Biosynthesis of fatty acids and triacylglycerols by 2,6,10,14-tetramethyl pentadecane-grown cells of Nocardia globerula 432

Autores
Alvarez, H.M.; Souto, M.F.; Viale, A.; Pucci, O.H.
Año de publicación
2001
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Nocardia globerula strain 432 was able to synthesize triacylglycerols (TAG) during cultivation on 2,6,10,14-tetramethyl pentadecane (pristane) under nitrogen-limiting conditions. Within these cells, 4,8,12-trimethyl tridecanoic acid was the major fatty acid detected. Fatty acids with an odd number of carbon atoms and minor amounts of even-numbered fatty acids were also observed. Experiments carried out with acrylic acid, an inhibitor of β-oxidation, suggested that odd-numbered fatty acids such as C15:0, C17:0 and 10-methyl C17:0 were synthesized de novo using propionyl-CoA, the β-oxidation product, as precursor. Although N. globerula 432 incorporated mainly straight chain fatty acids into TAG, the branched fatty acid 4,8,12-trimethyl tridecanoic acid also appeared, to some extent, in the acylglycerols. The importance of TAG biosynthesis by pristane-grown cells of N. globerula strain 432 is discussed. © 2001 Federation of European Microbiological Societies.
Fuente
FEMS Microbiol. Lett. 2001;200(2):195-200
Materia
Fatty acid
Nocardia globerula
Pristane
Triacylglycerol
2,6,10,14 tetramethyl pentadecane
4,8,12 trimethyl tridecanoic acid
acrylic acid
alkane derivative
decanoic acid derivative
fatty acid derivative
propionyl coenzyme A
triacylglycerol
unclassified drug
Actinomyces
article
cell culture
controlled study
fatty acid oxidation
fatty acid synthesis
nocardia globerula
nonhuman
priority journal
Acetates
Acrylates
Carcinogens
Drug Interactions
Fatty Acids
Nocardia
Terpenes
Triglycerides
Nivel de accesibilidad
acceso abierto
Condiciones de uso
http://creativecommons.org/licenses/by/2.5/ar
Repositorio
Biblioteca Digital (UBA-FCEN)
Institución
Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
OAI Identificador
paperaa:paper_03781097_v200_n2_p195_Alvarez

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oai_identifier_str paperaa:paper_03781097_v200_n2_p195_Alvarez
network_acronym_str BDUBAFCEN
repository_id_str 1896
network_name_str Biblioteca Digital (UBA-FCEN)
spelling Biosynthesis of fatty acids and triacylglycerols by 2,6,10,14-tetramethyl pentadecane-grown cells of Nocardia globerula 432Alvarez, H.M.Souto, M.F.Viale, A.Pucci, O.H.Fatty acidNocardia globerulaPristaneTriacylglycerol2,6,10,14 tetramethyl pentadecane4,8,12 trimethyl tridecanoic acidacrylic acidalkane derivativedecanoic acid derivativefatty acid derivativepropionyl coenzyme Atriacylglycerolunclassified drugActinomycesarticlecell culturecontrolled studyfatty acid oxidationfatty acid synthesisnocardia globerulanonhumanpriority journalAcetatesAcrylatesCarcinogensDrug InteractionsFatty AcidsNocardiaTerpenesTriglyceridesNocardia globerula strain 432 was able to synthesize triacylglycerols (TAG) during cultivation on 2,6,10,14-tetramethyl pentadecane (pristane) under nitrogen-limiting conditions. Within these cells, 4,8,12-trimethyl tridecanoic acid was the major fatty acid detected. Fatty acids with an odd number of carbon atoms and