Enzymatic synthesis of perlauric acid using Novozym 435

For the biocatalytic synthesis of perlauric acid, Novozym 435 (Candida antarctica lipase immobilized on polyacrylic resin) was found to be the most active catalyst and toluene was the most suitable solvent. The effects of various parameters on conversion and rates of reaction were studied in the abs...

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Main Authors: Yadav, Ganapati D., Manjula Devi, K.
Format: Article in Journal/Newspaper
Language:unknown
Published: Elsevier Science 2002
Subjects:
Online Access:http://repository.ias.ac.in/111860/
http://www.sciencedirect.com/science/article/pii/S1369703X01001644
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spelling ftindianacasci:oai:repository.ias.ac.in:111860 2023-05-15T13:39:33+02:00 Enzymatic synthesis of perlauric acid using Novozym 435 Yadav, Ganapati D. Manjula Devi, K. 2002-03 http://repository.ias.ac.in/111860/ http://www.sciencedirect.com/science/article/pii/S1369703X01001644 unknown Elsevier Science Yadav, Ganapati D. Manjula Devi, K. (2002) Enzymatic synthesis of perlauric acid using Novozym 435 Biochemical Engineering Journal, 10 (2). pp. 93-101. ISSN 1369-703X T Technology (General) Article PeerReviewed 2002 ftindianacasci 2017-09-22T22:09:35Z For the biocatalytic synthesis of perlauric acid, Novozym 435 (Candida antarctica lipase immobilized on polyacrylic resin) was found to be the most active catalyst and toluene was the most suitable solvent. The effects of various parameters on conversion and rates of reaction were studied in the absence of mass transfer limitations. Reusability studies indicated that there was enzyme deactivation and from a preliminary study of the deactivation, it was observed that the deactivation obeys a pseudo-first-order model. Lineweaver–Burk plots indicated the formation of a ternary complex. A model based on ordered bi–bi mechanism was found to fit the initial rate data very well and using this model, some kinetic parameters were calculated by non-linear regression analysis. Article in Journal/Newspaper Antarc* Antarctica Indian Academy of Sciences: Publication of Fellows
institution Open Polar
collection Indian Academy of Sciences: Publication of Fellows
op_collection_id ftindianacasci
language unknown
topic T Technology (General)
spellingShingle T Technology (General)
Yadav, Ganapati D.
Manjula Devi, K.
Enzymatic synthesis of perlauric acid using Novozym 435
topic_facet T Technology (General)
description For the biocatalytic synthesis of perlauric acid, Novozym 435 (Candida antarctica lipase immobilized on polyacrylic resin) was found to be the most active catalyst and toluene was the most suitable solvent. The effects of various parameters on conversion and rates of reaction were studied in the absence of mass transfer limitations. Reusability studies indicated that there was enzyme deactivation and from a preliminary study of the deactivation, it was observed that the deactivation obeys a pseudo-first-order model. Lineweaver–Burk plots indicated the formation of a ternary complex. A model based on ordered bi–bi mechanism was found to fit the initial rate data very well and using this model, some kinetic parameters were calculated by non-linear regression analysis.
format Article in Journal/Newspaper
author Yadav, Ganapati D.
Manjula Devi, K.
author_facet Yadav, Ganapati D.
Manjula Devi, K.
author_sort Yadav, Ganapati D.
title Enzymatic synthesis of perlauric acid using Novozym 435
title_short Enzymatic synthesis of perlauric acid using Novozym 435
title_full Enzymatic synthesis of perlauric acid using Novozym 435
title_fullStr Enzymatic synthesis of perlauric acid using Novozym 435
title_full_unstemmed Enzymatic synthesis of perlauric acid using Novozym 435
title_sort enzymatic synthesis of perlauric acid using novozym 435
publisher Elsevier Science
publishDate 2002
url http://repository.ias.ac.in/111860/
http://www.sciencedirect.com/science/article/pii/S1369703X01001644
genre Antarc*
Antarctica
genre_facet Antarc*
Antarctica
op_relation Yadav, Ganapati D.
Manjula Devi, K. (2002) Enzymatic synthesis of perlauric acid using Novozym 435 Biochemical Engineering Journal, 10 (2). pp. 93-101. ISSN 1369-703X
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