The Key Laboratory of Industrial Biotechnology, Ministry of Education, School of Biotechnology, Jiangnan University, Wuxi, Jiangsu 214122, China; Institute of Future Food Technology, JITRI, Yixing 214200, China.
The Key Laboratory of Industrial Biotechnology, Ministry of Education, School of Biotechnology, Jiangnan University, Wuxi, Jiangsu 214122, China.
Bioresour Technol. 2024 Sep;408:131188. doi: 10.1016/j.biortech.2024.131188. Epub 2024 Jul 30.
Currently, fructooligosaccharides (FOS) are converted from sucrose by purified enzymes or fungal cells, but these methods are costly and time-consuming. Here, the optimal fermentation conditions for strain E326 were determined through fermentation optimization: initial glucose 200 g/L, NaCl 25 g/L, inoculum volume 20 %, dissolved oxygen 20-30 %, pH 3, and glucose feeding concentration 100 g/L, which increased erythritol titer by 1.5 times. The co-expression of HGT1 and APC11 genes alleviated the erythritol synthesis stagnation, shorten the fermentation time by 16.7 %, and increased the erythritol productivity by 17.2 %. The episomal plasmids based on yeast mitochondrial replication origins (mtORIs) were constructed to surface display fructosyltransferase, effectively utilizing waste yeast cells generated during erythritol fermentation. Under the conditions of 60℃ and pH 6, the FOS yield reached 65 %, which to our best of knowledge is so-far the highest yield of FOS obtained. These findings will contribute to the industrial production of erythritol and FOS.
目前,果寡糖(FOS)是通过纯化酶或真菌细胞从蔗糖转化而来的,但这些方法成本高且耗时。在这里,通过发酵优化确定了菌株 E326 的最佳发酵条件:初始葡萄糖 200 g/L、NaCl 25 g/L、接种量 20%、溶解氧 20-30%、pH 3 和 100 g/L 的葡萄糖补料浓度,这将赤藓糖醇的产量提高了 1.5 倍。共表达 HGT1 和 APC11 基因缓解了赤藓糖醇合成停滞,使发酵时间缩短了 16.7%,赤藓糖醇生产率提高了 17.2%。构建了基于酵母线粒体复制起点(mtORIs)的附加体质粒,用于表面展示果糖基转移酶,有效利用赤藓糖醇发酵过程中产生的废酵母细胞。在 60℃和 pH 6 的条件下,FOS 的产率达到 65%,据我们所知,这是迄今为止获得的 FOS 的最高产率。这些发现将有助于赤藓糖醇和 FOS 的工业生产。