02462nas a2200277   4500008004100000022001400041245015600055210006900211260000900280300001200289490000800301520151800309653001401827653000901841653003201850653001401882653002201896653002401918100001701942700002001959700002001979700001601999700002102015700002202036856012602058       2018                        eng d  a0360-544200aOptimization of the in situ transesterification step for biodiesel production using biomass of Yarrowia lipolytica NCIM 3589 grown on waste cooking oil0 aOptimization of the in situ transesterification step for biodies  cJAN   a944-9520 v1423 a<p>The in situ (one-step) acid-catalyzed transesterification step for conversion to biodiesel of biomass from oleaginous yeast Yarrowia lipolytica grown on waste cooking oil (WCO) is studied. The process yield of biodiesel was optimized by investigating effects of various parameters, namely, biomass, methanol, chloroform, catalyst, temperature, time and sonication. A Plackett-Burman statistical design of experiments revealed that biomass is the most significant factor influencing biodiesel (FAME, fatty acid methyl ester) production. Subsequently, a one variable design (OVD) of experiments for increased biomass loadings showed higher yields of FAME with no additional requirement of reactants, solvents or special equipment. The biomass grown on WCO had a lipid productivity of 0.042 g L-1 h(-1) and 4 g of this loading gave a high FAME yield of 0.88 gin 8 hat 50 degrees C with methanol: chloroform (10:1) and acid catalyst (0.2 M H2SO4,1.0 ml g(-1)). The FAME profile had desirable amounts of saturated (32.81%), monounsaturated (36.41%), polyunsaturated (30.59%) methyl esters. The predicted and experimentally determined physico-chemical properties of FAME were found in accordance with specified international standards. Thus, the direct one-pot in situ transesterification reaction using Y. lipolytica biomass grown on WCO provides a high yield of biodiesel with potential applicability while simultaneously addressing the management of this pollutant. (C) 2017 Elsevier Ltd. All rights reserved.</p>10aBiodiesel10aFAME10aIn situ transesterification10aOne -step10aWaste cooking oil10aYarrowia lipolytica1 aKatre, Gouri1 aRaskar, Shubham1 aZinjarde, Smita1 aKumar, Ravi1 aKulkarni, B., D.1 aRaviKumar, Ameeta  uhttps://library.ncl.res.in/content/optimization-situ-transesterification-step-biodiesel-production-using-biomass-yarrowia02156nas a2200229   4500008004100000022001400041245010800055210006900163260000900232300000700241490000700248520134100255653002701596653001701623653003401640653003301674653002401707100002601731700001601757700002401773856012901797       2023                        eng d  a2191-085500aPotential of Y. lipolytica epoxide hydrolase for efficient production of enantiopure (R)-1,2-octanediol0 aPotential of Y lipolytica epoxide hydrolase for efficient produc  cJUL   a770 v133 a<p>
	The recombinant Yleh from a tropical marine yeast Yarrowia lipolytica NCIM 3589 exhibited a high epoxide hydrolase activity of 9.34 +/- 1.80 mu mol min(-1) mg(-1) protein towards 1,2-epoxyoctane (EO), at pH 8.0 and 30 degrees C. The reaction product was identified as 1,2-Octanediol (OD) by GC-MS using EO and H2O18 as substrate, affirming the functionality of Yleh as an epoxide hydrolase. For EO, the K-m, V-max, and k(cat)/K-m values were 0.43 +/- 0.017 mM, 0.042 +/- 0.003 mM min(-1), and 467.17 +/- 39.43 mM(-1) min(-1), respectively. To optimize the reaction conditions for conversion of racemic EO by Yleh catalyst to enantiopure (R)-1,2-octanediol, initially, Response Surface Methodology was employed. Under optimized reaction conditions of 15 mM EO, 150 mu g purified Yleh at 30 degrees C a maximal diol production of 7.11 mM was attained in a short span of 65 min with a yield of 47.4%. Green technology using deep eutectic solvents for the hydrophobic substrate (EO) were tested as co-solvents in Yleh catalyzed EO hydrolysis. Choline chloride-Glycerol, produced 9.08 mM OD with an increased OD yield of 60.5%. Thus, results showed that deep eutectic solvents could be a promising solvent for Yleh-catalyzed reactions making Yleh a potential biocatalyst for the biosynthesis of enantiopure synthons. [GRAPHICS] .</p>
10aDeep Eutectic solvents10aOptimization10aRecombinant epoxide hydrolase10aResponse surface methodology10aYarrowia lipolytica1 aGodase, Vijaya, P. P.1 aKumar, Ravi1 aKumar, Ameeta, Ravi  uhttps://library.ncl.res.in/content/potential-y-lipolytica-epoxide-hydrolase-efficient-production-enantiopure-r-12-octanediol