minor amounts of even-numbered fatty acids were also observed. Experiments carried out with acrylic acid, an inhibitor of β-oxidation, suggested that odd-numbered fatty acids such as C15:0, C17:0 and 10-methyl C17:0 were synthesized de novo using propionyl-CoA, the β-oxidation product, as precursor. Although N. globerula 432 incorporated mainly straight chain fatty acids into TAG, the branched fatty acid 4,8,12-trimethyl tridecanoic acid also appeared, to some extent, in the acylglycerols. The importance of TAG biosynthesis by pristane-grown cells of N. globerula strain 432 is discussed. © 2001 Federation of European Microbiological Societies.2001info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfhttp://hdl.handle.net/20.500.12110/paper_03781097_v200_n2_p195_AlvarezFEMS Microbiol. Lett. 2001;200(2):195-200reponame:Biblioteca Digital (UBA-FCEN)instname:Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturalesinstacron:UBA-FCENenginfo:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by/2.5/ar2026-04-16T09:46:43Zpaperaa:paper_03781097_v200_n2_p195_AlvarezInstitucionalhttps://digital.bl.fcen.uba.ar/Universidad públicaNo correspondehttps://digital.bl.fcen.uba.ar/cgi-bin/oaiserver.cgiana@bl.fcen.uba.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:18962026-04-16 09:46:46.26Biblioteca Digital (UBA-FCEN) - Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturalesfalse
dc.title.none.fl_str_mv Biosynthesis of fatty acids and triacylglycerols by 2,6,10,14-tetramethyl pentadecane-grown cells of Nocardia globerula 432
title Biosynthesis of fatty acids and triacylglycerols by 2,6,10,14-tetramethyl pentadecane-grown cells of Nocardia globerula 432
spellingShingle Biosynthesis of fatty acids and triacylglycerols by 2,6,10,14-tetramethyl pentadecane-grown cells of Nocardia globerula 432
Alvarez, H.M.
Fatty acid
Nocardia globerula
Pristane
Triacylglycerol
2,6,10,14 tetramethyl pentadecane
4,8,12 trimethyl tridecanoic acid
acrylic acid
alkane derivative
decanoic acid derivative
fatty acid derivative
propionyl coenzyme A
triacylglycerol
unclassified drug
Actinomyces
article
cell culture
controlled study
fatty acid oxidation
fatty acid synthesis
nocardia globerula
nonhuman
priority journal
Acetates
Acrylates
Carcinogens
Drug Interactions
Fatty Acids
Nocardia
Terpenes
Triglycerides
title_short Biosynthesis of fatty acids and triacylglycerols by 2,6,10,14-tetramethyl pentadecane-grown cells of Nocardia globerula 432
title_full Biosynthesis of fatty acids and triacylglycerols by 2,6,10,14-tetramethyl pentadecane-grown cells of Nocardia globerula 432
title_fullStr Biosynthesis of fatty acids and triacylglycerols by 2,6,10,14-tetramethyl pentadecane-grown cells of Nocardia globerula 432
title_full_unstemmed Biosynthesis of fatty acids and triacylglycerols by 2,6,10,14-tetramethyl pentadecane-grown cells of Nocardia globerula 432
title_sort Biosynthesis of fatty acids and triacylglycerols by 2,6,10,14-tetramethyl pentadecane-grown cells of Nocardia globerula 432
dc.creator.none.fl_str_mv Alvarez, H.M.
Souto, M.F.
Viale, A.
Pucci, O.H.
author Alvarez, H.M.
author_facet Alvarez, H.M.
Souto, M.F.
Viale, A.
Pucci, O.H.
author_role author
author2 Souto, M.F.
Viale, A.
