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Cloning, reassembling and integration of the entire nikkomycin biosynthetic gene cluster into Streptomyces ansochromogenes lead to an improved nikkomycin production

BACKGROUND: Nikkomycins are a group of peptidyl nucleoside antibiotics produced by Streptomyces ansochromogenes. They are competitive inhibitors of chitin synthase and show potent fungicidal, insecticidal, and acaricidal activities. Nikkomycin X and Z are the main components produced by S. ansochrom...

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Autores principales: Liao, Guojian, Li, Jine, Li, Lei, Yang, Haihua, Tian, Yuqing, Tan, Huarong
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2817672/
https://www.ncbi.nlm.nih.gov/pubmed/20096125
http://dx.doi.org/10.1186/1475-2859-9-6
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author Liao, Guojian
Li, Jine
Li, Lei
Yang, Haihua
Tian, Yuqing
Tan, Huarong
author_facet Liao, Guojian
Li, Jine
Li, Lei
Yang, Haihua
Tian, Yuqing
Tan, Huarong
author_sort Liao, Guojian
collection PubMed
description BACKGROUND: Nikkomycins are a group of peptidyl nucleoside antibiotics produced by Streptomyces ansochromogenes. They are competitive inhibitors of chitin synthase and show potent fungicidal, insecticidal, and acaricidal activities. Nikkomycin X and Z are the main components produced by S. ansochromogenes. Generation of a high-producing strain is crucial to scale up nikkomycins production for further clinical trials. RESULTS: To increase the yields of nikkomycins, an additional copy of nikkomycin biosynthetic gene cluster (35 kb) was introduced into nikkomycin producing strain, S. ansochromogenes 7100. The gene cluster was first reassembled into an integrative plasmid by Red/ET technology combining with classic cloning methods and then the resulting plasmid(pNIK)was introduced into S. ansochromogenes by conjugal transfer. Introduction of pNIK led to enhanced production of nikkomycins (880 mg L(-1), 4 -fold nikkomycin X and 210 mg L(-1), 1.8-fold nikkomycin Z) in the resulting exconjugants comparing with the parent strain (220 mg L(-1 )nikkomycin X and 120 mg L(-1 )nikkomycin Z). The exconjugants are genetically stable in the absence of antibiotic resistance selection pressure. CONCLUSION: A high nikkomycins producing strain (1100 mg L(-1 )nikkomycins) was obtained by introduction of an extra nikkomycin biosynthetic gene cluster into the genome of S. ansochromogenes. The strategies presented here could be applicable to other bacteria to improve the yields of secondary metabolites.
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spelling pubmed-28176722010-02-09 Cloning, reassembling and integration of the entire nikkomycin biosynthetic gene cluster into Streptomyces ansochromogenes lead to an improved nikkomycin production Liao, Guojian Li, Jine Li, Lei Yang, Haihua Tian, Yuqing Tan, Huarong Microb Cell Fact Research BACKGROUND: Nikkomycins are a group of peptidyl nucleoside antibiotics produced by Streptomyces ansochromogenes. They are competitive inhibitors of chitin synthase and show potent fungicidal, insecticidal, and acaricidal activities. Nikkomycin X and Z are the main components produced by S. ansochromogenes. Generation of a high-producing strain is crucial to scale up nikkomycins production for further clinical trials. RESULTS: To increase the yields of nikkomycins, an additional copy of nikkomycin biosynthetic gene cluster (35 kb) was introduced into nikkomycin producing strain, S. ansochromogenes 7100. The gene cluster was first reassembled into an integrative plasmid by Red/ET technology combining with classic cloning methods and then the resulting plasmid(pNIK)was introduced into S. ansochromogenes by conjugal transfer. Introduction of pNIK led to enhanced production of nikkomycins (880 mg L(-1), 4 -fold nikkomycin X and 210 mg L(-1), 1.8-fold nikkomycin Z) in the resulting exconjugants comparing with the parent strain (220 mg L(-1 )nikkomycin X and 120 mg L(-1 )nikkomycin Z). The exconjugants are genetically stable in the absence of antibiotic resistance selection pressure. CONCLUSION: A high nikkomycins producing strain (1100 mg L(-1 )nikkomycins) was obtained by introduction of an extra nikkomycin biosynthetic gene cluster into the genome of S. ansochromogenes. The strategies presented here could be applicable to other bacteria to improve the yields of secondary metabolites. BioMed Central 2010-01-23 /pmc/articles/PMC2817672/ /pubmed/20096125 http://dx.doi.org/10.1186/1475-2859-9-6 Text en Copyright ©2010 Liao et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 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.
spellingShingle Research
Liao, Guojian
Li, Jine
Li, Lei
Yang, Haihua
Tian, Yuqing
Tan, Huarong
Cloning, reassembling and integration of the entire nikkomycin biosynthetic gene cluster into Streptomyces ansochromogenes lead to an improved nikkomycin production
title Cloning, reassembling and integration of the entire nikkomycin biosynthetic gene cluster into Streptomyces ansochromogenes lead to an improved nikkomycin production
title_full Cloning, reassembling and integration of the entire nikkomycin biosynthetic gene cluster into Streptomyces ansochromogenes lead to an improved nikkomycin production
title_fullStr Cloning, reassembling and integration of the entire nikkomycin biosynthetic gene cluster into Streptomyces ansochromogenes lead to an improved nikkomycin production
title_full_unstemmed Cloning, reassembling and integration of the entire nikkomycin biosynthetic gene cluster into Streptomyces ansochromogenes lead to an improved nikkomycin production
title_short Cloning, reassembling and integration of the entire nikkomycin biosynthetic gene cluster into Streptomyces ansochromogenes lead to an improved nikkomycin production
title_sort cloning, reassembling and integration of the entire nikkomycin biosynthetic gene cluster into streptomyces ansochromogenes lead to an improved nikkomycin production
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2817672/
https://www.ncbi.nlm.nih.gov/pubmed/20096125
http://dx.doi.org/10.1186/1475-2859-9-6
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