Production of microbial secondary metabolites: Regulation by the carbon source

Microbial secondary metabolites are low molecular mass products, not essential for growth of the producing cultures, but very important for human health. They include antibiotics, antitumor agents, cholesterol-lowering drugs, and others. They have unusual structures and are usually formed during the...

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Published inCritical reviews in microbiology Vol. 36; no. 2; pp. 146 - 167
Main Authors Ruiz, Beatriz, Chávez, Adán, Forero, Angela, García-Huante, Yolanda, Romero, Alba, Sánchez, Mauricio, Rocha, Diana, Sánchez, Brenda, Rodríguez-Sanoja, Romina, Sánchez, Sergio, Langley, Elizabeth
Format Journal Article
LanguageEnglish
Published London Informa UK Ltd 01.05.2010
Taylor & Francis
Informa
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Abstract Microbial secondary metabolites are low molecular mass products, not essential for growth of the producing cultures, but very important for human health. They include antibiotics, antitumor agents, cholesterol-lowering drugs, and others. They have unusual structures and are usually formed during the late growth phase of the producing microorganisms. Its synthesis can be influenced greatly by manipulating the type and concentration of the nutrients formulating the culture media. Among these nutrients, the effect of the carbon sources has been the subject of continuous studies for both, industry and research groups. Different mechanisms have been described in bacteria and fungi to explain the negative carbon catabolite effects on secondary metabolite production. Their knowledge and manipulation have been useful either for setting fermentation conditions or for strain improvement. During the last years, important advances have been reported on these mechanisms at the biochemical and molecular levels. The aim of the present review is to describe these advances, giving special emphasis to those reported for the genus Streptomyces.
AbstractList Microbial secondary metabolites are low molecular mass products, not essential for growth of the producing cultures, but very important for human health. They include antibiotics, antitumor agents, cholesterol-lowering drugs, and others. They have unusual structures and are usually formed during the late growth phase of the producing microorganisms. Its synthesis can be influenced greatly by manipulating the type and concentration of the nutrients formulating the culture media. Among these nutrients, the effect of the carbon sources has been the subject of continuous studies for both, industry and research groups. Different mechanisms have been described in bacteria and fungi to explain the negative carbon catabolite effects on secondary metabolite production. Their knowledge and manipulation have been useful either for setting fermentation conditions or for strain improvement. During the last years, important advances have been reported on these mechanisms at the biochemical and molecular levels. The aim of the present review is to describe these advances, giving special emphasis to those reported for the genus Streptomyces.
Microbial secondary metabolites are low molecular mass products, not essential for growth of the producing cultures, but very important for human health. They include antibiotics, antitumor agents, cholesterol-lowering drugs, and others. They have unusual structures and are usually formed during the late growth phase of the producing microorganisms. Its synthesis can be influenced greatly by manipulating the type and concentration of the nutrients formulating the culture media. Among these nutrients, the effect of the carbon sources has been the subject of continuous studies for both, industry and research groups. Different mechanisms have been described in bacteria and fungi to explain the negative carbon catabolite effects on secondary metabolite production. Their knowledge and manipulation have been useful either for setting fermentation conditions or for strain improvement. During the last years, important advances have been reported on these mechanisms at the biochemical and molecular levels. The aim of the present review is to describe these advances, giving special emphasis to those reported for the genus Streptomyces.Microbial secondary metabolites are low molecular mass products, not essential for growth of the producing cultures, but very important for human health. They include antibiotics, antitumor agents, cholesterol-lowering drugs, and others. They have unusual structures and are usually formed during the late growth phase of the producing microorganisms. Its synthesis can be influenced greatly by manipulating the type and concentration of the nutrients formulating the culture media. Among these nutrients, the effect of the carbon sources has been the subject of continuous studies for both, industry and research groups. Different mechanisms have been described in bacteria and fungi to explain the negative carbon catabolite effects on secondary metabolite production. Their knowledge and manipulation have been useful either for setting fermentation conditions or for strain improvement. During the last years, important advances have been reported on these mechanisms at the biochemical and molecular levels. The aim of the present review is to describe these advances, giving special emphasis to those reported for the genus Streptomyces.
