首页> 外文期刊>Journal of molecular catalysis, B. Enzymatic >Biosynthesis of ethyl esters of short-chain fatty acids using whole-cell lipase from Rhizopus chinesis CCTCC M201021 in non-aqueous phase
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Biosynthesis of ethyl esters of short-chain fatty acids using whole-cell lipase from Rhizopus chinesis CCTCC M201021 in non-aqueous phase

机译:非水相中根霉根茎全细胞脂肪酶CCTCC M201021的全细胞脂肪酶生物合成短链脂肪酸乙酯

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A fungal strain capable of synthesizing ethyl esters of short-chain fatty acids was isolated from leaven (mouldy grains) samples through combined screening strategy of lipolysis and with esterification ability and was identified to be Rhizopus chinesis CCTCC M201021. When compared with other 10 commercial lipases, the whole-cell lipase of R. chinesis CCTCC M201021 (RCL) showed much higher ability in the synthesis of ethyl hexanoate during the screening of suitable lipases with a maximum yield of 96.5% after 72 h conversion using 0.5 M equal molar substrate concentration. Thereafter, the effect of important reaction parameters for enhancing ester formation by whole-cell RCL was investigated in this study. Higher esterification (>90%) was observed and maintained under chain length of carboxylic acids (C-2-C-8), Solvents with log P (P: partition coefficient) >2.0 enhanced RCL activity to give high conversion (>88.8%). Effect of temperature on reaction showed better esterification at 30-40degreesC. Increase in concentration of substrates (ethanol and acid) from 0,2 to 1.4 M led to decrease in molar conversion from 96 to 85% in the synthesis of ethyl hexanoate. Changing the molar ratio of acid/ethanol from 1:1 to 1:3 at 0.6M acid concentration resulted in a maximal conversion of 98.5% at the ratio of 1:1.3, It was observed that better esterification could be achieved with initial water activity (a(w)) ranging from 0.66 to 0.97. A crucial enzyme concentration of 6 g/l was chosen for research after effect on esterification reaction was examined. The half-life period of esterification for different flavor ester production indicated that whole-cell RCL was more stable in batch esterification reaction within 840-975 h of half-life period for ethyl flavor esters. (C) 2002 Elsevier Science B.V. All rights reserved. [References: 19]
机译:通过脂肪分解和酯化作用的联合筛选策略,从酵母(发霉的谷物)样品中分离出能够合成短链脂肪酸乙酯的真菌菌株,并将其鉴定为中国根霉CCTCC M201021。当与其他10种商业脂肪酶比较时,在筛选合适的脂肪酶的过程中,中国R. chinesis CCTCC M201021(RCL)的全细胞脂肪酶显示出更高的合成己酸乙酯的能力,使用72 h转化后最大产率为96.5%。 0.5 M等摩尔底物浓度。此后,本研究研究了重要反应参数对全细胞RCL增强酯形成的影响。观察到较高的酯化(> 90%),并在羧酸(C-2-C-8)的链长下保持不变。log P(P:分配系数)> 2.0的溶剂增强了RCL活性,从而获得高转化率(> 88.8%) )。温度对反应的影响在30-40℃下显示出更好的酯化。在己酸乙酯的合成中,底物(乙醇和酸)的浓度从0.2增加到1.4 M,导致摩尔转化率从96降低到85%。在0.6M的酸浓度下,将酸/乙醇的摩尔比从1:1更改为1:3导致在1:1.3的比例下最大转化率为98.5%,观察到初始水活度可以实现更好的酯化(a(w))介于0.66至0.97之间。在研究了对酯化反应的影响后,选择了6 g / l的关键酶浓度进行研究。不同风味酯生产的酯化反应的半衰期表明,在乙基风味酯半衰期的840-975小时内,全细胞RCL在间歇酯化反应中更稳定。 (C)2002 Elsevier Science B.V.保留所有权利。 [参考:19]

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