MICROBIAL TRANSFORMATION OF ARYLPROPANOID CINNAMALDEHYDE BY THE PHYTOPATHOGEN FUNGUS <I>Colletotrichum acutatum</I>

Phytopathogenic fungi have the capacity to modify chemically a wide array of organic compounds turning them into structurally related products. In this study, biotransformation of the substrate arylpropanoid trans-cinnamaldehyde A achieved by the phylamentous phytopatogenic fungus Colletotrichum acu...

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Autores principales:	Yaned M. CORREA N., Diego L. DURANGO R., Carlos M. GARCÍA P.
Formato:	article
Lenguaje:	EN
Publicado:	Universidad de Antioquia 2009
Materias:	Antifungal activity enzymatic hydroxylation bioreduction chemoslectivity regioselectivity Food processing and manufacture TP368-456 Pharmaceutical industry HD9665-9675
Acceso en línea:	https://doaj.org/article/4eb04079602c42e9bf268e8d06726622
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spelling	oai:doaj.org-article:4eb04079602c42e9bf268e8d067266222021-11-19T04:16:25ZMICROBIAL TRANSFORMATION OF ARYLPROPANOID CINNAMALDEHYDE BY THE PHYTOPATHOGEN FUNGUS <I>Colletotrichum acutatum</I>0121-40042145-2660https://doaj.org/article/4eb04079602c42e9bf268e8d067266222009-05-01T00:00:00Zhttps://revistas.udea.edu.co/index.php/vitae/article/view/1429https://doaj.org/toc/0121-4004https://doaj.org/toc/2145-2660Phytopathogenic fungi have the capacity to modify chemically a wide array of organic compounds turning them into structurally related products. In this study, biotransformation of the substrate arylpropanoid trans-cinnamaldehyde A achieved by the phylamentous phytopatogenic fungus Colletotrichum acutatum, is evaluated; the process is carried out in liquid media culture Czapeck-Dox. The biotransformation of the substrate A produces the metabolites cinnamyl alcohol B, 3-phenyl-1-propanol C, 3-phenyloxiranemethanol D and 1-phenyl-1,3-propanediol E. The structures of metabolic products are determined by gas chromatography coupled with mass spectrometry (GC-MS) and nuclear magnetic resonance of proton and carbon (1H and 13C NMR). The process is marked by the tendency of the pathogen to produce hydroxylations on the substituent of the aromatic ring. Additionally, it has the capability to reduce the carbonyl group and the double bond. In the process, several metabolic products used like raw materials for different industries are generated. A possible metabolic pathway of the biotransformation of transcinnamaldehyde by C. acutatum is also discussed. Yaned M. CORREA N.Diego L. DURANGO R.Carlos M. GARCÍA P.Universidad de AntioquiaarticleAntifungal activityenzymatic hydroxylationbioreductionchemoslectivityregioselectivityFood processing and manufactureTP368-456Pharmaceutical industryHD9665-9675ENVitae, Vol 16, Iss 1 (2009)
institution	DOAJ
collection	DOAJ
language	EN
topic	Antifungal activity enzymatic hydroxylation bioreduction chemoslectivity regioselectivity Food processing and manufacture TP368-456 Pharmaceutical industry HD9665-9675
spellingShingle	Antifungal activity enzymatic hydroxylation bioreduction chemoslectivity regioselectivity Food processing and manufacture TP368-456 Pharmaceutical industry HD9665-9675 Yaned M. CORREA N. Diego L. DURANGO R. Carlos M. GARCÍA P. MICROBIAL TRANSFORMATION OF ARYLPROPANOID CINNAMALDEHYDE BY THE PHYTOPATHOGEN FUNGUS <I>Colletotrichum acutatum</I>
description	Phytopathogenic fungi have the capacity to modify chemically a wide array of organic compounds turning them into structurally related products. In this study, biotransformation of the substrate arylpropanoid trans-cinnamaldehyde A achieved by the phylamentous phytopatogenic fungus Colletotrichum acutatum, is evaluated; the process is carried out in liquid media culture Czapeck-Dox. The biotransformation of the substrate A produces the metabolites cinnamyl alcohol B, 3-phenyl-1-propanol C, 3-phenyloxiranemethanol D and 1-phenyl-1,3-propanediol E. The structures of metabolic products are determined by gas chromatography coupled with mass spectrometry (GC-MS) and nuclear magnetic resonance of proton and carbon (1H and 13C NMR). The process is marked by the tendency of the pathogen to produce hydroxylations on the substituent of the aromatic ring. Additionally, it has the capability to reduce the carbonyl group and the double bond. In the process, several metabolic products used like raw materials for different industries are generated. A possible metabolic pathway of the biotransformation of transcinnamaldehyde by C. acutatum is also discussed.
format	article
author	Yaned M. CORREA N. Diego L. DURANGO R. Carlos M. GARCÍA P.
author_facet	Yaned M. CORREA N. Diego L. DURANGO R. Carlos M. GARCÍA P.
author_sort	Yaned M. CORREA N.
title	MICROBIAL TRANSFORMATION OF ARYLPROPANOID CINNAMALDEHYDE BY THE PHYTOPATHOGEN FUNGUS <I>Colletotrichum acutatum</I>
title_short	MICROBIAL TRANSFORMATION OF ARYLPROPANOID CINNAMALDEHYDE BY THE PHYTOPATHOGEN FUNGUS <I>Colletotrichum acutatum</I>
title_full	MICROBIAL TRANSFORMATION OF ARYLPROPANOID CINNAMALDEHYDE BY THE PHYTOPATHOGEN FUNGUS <I>Colletotrichum acutatum</I>
title_fullStr	MICROBIAL TRANSFORMATION OF ARYLPROPANOID CINNAMALDEHYDE BY THE PHYTOPATHOGEN FUNGUS <I>Colletotrichum acutatum</I>
title_full_unstemmed	MICROBIAL TRANSFORMATION OF ARYLPROPANOID CINNAMALDEHYDE BY THE PHYTOPATHOGEN FUNGUS <I>Colletotrichum acutatum</I>
title_sort	microbial transformation of arylpropanoid cinnamaldehyde by the phytopathogen fungus <i>colletotrichum acutatum</i>
publisher	Universidad de Antioquia
publishDate	2009
url	https://doaj.org/article/4eb04079602c42e9bf268e8d06726622
work_keys_str_mv	AT yanedmcorrean microbialtransformationofarylpropanoidcinnamaldehydebythephytopathogenfungusicolletotrichumacutatumi AT diegoldurangor microbialtransformationofarylpropanoidcinnamaldehydebythephytopathogenfungusicolletotrichumacutatumi AT carlosmgarciap microbialtransformationofarylpropanoidcinnamaldehydebythephytopathogenfungusicolletotrichumacutatumi
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MICROBIAL TRANSFORMATION OF ARYLPROPANOID CINNAMALDEHYDE BY THE PHYTOPATHOGEN FUNGUS <I>Colletotrichum acutatum</I>

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