Enzymatic synthesis of water-soluble derivatives of salicylic acid in organic media

A novel enzymatic method for preparing water-soluble derivatives of salicylic acid catalyzed by immobilized lipase was described. This study is the first to describe the enzymatic transesterification of methyl salicylate in organic solvents with different hydroxyl donors. The acyl-transfer between methyl salicylate and sorbitol was best supported by solvents of log P values –0.33 to 1.4. With Candida antarctica lipase in tert-amyl alcohol, a sorbitol conversion yield of 98% can be obtained by transesterification with sorbitol and methyl salicylate in one step.     

Selective enzymatic preparation of vinyl sugar esters using DMSO as a denaturing co-solvent

The protease-catalyzed transesterifications between hexoses and divinyladipate were examined. In dimethylformamide hexoses such as d-glucose, d-mannose, d-galactose and -methyl d-galactoside were esterified with divinyladipate by alkaline protease from Streptomyces sp. to give corresponding 6-O-vinyl adipoyl sugars. When the denaturing cosolvent, DMSO, was added to the solvent, galactose was selectively esterified at only the C-2 position.     

Large-scale biodiesel production from microalga Chlorella protothecoides through heterotrophic cultivation in bioreactors

An integrated approach of biodiesel production from heterotrophic Chlorella protothecoides focused on scaling up fermentation in bioreactors was reported in this study. Through substrate feeding and fermentation process controls, the cell density of C. protothecoides achieved 15.5 g L(-1) in 5 L, 12.8 g L(-1) in 750 L, and 14.2 g L(-1) in 11,000 L bioreactors, respectively. Resulted from heterotrophic metabolism, the lipid content reached 46.1%, 48.7%, and 44.3% of cell dry weight in samples from 5 L, 750 L, and 11,000 L bioreactors, respectively. Transesterification of the microalgal oil was catalyzed by immobilized lipase from Candidia sp. 99-125. With 75% lipase (12,000 U g(-1), based on lipid quantity) and 3:1 molar ratio of methanol to oil batch-fed at three times, 98.15% of the oil was converted to monoalkyl esters of fatty acids in 12 h. The expanded biodiesel production rates were 7.02 g L(-1), 6.12 g L(-1), and 6.24 g L(-1) in 5 L, 750 L, and 11,000 L bioreactors, respectively. The properties of biodiesel from Chlorella were comparable to conventional diesel fuel and comply with the US Standard for Biodiesel (ASTM 6751). These results suggest that it is feasible to expand heterotrophic Chlorella fermentation for biodiesel production at the industry level.     

Resolution of racemic carboxylic acids via the lipase‐catalyzed irreversible transesterification of vinyl esters

The lipase‐catalyzed irreversible transesterification procedure using vinyl esters was applied to the resolution of racemic 2‐phenoxypropanoic acids. Aspergillus niger lipase showed high enantioselectivities and reasonable reaction rates. The enantioselectivity was found to be affected profoundly by several variables, e.g., the alcohol as nucleophile, the organic solvent used, and the reaction temperature. A gram‐scale resolution of (RS)‐2‐phenoxypropanoic acid was achieved after optimization of the reaction conditions. Then this irreversible transesterification procedure was applied to the resolution of some related 2‐substituted carboxylic acids. Thus, racemic 2‐methoxy‐2‐phenylacetic acid was resolved via the A. niger lipase‐catalyzed transesterification of the corresponding vinyl ester. 2‐Phenylpropanoic acid and 2‐phenylbutanoic acid were resolved using Pseudomonas sp. lipase. A gram‐scale resolution of 2‐phenylbutanoic acid was achieved by this procedure coupled with the porcine liver esterase‐catalyzed hydrolysis of the resulting methyl ester. Chirality 11:554–560, 1999. © 1999 Wiley‐Liss, Inc.     

有机相中酶促有机硅烷醇的转酯

在有机介质中,脂肪酶L-1754可以催化非天然有机硅烷醇与脂肪酸酯的转酯反应.反应介质、反应体系水活度和底物的结构对酶促转酯反应有显著的影响.适宜的反应介质为正辛烷,反应体系最适水活度为0.55.     