Pucci, O.H.
author2_role author
author
author
dc.subject.none.fl_str_mv Fatty acid
Nocardia globerula
Pristane
Triacylglycerol
2,6,10,14 tetramethyl pentadecane
4,8,12 trimethyl tridecanoic acid
acrylic acid
alkane derivative
decanoic acid derivative
fatty acid derivative
propionyl coenzyme A
triacylglycerol
unclassified drug
Actinomyces
article
cell culture
controlled study
fatty acid oxidation
fatty acid synthesis
nocardia globerula
nonhuman
priority journal
Acetates
Acrylates
Carcinogens
Drug Interactions
Fatty Acids
Nocardia
Terpenes
Triglycerides
topic Fatty acid
Nocardia globerula
Pristane
Triacylglycerol
2,6,10,14 tetramethyl pentadecane
4,8,12 trimethyl tridecanoic acid
acrylic acid
alkane derivative
decanoic acid derivative
fatty acid derivative
propionyl coenzyme A
triacylglycerol
unclassified drug
Actinomyces
article
cell culture
controlled study
fatty acid oxidation
fatty acid synthesis
nocardia globerula
nonhuman
priority journal
Acetates
Acrylates
Carcinogens
Drug Interactions
Fatty Acids
Nocardia
Terpenes
Triglycerides
dc.description.none.fl_txt_mv Nocardia globerula strain 432 was able to synthesize triacylglycerols (TAG) during cultivation on 2,6,10,14-tetramethyl pentadecane (pristane) under nitrogen-limiting conditions. Within these cells, 4,8,12-trimethyl tridecanoic acid was the major fatty acid detected. Fatty acids with an odd number of carbon atoms and minor amounts of even-numbered fatty acids were also observed. Experiments carried out with acrylic acid, an inhibitor of β-oxidation, suggested that odd-numbered fatty acids such as C15:0, C17:0 and 10-methyl C17:0 were synthesized de novo using propionyl-CoA, the β-oxidation product, as precursor. Although N. globerula 432 incorporated mainly straight chain fatty acids into TAG, the branched fatty acid 4,8,12-trimethyl tridecanoic acid also appeared, to some extent, in the acylglycerols. The importance of TAG biosynthesis by pristane-grown cells of N. globerula strain 432 is discussed. © 2001 Federation of European Microbiological Societies.
description Nocardia globerula strain 432 was able to synthesize triacylglycerols (TAG) during cultivation on 2,6,10,14-tetramethyl pentadecane (pristane) under nitrogen-limiting conditions. Within these cells, 4,8,12-trimethyl tridecanoic acid was the major fatty acid detected. Fatty acids with an odd number of carbon atoms and minor amounts of even-numbered fatty acids were also observed. Experiments carried out with acrylic acid, an inhibitor of β-oxidation, suggested that odd-numbered fatty acids such as C15:0, C17:0 and 10-methyl C17:0 were synthesized de novo using propionyl-CoA, the β-oxidation product, as precursor. Although N. globerula 432 incorporated mainly straight chain fatty acids into TAG, the branched fatty acid 4,8,12-trimethyl tridecanoic acid also appeared, to some extent, in the acylglycerols. The importance of TAG biosynthesis by pristane-grown cells of N. globerula strain 432 is discussed. © 2001 Federation of European Microbiological Societies.
publishDate 2001
dc.date.none.fl_str_mv 2001
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/20.500.12110/paper_03781097_v200_n2_p195_Alvarez
url http://hdl.handle.net/20.500.12110/paper_03781097_v200_n2_p195_Alvarez
dc.language.none.fl_str_mv eng
language eng
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
http://creativecommons.org/licenses/by/2.5/ar
eu_rights_str_mv openAccess
rights_invalid_str_mv http://creativecommons.org/licenses/by/2.5/ar
dc.format.none.fl_str_mv application/pdf
dc.source.none.fl_str_mv FEMS Microbiol. Lett. 2001;200(2):195-200
reponame:Biblioteca Digital (UBA-FCEN)
instname:Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
instacron:UBA-FCEN
reponame_str Biblioteca Digital (UBA-FCEN)
collection Biblioteca Digital (UBA-FCEN)
instname_str Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
instacron_str UBA-FCEN
institution UBA-FCEN
repository.name.fl_str_mv Biblioteca Digital (UBA-FCEN) - Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
repository.mail.fl_str_mv ana@bl.fcen.uba.ar
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