Department of Biotechnology, Indian Institute of Technology Kharagpur, Kharagpur, 721302, India.
Department of Biotechnology, Indian Institute of Technology Kharagpur, Kharagpur, 721302, India.
Arch Biochem Biophys. 2020 Nov 30;695:108645. doi: 10.1016/j.abb.2020.108645. Epub 2020 Oct 22.
Microbial conversion of lignocellulosic feedstock to the target bioproduct requires efficient assimilation of its constituent sugars, a large part of which comprises of glucose and xylose. This study aims to identify and characterize sugar transporters capable of xylose uptake in an oleaginous strain of the industrially relevant yeast Candida tropicalis. In silico database mining resulted in two sugar transporter proteins- CtStp1 and CtStp2, containing conserved amino acid residues and motifs that have been previously reported to be involved in xylose transport in other organisms. Several softwares predicted the likelihood of 10-12 transmembrane (TM) helices to be present in both the Stps, while molecular modelling showed 12 TM helices that were organized into a typical structure found in the major facilitator superfamily of transporters. Docking with different sugars also predicted favorable interactions. Heterologous expression in a Saccharomyces cerevisiae strain harboring functional xylose metabolic genes validated the broad substrate specificity of the two Stps. Each transporter supported prominent growth of recombinant S. cerevisiae strains on six sugars including xylose at various concentrations. Expression of CtSTP1 and CtSTP2 along with the xylose metabolic genes in yeast transformants grown in presence of xylose was confirmed by transcript detection. Growth curve and sugar consumption profiles revealed uptake of both glucose and xylose simultaneously by the recombinant yeast strains, though CtStp1 showed relatively less effect of glucose repression in mixed sugars and was a better transporter of xylose than CtStp2. Such glucose-xylose utilizing efficient transporters can be effective tools for developing co-fermenting yeasts through genetic engineering in future, with noteworthy applications in renewable biomass utilization.
木质纤维素原料的微生物转化为目标生物制品需要有效地同化其组成糖,其中大部分由葡萄糖和木糖组成。本研究旨在鉴定和表征能够在工业相关酵母热带假丝酵母的油脂菌株中吸收木糖的糖转运蛋白。通过计算机数据库挖掘,发现了两种糖转运蛋白 CtStp1 和 CtStp2,它们含有保守的氨基酸残基和基序,这些残基和基序以前曾被报道在其他生物体中参与木糖转运。几种软件预测这两种 Stp 都存在 10-12 个跨膜(TM)螺旋的可能性,而分子建模显示 12 个 TM 螺旋组成了一个在主要易化因子超家族转运蛋白中发现的典型结构。与不同糖的对接也预测了有利的相互作用。在含有功能性木糖代谢基因的酿酒酵母菌株中异源表达,验证了这两种 Stp 的广泛底物特异性。两种转运蛋白都支持重组酿酒酵母菌株在包括木糖在内的六种不同浓度的糖上的显著生长。CtSTP1 和 CtSTP2 的表达以及在存在木糖的酵母转化体中与木糖代谢基因一起表达,通过转录物检测得到证实。生长曲线和糖消耗谱表明,重组酵母菌株同时吸收葡萄糖和木糖,尽管 CtStp1 在混合糖中对葡萄糖抑制的影响相对较小,并且是比 CtStp2 更好的木糖转运蛋白。这种葡萄糖-木糖利用高效转运蛋白可以通过遗传工程在未来成为开发共发酵酵母的有效工具,在可再生生物质利用方面具有重要应用。