Chromobacterium viscosum lipase catalyzes the transesterifications at the carboxyl site as well as the hydroxy site during the enzymatic enantioselective alcoholysis of O-acylated mandelates

During the enzyme-catalyzed deacylation of O-acylated mandelates with an alcohol, Chromobacterium viscosum lipase was found to catalyze the transesterifications not only at the hydroxy site but also at the carboxyl site of mandelic acids, while such a side-reaction at the carboxyl site was negligible with the other lipases examined.     

脂肪酶催化合成生物柴油的研究

生物柴油是用动植物油脂或长链脂肪酸与甲醇等低碳醇合成的脂肪酸甲酯,是一种替代能源。这里探讨了生物法制备生物柴油的过程,采用脂肪酶酯化和酯交换两条工艺路线进行催化合成。深入研究制备过程中,不同脂肪酶、酶的用量和纯度、有机溶剂、低碳醇的抑制作用、吸水剂的作用、反应时间和进程、底物的特异性和底物摩尔比等参数对酯化过程的影响。试验结果表明,采用最佳酯化反应参数和分批加入甲醇并用硅胶作脱水剂的工艺过程,酯化率可以达到92％,经分离纯化后的产品GC分析的纯度可达98％以上,固定化酶的使用半衰期可达到360h。同时对酯交换制备生物柴油过程中,甲醇的用量和甲醇的加入方式对脂肪酶催化过程的影响作了初步研究,优化后的酯交换率可达到83％。     

研究开发燃料油植物生产生物柴油的几个策略

能源短缺和环境污染是目前人类社会所面临的巨大挑战,而生物柴油的应用和推广正是现阶段解决能源替代问题的较佳手段。现今国外生物柴油产业发展十分迅速,产量逐年增长,而我国的生物柴油产业才刚刚起步。本文介绍了极具潜力的5种木本油料植物麻疯树（Jatropha curcas）、光皮树（Cornus wilsoniana）、文冠果（Xanthoceras sorbifolia）、黄连木（Pistacia chinensis）和欧李（Cerasus humilis）和1种野生草本油料植物海篷子（Salicornia bigelivii）,进而提出运用转基因技术提高燃料油植物种子含油量的优势,归纳总结了生产生物柴油的4种不同工艺。最后建议政府应对燃料油植物种植和生产加工产业实施补贴和免税等扶植政策。本文对我国生物质能源产业的发展提供了有价值的实施策略,具有重要的借鉴和参考价值。     

固定化脂肪酶催化制备L-薄荷醇

用大孔树脂NKA固定高选择性的脂肪酶,催化有机相中转酯化反应,从而拆分八异构体消旋薄荷醇来制备L-薄荷醇。研究pH、载体与酶比例对固定化酶制备的影响及固定化酶的反应稳定性;考察温度、转酯化过程醇酯比例、及底物醇异构组成变化对拆分效果的影响。结果表明:固定化酶的最适pH为8,载体与酶的比例为5∶1时,所得固定化酶的反应稳定性比游离酶的反应稳定性提高了约50%;转酯化反应的最优温度为40℃,醇酯比例为1.5∶1时最佳,改进八异构体消旋薄荷醇组分比例后,非对映体选择率dep达到了95.1%。     

几种离子液体的微波法合成及其对脂肪酶催化效果的影响

采用微波法合成9种目标离子液体,对中间体[Bmim]Br的合成条件及其离子液体对全细胞催化剂催化效果的影响进行考察.直接将产脂肪酶真菌粗状假丝酵母(Candida valida) T2细胞固定在聚氨酯颗粒中,制备固定化细胞催化剂,将其应用于合成离子液体介质中催化甲醇与大豆油酯交换反应制备生物柴油.结果表明:微波功率200 W下间隙照射100 s,中间体[Bmim]Br的收率达95.16%,有效地提高了离子液合成产率;在[Bmim]PF6离子液中固定化细胞酶催化转酯化反应30 h,大豆油的转化率达42%,反应效果较其他8种合成离子液体好;固定化细胞颗粒和[Bmim]PF6重复使用4次,其油脂转化率和酶活保持率分别达到29%和69%,表现出较好的催化反应稳定性.