Queiroz Sarah S, Campos Isabela S, Silva Tatiane F, Felipe Maria das Graças A
Department of Biotechnology, Engineering School of Lorena, University of São Paulo, Lorena, São Paulo, 12602-810, Brazil.
Braz J Microbiol. 2025 Mar;56(1):105-116. doi: 10.1007/s42770-024-01564-y. Epub 2024 Nov 19.
Xylitol is a highly demanded polyol in the food, pharmaceutical, and chemical industries. However, its current production methods are considered energy-intensive, require the use of hazardous chemical catalysts, and depend on complex and costly equipment. The biotechnological route of xylitol production is proposed as a sustainable alternative, but it still requires process improvements, such as enhanced fermentation capabilities, to be economically competitive. This study examined Candida tropicalis yeast to improve xylose-to-xylitol conversion via glucose: xylose ratio and pH modulation. Key parameters evaluated included xylose consumption rate (r), xylose-to-xylitol yield (Y), and xylitol volumetric productivity (Q). Conditions with 50 g/L xylose at pH 3.5 exhibited superior xylitol production: 29.81 g/L, Q of 0.52 g/L/h, and Y of 0.54 g/g at 48 h. The statistical model demonstrated that the maximum Y and Q values have not yet been achieved. This could present an opportunity to be explored through yeast genetic engineering approaches. Additionally, the quantitative expression of the xylose transporter genes (XUT1 and STL2) and the xylose reductase gene (XYL1), previously identified in C. tropicalis, was evaluated under all tested conditions. Upregulation of the XUT1 was correlated with higher xylose concentrations, while STL2 was favored at lower xylose concentrations. The expression of XYL1 showed upregulation over time with higher xylose ratios. The high transcription levels and expression profile suggest that Xut1p-mediated xylose transport occurs through a proton symport mechanism. The results indicate that the pH factor indirectly influences XUT1 gene transcription, possibly as a compensatory response to the reduced transporter efficiency under high pH conditions. The present work underscores the influence of glucose ratios and pH in xylitol production, as well as the gene expression of xylose transporters and the key enzyme xylose reductase. Leveraging these insights can significantly enhance xylitol production from hemicellulosic hydrolysates through biotechnological pathways.
木糖醇是食品、制药和化工行业中一种需求旺盛的多元醇。然而,其目前的生产方法被认为能耗高,需要使用危险的化学催化剂,并且依赖于复杂且昂贵的设备。提出了木糖醇生产的生物技术路线作为一种可持续的替代方案,但它仍需要改进工艺,例如提高发酵能力,以具备经济竞争力。本研究考察了热带假丝酵母,通过调节葡萄糖与木糖的比例和pH值来提高木糖向木糖醇的转化率。评估的关键参数包括木糖消耗速率(r)、木糖向木糖醇的产率(Y)和木糖醇体积生产力(Q)。在pH 3.5条件下含有50 g/L木糖的条件显示出优异的木糖醇产量:48小时时为29.81 g/L,Q为0.52 g/L/h,Y为0.54 g/g。统计模型表明尚未达到最大的Y和Q值。这可能为通过酵母基因工程方法探索提供一个机会。此外,在所有测试条件下评估了先前在热带假丝酵母中鉴定出的木糖转运蛋白基因(XUT1和STL2)和木糖还原酶基因(XYL1)的定量表达。XUT1的上调与较高的木糖浓度相关,而STL2在较低木糖浓度下更有利。XYL1的表达随时间和较高的木糖比例而上调。高转录水平和表达谱表明Xut1p介导的木糖转运通过质子同向转运机制发生。结果表明pH因子间接影响XUT1基因转录,可能是对高pH条件下转运蛋白效率降低的一种补偿反应。目前的工作强调了葡萄糖比例和pH对木糖醇生产的影响,以及木糖转运蛋白和关键酶木糖还原酶的基因表达。利用这些见解可以通过生物技术途径显著提高半纤维素水解产物中木糖醇的产量。