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在解脂耶氏酵母中过表达分泌型蔗糖异构酶及其在固定化后生产异麦芽酮糖中的应用。

Overexpression of secreted sucrose isomerase in Yarrowia lipolytica and its application in isomaltulose production after immobilization.

机构信息

Tobacco Research Institute, Chinese Academy of Agricultural Sciences, Qingdao, Shandong 266101, China.

Key Laboratory of Sustainable Development of Polar Fishery, Ministry of Agriculture and Rural Affairs, Yellow Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Qingdao, Shandong 266071, China.

出版信息

Int J Biol Macromol. 2019 Jan;121:97-103. doi: 10.1016/j.ijbiomac.2018.10.010. Epub 2018 Oct 2.

Abstract

Isomaltulose production by bacterial fermentation was limited, due to generation of undesirable products and reduced yields. Isomaltulose production using sucrose isomerase (SIase) catalyzed methods was expected to be more applicable, but was hampered by low SIase activity and lack of a secreted SIase producer. Here, we aimed to obtain high levels of secreted SIase by overexpressing the SIase gene from Pantoea dispersa UQ68J in Yarrowia lipolytica, a successful host for efficient secretory expression, with a newly characterized strong constitutive promoter. After optimization of the culture medium, the engineered strain JD secreted SIase with an activity of 49.3 U/mL. The recombinant SIase was effectively immobilized onto polyvinyl alcohol-alginate, and the enzymatic activity recovery rate was up to 82.4%. The stability of the SIase was significantly improved by immobilization. Batch production of isomaltulose catalyzed by the immobilized SIase was performed under optimal conditions, generating 620.7 g/L isomaltulose with a yield of 0.96 g/g. The conversion rate of sucrose after 13 batches remained above 90%. These results demonstrated that the proposed SIase expression and immobilization method was promising in the industrial production of isomaltulose.

摘要

由于产生不良产物和产量降低,细菌发酵生产异麦芽酮糖受到限制。预计利用蔗糖异构酶(SIase)催化方法生产异麦芽酮糖更适用,但受到低 SIase 活性和缺乏分泌型 SIase 产生菌的限制。本研究旨在通过在产脂肪酵母 Yarrowia lipolytica 中过表达泛菌属 UQ68J 的 SIase 基因,获得高水平的分泌型 SIase,该基因具有新鉴定的强组成型启动子,可实现高效分泌表达。在优化培养基后,工程菌 JD 分泌的 SIase 活性达到 49.3 U/mL。重组 SIase 有效地固定在聚乙烯醇-海藻酸钠上,酶活回收率高达 82.4%。固定化显著提高了 SIase 的稳定性。在最佳条件下,利用固定化 SIase 进行分批生产异麦芽酮糖,生成 620.7 g/L 的异麦芽酮糖,产率为 0.96 g/g。13 批后蔗糖的转化率仍保持在 90%以上。这些结果表明,所提出的 SIase 表达和固定化方法在异麦芽酮糖的工业生产中具有很大的应用潜力。

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