acid ; Secondary metabolites ; Streptomyces</subject><ispartof>Journal of antibiotics, 2023-10, Vol.76 (10), p.567-578</ispartof><rights>The Author(s), under exclusive licence to the Japan Antibiotics Research Association 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.</rights><rights>2023. The Author(s), under exclusive licence to the Japan Antibiotics Research Association.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c306t-88e78d9780121f67c2bd7620a46d25e4ef2f38d2b6cd5c4a38a8a8f04931256f3</citedby><cites>FETCH-LOGICAL-c306t-88e78d9780121f67c2bd7620a46d25e4ef2f38d2b6cd5c4a38a8a8f04931256f3</cites><orcidid>0000-0001-8223-7674</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Induja, D. K.</creatorcontrib><creatorcontrib>Jesmina, A. R. S.</creatorcontrib><creatorcontrib>Joseph, Manu M.</creatorcontrib><creatorcontrib>Shamjith, Shanmughan</creatorcontrib><creatorcontrib>Ingaladal, Nagaraja</creatorcontrib><creatorcontrib>Maiti, Kaustabh Kumar</creatorcontrib><creatorcontrib>Kumar, B. S. Dileep</creatorcontrib><creatorcontrib>Lankalapalli, Ravi S.</creatorcontrib><title>Isolation of two new stereochemical variants of streptophenazine by cocultivation of Streptomyces NIIST-D31, Streptomyces NIIST-D47, and Streptomyces NIIST-D63 strains in 3C2 combinations</title><title>Journal of antibiotics</title><addtitle>J Antibiot</addtitle><description>Cocultivation of combinations of
Streptomyces
species isolated from the same soil was explored to isolate novel secondary metabolites. Recently, we reported the isolation of a novel vicinal diepoxide of alloaureothin along with three carboxamides, 4-aminobenzoic acid, and 1,6-dimethoxyphenazine from the individual culture of
Streptomyces luteireticuli
NIIST-D31. Herein, cocultivation of NIIST-D31 with
Streptomyces luteoverticillatus
NIIST-D47 afforded two new stereochemical variants of streptophenazine (S1 and S2), and 1-
N
-methylalbonoursin, where the individual culture of NIIST-D47 primarily produced carbazomycins A, D, and E. The new streptophenazines and 1-
N
-methylalbonoursin were also observed during cocultivation of NIIST-D31 with
Streptomyces thioluteus
NIIST-D63, where the individual culture of NIIST-D63 strain afforded for the first time 2,2′-bipyridines (caerulomycinamide and dipyrimicin B), picolinamide, 2,3-dimethoxybenzamide, 2-hydroxy-3-methoxybenzamide, and 6-amino-2-pyridone along with known natural products aureothin and 1,6-dimethoxyphenazine. Finally, cocultivation of NIIST-D47 and NIIST-D63 strains produced carbazomycins B and C, alloaureothin, cyclo-(Leu-Pro), investiamide, and 4-aminobenzoic acid. Some of the compounds observed in the individual cultures were also produced in cocultivations. Improvement in the yield of secondary metabolites during cocultivation compared to individual culturing is well-known, which is noted here for vicinal diepoxide of alloaureothin. The production of new streptophenazines by cocultivation combinations with NIIST-D31 suggests that NIIST-D47 and NIIST-D63 may function as inducers in activating cryptic secondary metabolite-biosynthetic gene clusters. Cytotoxicity of the new streptophenazines in cancerous (MCF7 and MDA-MB-231) or non-cancerous (WI-38) cells were tested, however, they exhibited no significant activity.</description><subject>631/326</subject><subject>639/638</subject><subject>Bacteriology</subject><subject>Biomedical and Life Sciences</subject><subject>Bioorganic Chemistry</subject><subject>Cell culture</subject><subject>Cytotoxicity</subject><subject>Gene clusters</subject><subject>Life Sciences</subject><subject>Medicinal Chemistry</subject><subject>Metabolites</subject><subject>Microbiology</subject><subject>Natural products</subject><subject>Organic Chemistry</subject><subject>para-Aminobenzoic acid</subject><subject>Secondary metabolites</subject><subject>Streptomyces</subject><issn>0021-8820</issn><issn>1881-1469</issn><issn>1881-1469</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>BENPR</sourceid><recordid>eNp9kV9rFDEUxYMouFa_gE8BX3zoaP7MJJlHWasulPrQ-hyymTs2ZSZZc7Mt61fzyzXbEQUpkocLye-ck8sh5DVn7ziT5j22vBV9w4RsGFPSNPoJWXFjeMNb1T8lK8YEb4wR7Dl5gXjDmNRSmxX5tcE0uRJSpGmk5S7RCHcUC2RI_hrm4N1Eb10OLhY8Ilgy7EraXUN0P0MEuj1Qn_x-KuH2j8_lAs0HD0gvNpvLq-aj5KeP3rf6lLo4PPqm5DHPhYg0RCrXokbN2xAfgvAleTa6CeHV73lCvn06u1p_ac6_ft6sP5w3XjJV6tagzdBrw7jgo9JebAetBHOtGkQHLYxilGYQW-WHzrdOGlfPyNpectGpUZ6Qt4vvLqcfe8Bi54AepslFSHu0woiuY5VXFX3zD3qT9jnW31VK9awTwshKiYXyOSFmGO0uh9nlg-XMHvu0S5-29mkf-rS6iuQiwgrH75D_Wv9HdQ-yzKQk</recordid><startdate>20231001</startdate><enddate>20231001</enddate><creator>Induja, D. 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Dileep</creator><creator>Lankalapalli, Ravi S.