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肌醇转运蛋白IolT1和IolT2促进谷氨酸棒杆菌中由D-果糖生成D-甘露醇。

Myo-inositol facilitators IolT1 and IolT2 enhance D-mannitol formation from D-fructose in Corynebacterium glutamicum.

作者信息

Bäumchen Carsten, Krings Eva, Bringer Stephanie, Eggeling Lothar, Sahm Hermann

机构信息

Institut für Biotechnologie, Forschungszentrum Jülich GmbH, Jülich, Germany.

出版信息

FEMS Microbiol Lett. 2009 Jan;290(2):227-35. doi: 10.1111/j.1574-6968.2008.01425.x. Epub 2008 Nov 20.

Abstract

Reduction of D-fructose to D-mannitol by whole-cell biotransformation with recombinant resting cells of Corynebacterium glutamicum ATCC13032 requires the coexpression of mdh and fdh, which encode mannitol and formate dehydrogenases, respectively. However, d-mannitol formation is limited by the uptake of d-fructose in its unphosphorylated form, because additional expression of the sugar facilitator from Zymomonas mobilis resulted in a significantly increased productivity. Here we identified similarities of the myo-inositol transporters IolT1 and IolT2 of C. glutamicum to the sugar facilitator of Z. mobilis. The myo-inositol transporter genes were both individually overexpressed and deleted in recombinants expressing mdh and fdh. Biotransformation experiments showed that the presence and absence, respectively, of IolT1 and IolT2 significantly influenced D-mannitol formation, indicating a D-fructose transport capability of these transporters. For further evidence, a C. glutamicum Delta ptsF mutant unable to grow with D-fructose was complemented with a heterologous fructokinase gene. This resulted in restoration of growth with D-fructose. Using overexpressed iolT1, mdh and fdh, D-mannitol formation obtained with C. glutamicum was 34.2 g L(-1), as opposed to 16 g L(-1) formed by the strain overexpressing only mdh and fdh, showing the suitability of myo-inositol transporters for D-fructose uptake to obtain D-mannitol formation by whole-cell biotransformation with C. glutamicum.

摘要

利用谷氨酸棒杆菌ATCC13032的重组静息细胞通过全细胞生物转化将D-果糖还原为D-甘露醇,需要共表达分别编码甘露醇脱氢酶和甲酸脱氢酶的mdh和fdh。然而,D-甘露醇的形成受到未磷酸化形式的D-果糖摄取的限制,因为来自运动发酵单胞菌的糖转运蛋白的额外表达导致生产率显著提高。在这里,我们确定了谷氨酸棒杆菌的肌醇转运蛋白IolT1和IolT2与运动发酵单胞菌的糖转运蛋白的相似性。肌醇转运蛋白基因在表达mdh和fdh的重组体中分别单独过表达和缺失。生物转化实验表明,IolT1和IolT2的存在和缺失分别显著影响D-甘露醇的形成,表明这些转运蛋白具有D-果糖转运能力。为了进一步证明,用异源果糖激酶基因互补不能利用D-果糖生长的谷氨酸棒杆菌ΔptsF突变体。这导致恢复了利用D-果糖的生长。使用过表达的iolT1、mdh和fdh,谷氨酸棒杆菌获得的D-甘露醇形成量为34.2 g L(-1),而仅过表达mdh和fdh的菌株形成的量为16 g L(-1),这表明肌醇转运蛋白适用于D-果糖摄取,以通过谷氨酸棒杆菌全细胞生物转化获得D-甘露醇形成。

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