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
.jpg)
- Institución
- Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
- OAI Identificador
- paperaa:paper_03781097_v200_n2_p195_Alvarez
Ver los metadatos del registro completo
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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 |
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http://hdl.handle.net/20.500.12110/paper_03781097_v200_n2_p195_Alvarez |
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http://hdl.handle.net/20.500.12110/paper_03781097_v200_n2_p195_Alvarez |
| dc.language.none.fl_str_mv |
eng |
| language |
eng |
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info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar |
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openAccess |
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http://creativecommons.org/licenses/by/2.5/ar |
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application/pdf |
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