</creator><general>Springer Japan</general><general>Nature Publishing Group</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QL</scope><scope>7T5</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</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>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>M2P</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-8223-7674</orcidid></search><sort><creationdate>20231001</creationdate><title>Isolation of two new stereochemical variants of streptophenazine by cocultivation of Streptomyces NIIST-D31, Streptomyces NIIST-D47, and Streptomyces NIIST-D63 strains in 3C2 combinations</title><author>Induja, D. K. ; Jesmina, A. R. S. ; Joseph, Manu M. ; Shamjith, Shanmughan ; Ingaladal, Nagaraja ; Maiti, Kaustabh Kumar ; Kumar, B. S. Dileep ; Lankalapalli, Ravi S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c306t-88e78d9780121f67c2bd7620a46d25e4ef2f38d2b6cd5c4a38a8a8f04931256f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>631/326</topic><topic>639/638</topic><topic>Bacteriology</topic><topic>Biomedical and Life Sciences</topic><topic>Bioorganic Chemistry</topic><topic>Cell culture</topic><topic>Cytotoxicity</topic><topic>Gene clusters</topic><topic>Life Sciences</topic><topic>Medicinal Chemistry</topic><topic>Metabolites</topic><topic>Microbiology</topic><topic>Natural products</topic><topic>Organic Chemistry</topic><topic>para-Aminobenzoic acid</topic><topic>Secondary metabolites</topic><topic>Streptomyces</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Induja, D. K.</creatorcontrib><creatorcontrib>Jesmina, A. R. S.</creatorcontrib><creatorcontrib>Joseph, Manu M.</creatorcontrib><creatorcontrib>Shamjith, Shanmughan</creatorcontrib><creatorcontrib>Ingaladal, Nagaraja</creatorcontrib><creatorcontrib>Maiti, Kaustabh Kumar</creatorcontrib><creatorcontrib>Kumar, B. S. Dileep</creatorcontrib><creatorcontrib>Lankalapalli, Ravi S.</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Immunology Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</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>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>Science Database</collection><collection>Biological Science 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 Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of antibiotics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Induja, D. K.</au><au>Jesmina, A. R. S.</au><au>Joseph, Manu M.</au><au>Shamjith, Shanmughan</au><au>Ingaladal, Nagaraja</au><au>Maiti, Kaustabh Kumar</au><au>Kumar, B. S. Dileep</au><au>Lankalapalli, Ravi S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Isolation of two new stereochemical variants of streptophenazine by cocultivation of Streptomyces NIIST-D31, Streptomyces NIIST-D47, and Streptomyces NIIST-D63 strains in 3C2 combinations</atitle><jtitle>Journal of antibiotics</jtitle><stitle>J Antibiot</stitle><date>2023-10-01</date><risdate>2023</risdate><volume>76</volume><issue>10</issue><spage>567</spage><epage>578</epage><pages>567-578</pages><issn>0021-8820</issn><issn>1881-1469</issn><eissn>1881-1469</eissn><abstract>Cocultivation of combinations of
Streptomyces
species isolated from the same soil was explored to isolate novel secondary metabolites. Recently, we reported the isolation of a novel vicinal diepoxide of alloaureothin along with three carboxamides, 4-aminobenzoic acid, and 1,6-dimethoxyphenazine from the individual culture of
Streptomyces luteireticuli
NIIST-D31. Herein, cocultivation of NIIST-D31 with
Streptomyces luteoverticillatus
NIIST-D47 afforded two new stereochemical variants of streptophenazine (S1 and S2), and 1-
N
-methylalbonoursin, where the individual culture of NIIST-D47 primarily produced carbazomycins A, D, and E. The new streptophenazines and 1-
N
-methylalbonoursin were also observed during cocultivation of NIIST-D31 with
Streptomyces thioluteus
NIIST-D63, where the individual culture of NIIST-D63 strain afforded for the first time 2,2′-bipyridines (caerulomycinamide and dipyrimicin B), picolinamide, 2,3-dimethoxybenzamide, 2-hydroxy-3-methoxybenzamide, and 6-amino-2-pyridone along with known natural products aureothin and 1,6-dimethoxyphenazine. Finally, cocultivation of NIIST-D47 and NIIST-D63 strains produced carbazomycins B and C, alloaureothin, cyclo-(Leu-Pro), investiamide, and 4-aminobenzoic acid. Some of the compounds observed in the individual cultures were also produced in cocultivations. Improvement in the yield of secondary metabolites during cocultivation compared to individual culturing is well-known, which is noted here for vicinal diepoxide of alloaureothin. The production of new streptophenazines by cocultivation combinations with NIIST-D31 suggests that NIIST-D47 and NIIST-D63 may function as inducers in activating cryptic secondary metabolite-biosynthetic gene clusters. Cytotoxicity of the new streptophenazines in cancerous (MCF7 and MDA-MB-231) or non-cancerous (WI-38) cells were tested, however, they exhibited no significant activity.</abstract><cop>Tokyo</cop><pub>Springer Japan</pub><doi>10.1038/s41429-023-00638-7</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0001-8223-7674</orcidid></addata></record> |
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subjects | 631/326 639/638 Bacteriology Biomedical and Life Sciences Bioorganic Chemistry Cell culture Cytotoxicity Gene clusters Life Sciences Medicinal Chemistry Metabolites Microbiology Natural products Organic Chemistry para-Aminobenzoic acid Secondary metabolites Streptomyces |
title | Isolation of two new stereochemical variants of streptophenazine by cocultivation of Streptomyces NIIST-D31, Streptomyces NIIST-D47, and Streptomyces NIIST-D63 strains in 3C2 combinations |
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