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新型耐温耐碱脂肪酶的:统计优化、酶纯化、固定化及其在生物柴油生产中的应用。

Thermo-alkali-stable lipase from a novel : statistical optimization, enzyme purification, immobilization and its application in biodiesel production.

机构信息

Microbial Chemistry Department, Genetic Engineering and Biotechnology Research Division, National Research Centre, Giza, Egypt.

Microbiology Department, Faculty of Science, Ain Shams University, Abbaseyya, Egypt.

出版信息

Prep Biochem Biotechnol. 2021;51(3):225-240. doi: 10.1080/10826068.2020.1805759. Epub 2020 Aug 18.

DOI:10.1080/10826068.2020.1805759
PMID:32808876
Abstract

The influences of nutritional components affecting lipase production from the new using wheat bran as substrate were studied by employing Plackett-Burman and central composite statistical designs. Out of the 11 medium components tested, sucrose, KHPO and MgSO at final concentrations of 3.0, 1.0 and 0.5 g/L, respectively, were reported to contribute positively to enzyme production (20.09 ± 0.98 U/g ds). The enzyme was purified through ammonium sulfate precipitation followed by Sephadex G-100 gel filtration. Molecular mass of the purified lipase was 57 kDa as evident on SDS-PAGE. Different methods of immobilization were studied and the highest immobilization yield of 81.7 ± 2.18% was reported with agarose (2%) and the optimum temperature was raised from 45 to 50 °C. Immobilized lipase could retain 80% of its original activity at 60 °C after 1 hr of incubation, and was stable at pH values between neutral and alkaline pH. Lipase-catalyzed transesterification process of fungal oil resulted in a fatty acid methyl ester yield consisting of a high percentage of polyunsaturated fatty acids (83.6%), making it appropriate to be used as winter-grade biodiesel. The operational stability studies revealed that the immobilized lipase could keep 70% of its total activity after 5 cycles of the transesterification process.

摘要

以麦麸为底物,利用 Plackett-Burman 和中心组合统计设计研究了影响脂肪酶生产的营养成分的影响。在所测试的 11 种培养基成分中,蔗糖、KHPO 和 MgSO 的最终浓度分别为 3.0、1.0 和 0.5 g/L,被报道对酶生产有积极影响(20.09±0.98 U/g ds)。该酶通过硫酸铵沉淀后再通过 Sephadex G-100 凝胶过滤进行纯化。SDS-PAGE 显示纯化脂肪酶的分子量为 57 kDa。研究了不同的固定化方法,琼脂糖(2%)的固定化产率最高,为 81.7±2.18%,最适温度从 45°C 提高到 50°C。固定化脂肪酶在 60°C 孵育 1 小时后,仍保留其原始活性的 80%,在中性和碱性 pH 值之间稳定。真菌油的脂肪酶催化的酯交换过程导致脂肪酸甲酯的产率含有高比例的多不饱和脂肪酸(83.6%),适合用作冬季级生物柴油。操作稳定性研究表明,固定化脂肪酶在 5 次酯交换过程后仍能保持其总活性的 70%。

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