BIOTRANSFORMATION OF THE COMPOUNDS 2-PHENYLETHANOL AND ACETOPHENONE BY THE PHYTOPHATOGEN FUNGUS <I>Botryodiplodia theobromae</I>

In this study, biotransformations of the substrates 2-phenilethanol 1 and acetophenone 2 achieve by the phylamentous phytopatogenic fungus Botryodiplodia theobromae, are evaluated; the process is carried out in liquid media culture Czapeck-Dox to an average temperature 24 ºC, relative humidity betwe...

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Autores principales: Rodrigo VELASCO B., Iván D. VALVERDE P., Diego L. DURANGO R., Carlos M. GARCÍA P.
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Publicado: Universidad de Antioquia 2009
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Acceso en línea:https://doaj.org/article/d3dcacb2045443daa302ec4a3962a91f
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spelling oai:doaj.org-article:d3dcacb2045443daa302ec4a3962a91f2021-11-19T04:21:05ZBIOTRANSFORMATION OF THE COMPOUNDS 2-PHENYLETHANOL AND ACETOPHENONE BY THE PHYTOPHATOGEN FUNGUS <I>Botryodiplodia theobromae</I>0121-40042145-2660https://doaj.org/article/d3dcacb2045443daa302ec4a3962a91f2009-02-01T00:00:00Zhttps://revistas.udea.edu.co/index.php/vitae/article/view/607https://doaj.org/toc/0121-4004https://doaj.org/toc/2145-2660In this study, biotransformations of the substrates 2-phenilethanol 1 and acetophenone 2 achieve by the phylamentous phytopatogenic fungus Botryodiplodia theobromae, are evaluated; the process is carried out in liquid media culture Czapeck-Dox to an average temperature 24 ºC, relative humidity between 45 % to 60 % and with agitation in shaker 150 rpm. The pathogen is obtained from infected commercial fruits of avocado, acquired at the centers of trade in the city of Medellín (Antioquia-Colombia) and it is characterized morphologically in the Phytopathology Laboratory of the University National Colombia, Medellín. The biotransformation of the substrate 1 produces the metabolites phenylethanodiol 3, 2- phenylacetic acid 4, phenylacetate 2-phenylethyl 5, acetate of 2-phenylethanol 6, and from substrate 2 are obtained the metabolites 1-phenylethanol 7, 2-phenilacetic acid 6, 2-phenylethanol 1, 2-phenylethanal 8, o-hydroxiacetophenone 9 and acetate of 1-phenylethanol 10. 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 tendency of the pathogen to produce hydroxylations on the alkylic chain and some on the aromatic chain. Additionally, it has the capability to reduce to the carbonyl group and produce esterification reaction in the hydroxyl groups. Rodrigo VELASCO B.Iván D. VALVERDE P.Diego L. DURANGO R.Carlos M. GARCÍA P.Universidad de AntioquiaarticleEnzymatic hydroxylationsenzymatic reduction of aromatic ketoneenzymatic esterificationFood processing and manufactureTP368-456Pharmaceutical industryHD9665-9675ENVitae, Vol 14, Iss 2 (2009)
institution DOAJ
collection DOAJ
language EN
topic Enzymatic hydroxylations
enzymatic reduction of aromatic ketone
enzymatic esterification
Food processing and manufacture
TP368-456
Pharmaceutical industry
HD9665-9675
spellingShingle Enzymatic hydroxylations
enzymatic reduction of aromatic ketone
enzymatic esterification
Food processing and manufacture
TP368-456
Pharmaceutical industry
HD9665-9675
Rodrigo VELASCO B.
Iván D. VALVERDE P.
Diego L. DURANGO R.
Carlos M. GARCÍA P.
BIOTRANSFORMATION OF THE COMPOUNDS 2-PHENYLETHANOL AND ACETOPHENONE BY THE PHYTOPHATOGEN FUNGUS <I>Botryodiplodia theobromae</I>
description In this study, biotransformations of the substrates 2-phenilethanol 1 and acetophenone 2 achieve by the phylamentous phytopatogenic fungus Botryodiplodia theobromae, are evaluated; the process is carried out in liquid media culture Czapeck-Dox to an average temperature 24 ºC, relative humidity between 45 % to 60 % and with agitation in shaker 150 rpm. The pathogen is obtained from infected commercial fruits of avocado, acquired at the centers of trade in the city of Medellín (Antioquia-Colombia) and it is characterized morphologically in the Phytopathology Laboratory of the University National Colombia, Medellín. The biotransformation of the substrate 1 produces the metabolites phenylethanodiol 3, 2- phenylacetic acid 4, phenylacetate 2-phenylethyl 5, acetate of 2-phenylethanol 6, and from substrate 2 are obtained the metabolites 1-phenylethanol 7, 2-phenilacetic acid 6, 2-phenylethanol 1, 2-phenylethanal 8, o-hydroxiacetophenone 9 and acetate of 1-phenylethanol 10. 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 tendency of the pathogen to produce hydroxylations on the alkylic chain and some on the aromatic chain. Additionally, it has the capability to reduce to the carbonyl group and produce esterification reaction in the hydroxyl groups.
format article
author Rodrigo VELASCO B.
Iván D. VALVERDE P.
Diego L. DURANGO R.
Carlos M. GARCÍA P.
author_facet Rodrigo VELASCO B.
Iván D. VALVERDE P.
Diego L. DURANGO R.
Carlos M. GARCÍA P.
author_sort Rodrigo VELASCO B.
title BIOTRANSFORMATION OF THE COMPOUNDS 2-PHENYLETHANOL AND ACETOPHENONE BY THE PHYTOPHATOGEN FUNGUS <I>Botryodiplodia theobromae</I>
title_short BIOTRANSFORMATION OF THE COMPOUNDS 2-PHENYLETHANOL AND ACETOPHENONE BY THE PHYTOPHATOGEN FUNGUS <I>Botryodiplodia theobromae</I>
title_full BIOTRANSFORMATION OF THE COMPOUNDS 2-PHENYLETHANOL AND ACETOPHENONE BY THE PHYTOPHATOGEN FUNGUS <I>Botryodiplodia theobromae</I>
title_fullStr BIOTRANSFORMATION OF THE COMPOUNDS 2-PHENYLETHANOL AND ACETOPHENONE BY THE PHYTOPHATOGEN FUNGUS <I>Botryodiplodia theobromae</I>
title_full_unstemmed BIOTRANSFORMATION OF THE COMPOUNDS 2-PHENYLETHANOL AND ACETOPHENONE BY THE PHYTOPHATOGEN FUNGUS <I>Botryodiplodia theobromae</I>
title_sort biotransformation of the compounds 2-phenylethanol and acetophenone by the phytophatogen fungus <i>botryodiplodia theobromae</i>
publisher Universidad de Antioquia
publishDate 2009
url https://doaj.org/article/d3dcacb2045443daa302ec4a3962a91f
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