Author Langley, Elizabeth
Rodríguez-Sanoja, Romina
Ruiz, Beatriz
Sánchez, Brenda
García-Huante, Yolanda
Romero, Alba
Chávez, Adán
Sánchez, Sergio
Sánchez, Mauricio
Forero, Angela
Rocha, Diana
Author_xml – sequence: 1
  givenname: Beatriz
  surname: Ruiz
  fullname: Ruiz, Beatriz
  email: sersan@biomedicas.unam.mx
  organization: 1Departamento de Biología Molecular y Biotecnología, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, México D.F. 04510. México
– sequence: 2
  givenname: Adán
  surname: Chávez
  fullname: Chávez, Adán
  email: sersan@biomedicas.unam.mx
  organization: 1Departamento de Biología Molecular y Biotecnología, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, México D.F. 04510. México
– sequence: 3
  givenname: Angela
  surname: Forero
  fullname: Forero, Angela
  email: sersan@biomedicas.unam.mx
  organization: 1Departamento de Biología Molecular y Biotecnología, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, México D.F. 04510. México
– sequence: 4
  givenname: Yolanda
  surname: García-Huante
  fullname: García-Huante, Yolanda
  email: sersan@biomedicas.unam.mx
  organization: 1Departamento de Biología Molecular y Biotecnología, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, México D.F. 04510. México
– sequence: 5
  givenname: Alba
  surname: Romero
  fullname: Romero, Alba
  email: sersan@biomedicas.unam.mx
  organization: 1Departamento de Biología Molecular y Biotecnología, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, México D.F. 04510. México
– sequence: 6
  givenname: Mauricio
  surname: Sánchez
  fullname: Sánchez, Mauricio
  email: sersan@biomedicas.unam.mx
  organization: 1Departamento de Biología Molecular y Biotecnología, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, México D.F. 04510. México
– sequence: 7
  givenname: Diana
  surname: Rocha
  fullname: Rocha, Diana
  email: sersan@biomedicas.unam.mx
  organization: 1Departamento de Biología Molecular y Biotecnología, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, México D.F. 04510. México
– sequence: 8
  givenname: Brenda
  surname: Sánchez
  fullname: Sánchez, Brenda
  email: sersan@biomedicas.unam.mx
  organization: 1Departamento de Biología Molecular y Biotecnología, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, México D.F. 04510. México
– sequence: 9
  givenname: Romina
  surname: Rodríguez-Sanoja
  fullname: Rodríguez-Sanoja, Romina
  email: sersan@biomedicas.unam.mx
  organization: 1Departamento de Biología Molecular y Biotecnología, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, México D.F. 04510. México
– sequence: 10
  givenname: Sergio
  surname: Sánchez
  fullname: Sánchez, Sergio
  email: sersan@biomedicas.unam.mx
  organization: 1Departamento de Biología Molecular y Biotecnología, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, México D.F. 04510. México
– sequence: 11
  givenname: Elizabeth
  surname: Langley
  fullname: Langley, Elizabeth
  email: sersan@biomedicas.unam.mx
  organization: 1Departamento de Biología Molecular y Biotecnología, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, México D.F. 04510. México
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Thu Apr 24 23:08:10 EDT 2025
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Issue 2
Keywords catabolite control protein (CCpA)
Carbon source regulation
Streptomycetaceae
Enzyme
Metabolite
strain improvement
Cyclic AMP
Streptomyces
cyclic AMP (cAMP)
Review
Protein
Strain
Actinomycetales
Isomerases
secondary metabolites
Intramolecular transferases
Bacteria
phosphoenolpyruvate:phosphotransferase system (PTS)
Actinomycetes
Bld proteins
Phosphotransferases
carbon catabolite repressor (CreA)
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Snippet Microbial secondary metabolites are low molecular mass products, not essential for growth of the producing cultures, but very important for human health. They...
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SubjectTerms Bacteria - metabolism
Biological and medical sciences
Biological Products - biosynthesis
Biological Products - pharmacology
Bld proteins
carbon
Carbon - metabolism
carbon catabolite repressor (CreA)
Carbon source regulation
catabolite control protein (CCpA)
cyclic AMP (cAMP)
fermentation
Fundamental and applied biological sciences. Psychology
Fungi - metabolism
Gene Expression Regulation, Bacterial
Gene Expression Regulation, Fungal
human health
Humans
industry
Microbiology
molecular weight
phosphoenolpyruvate: phosphotransferase system (PTS)
secondary metabolites
strain improvement
Streptomyces
Title Production of microbial secondary metabolites: Regulation by the carbon source
URI https://www.tandfonline.com/doi/abs/10.3109/10408410903489576
https://www.ncbi.nlm.nih.gov/pubmed/20210692
https://www.proquest.com/docview/2636164559
https://www.proquest.com/docview/733300666
Volume 36
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