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Diacylglycerol production by genetically modified lipase from Malassezia globosa

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논문

Diacylglycerol production by genetically modified lipase from Malassezia globosa

학술지

Journal of molecular catalysis. B, Enzymatic

저자명

Li, Daoming; Khan, Faez Iqbal; Zhao, Zexin; Wang, Weifei; Yang, Bo; Wang, Yonghua

초록

<P><B>Abstract</B></P> <P>Diacylglycerol (DAG)-enriched oil has drawn considerable attention for the prevention of obesity and other lifestyle-related diseases. In this study, a mutant lipase of SMG1 (SMG1-F278D) from <I>Malassezia globosa</I> was studied for the production of DAG. The SMG1-F278D exhibited 4-fold increased esterification activity as well as superior fatty acid (FA) specificity for medium chain FAs. Molecular docking study suggested that the caprylic acid (CA) was strongly bound to the catalytic residue Ser171 present in the SMG1-F278D as compared to SMG1. Molecular Dynamics (MD) simulations were employed in order to understand the structural conformations of SMG1 and SMG1-F278D. The structure of SMG1-F278D was found to be more compact as well as less deviated from its native conformation. There was an increase in &beta;-sheet as well as &alpha;-helix in the SMG1-F278D that may stabilize the protein structure due to point mutation. Finally, the capability of SMG1-F278D in synthesis of DAG was evaluated. Effects of reaction parameters such as substrate molar ratio of glycerol to FAs, enzyme loading and reaction temperature on the esterification were investigated. The optimal reaction conditions were achieved as 4:1 molar ratio of glycerol to FAs, enzyme loading of 100U/g (U/w, with respect to the total substrates) and temperature of 25&deg;C. The present study provides important information about SMG1 mutant for better utilization in the oils and fats industries.</P> <P><B>Highlights</B></P> <P> <UL> <LI> SMG1-F278D was studied for the production of DAG. </LI> <LI> SMG1-F278D exhibited 4-fold increased esterification activity as well as superior FA specificity towards medium chain FAs. </LI> <LI> Molecular docking suggested that caprylic acid strongly bound to the catalytic pocket of SMG1-F278D. </LI> <LI> MD simulations suggested the stable nature of SMG1-F278D due to increase in &beta;-sheet and &alpha;-helix. </LI> <LI> Further, the esterification process for the production of DAG was optimized. </LI> </UL> </P> <P><B>Graphical abstract</B></P> <P>[DISPLAY OMISSION]</P>

발행연도

2016

발행기관

Elsevier

ISSN

1381-1177

ISSN

1873-3158

133

suppl1

페이지

pp.S204-S212

주제어

Diacylglycerol; Mono- and diacylglycerol lipase; Esterification; Molecular docking; Molecular dynamics simulations

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1 2023-12-11

논문; 2016-11-01

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