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Use of the Plant as Biocatalysts for Producing Enantiomerically Pure Seconder Alcohol

dc.authorscopusid 56584750400
dc.authorscopusid 7003665652
dc.authorwosid Mehmetoğlu, Ülkü/Aah-7637-2019
dc.contributor.author Kazici, Hilal Celik
dc.contributor.author Mehmetoglu, Ulku
dc.date.accessioned 2025-05-10T17:58:01Z
dc.date.available 2025-05-10T17:58:01Z
dc.date.issued 2015
dc.department T.C. Van Yüzüncü Yıl Üniversitesi en_US
dc.department-temp [Kazici, Hilal Celik] Yuzuncu Yil Univ, Muhendisl Mimarl Fak, Kimya Muh Bol, Van, Turkey; [Mehmetoglu, Ulku] Ankara Univ, Muhendisl Fak, Kimya Muh Bol, TR-06100 Ankara, Turkey en_US
dc.description.abstract In this study, enantiomerically pure (S)-1-Phenylethanol was produced with bioreduction of acetophenone that the precursor of many pharmacological product. Derivatives of (S)-1-Phenylethanol (secondary alcohol) is used as the active ingredient of drug of anti alzheimer. Production of (S)-1-Phenylethanol was conducted with the asymmetric reduction reaction of acetophenone that biocatalyst for there action is enzyme of alcohol dehydrogenase (ADH). In this study, a variety of fruits and vegetables were used as source of enzyme (ADH) for reduction of the carbonyl group and ADH enzyme activities were determined of different plants (carrots, potatoes, grapes, radishes) for selection of suitable plant which it has the highest intra cellular enzyme activity. At the end of this election carrot has been considered as a biocatalyst which has highest ADH activity. The effects of size of biyocatalyst, source of enzyme, substrate concentration, temperature, reaction time, pH of there action and the amount of biocatalyst have been investigated on the production of (S)-1-Phenylethanol. It was found that ADH enzyme in fresh carrots catalysed the bioselective asymmetric reduction reactions at high conversion and high enantioselectively (>% 99 ee and 92% c), under the conditions of 2mM substrate concentration, 200 g/L biocatalyst concentration, 1,52 mm biyocatalyst size, reaction temperature 33 degrees C, pH=7 and 150 rpm agitation speed. en_US
dc.description.woscitationindex Science Citation Index Expanded
dc.identifier.endpage 56 en_US
dc.identifier.issn 1300-1884
dc.identifier.issn 1304-4915
dc.identifier.issue 1 en_US
dc.identifier.scopus 2-s2.0-84926462609
dc.identifier.scopusquality Q3
dc.identifier.startpage 49 en_US
dc.identifier.uri https://hdl.handle.net/20.500.14720/20227
dc.identifier.volume 30 en_US
dc.identifier.wos WOS:000352627600006
dc.identifier.wosquality Q4
dc.language.iso tr en_US
dc.publisher Gazi Univ, Fac Engineering Architecture en_US
dc.relation.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
dc.rights info:eu-repo/semantics/closedAccess en_US
dc.subject Bioreduction en_US
dc.subject Asymmetric Synthesis en_US
dc.subject Acetophenone en_US
dc.subject (S)-1-Phenylethanol en_US
dc.subject Alcoholdehydrogenase en_US
dc.subject Plant en_US
dc.title Use of the Plant as Biocatalysts for Producing Enantiomerically Pure Seconder Alcohol en_US
dc.type Article en_US

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