Department of Biological Sciences, St. Edward's University, 3001 S Congress Ave, Austin, TX 78704, USA.
Phaff Yeast Culture Collection, Food Science and Technology, University of California Davis, One Shields Ave, Davis, CA 95616, USA.
J Ind Microbiol Biotechnol. 2024 Jan 9;51. doi: 10.1093/jimb/kuae037.
Fermentation of pectin-rich biomass by Saccharomyces cerevisiae can produce bioethanol as a fuel replacement to combat carbon dioxide emissions from the combustion of fossil fuels. Saccharomyces cerevisiae UCDFST 09-448 produces its own pectinase enzymes potentially eliminating the need for commercial pectinases during fermentation. This research assessed growth, pectinase activity, and fermentative activity of S. cerevisiae UCDFST 09-448 and compared its performance to an industrial yeast strain, S. cerevisiae XR122N. Saccharomyces cerevisiae UCDFST 09-448's growth was inhibited by osmotic stress (xylose concentrations above 1 M), ethanol concentrations greater than 5% v/v, and temperatures outside of 30°C-37°C. However, S. cerevisiae UCDFST 09-448 was able to consistently grow in an industrial pH range (3-6). It was able to metabolize glucose, sucrose, and fructose but was unable to metabolize arabinose, xylose, and galacturonic acid. The pectinase enzyme produced by S. cerevisiae UCDFST 09-448 was active under typical fermentation conditions (35°C-37°C, pH 5.0). Regardless of S. cerevisiae UCDFST 09-448's limitations when compared to S. cerevisiae XR122N in 15% w/v peach fermentations, S. cerevisiae UCDFST 09-448 was still able to achieve maximum ethanol yields in the absence of commercial pectinases (44.7 ± 3.1 g/L). Under the same conditions, S. cerevisiae XR122N produced 39.5 ± 3.1 g/L ethanol. While S. cerevisiae UCDFST 09-448 may not currently be optimized for industrial fermentations, it is a step toward a consolidated bioprocessing approach to fermentation of pectin-rich biomass.
ONE-SENTENCE SUMMARY: Saccharomyces cerevisiae UCDFST 09-448 demonstrates the potential to ferment pectin-rich biomass as part of a consolidated bioprocess, but is sensitive to industrial stressors.
通过酿酒酵母发酵富含果胶的生物质可以生产生物乙醇,作为替代物来对抗化石燃料燃烧产生的二氧化碳排放。酿酒酵母 UCDFST 09-448 自身产生果胶酶,可能在发酵过程中不需要使用商业果胶酶。本研究评估了酿酒酵母 UCDFST 09-448 的生长、果胶酶活性和发酵活性,并将其性能与工业酵母菌株酿酒酵母 XR122N 进行了比较。酿酒酵母 UCDFST 09-448 的生长受到渗透压(木糖浓度高于 1 M)、乙醇浓度大于 5%(体积/体积)和 30°C-37°C 以外温度的抑制。然而,酿酒酵母 UCDFST 09-448 能够始终在工业 pH 范围内(3-6)生长。它能够代谢葡萄糖、蔗糖和果糖,但不能代谢阿拉伯糖、木糖和半乳糖醛酸。酿酒酵母 UCDFST 09-448 产生的果胶酶在典型的发酵条件(35°C-37°C,pH5.0)下具有活性。尽管酿酒酵母 UCDFST 09-448 在 15%(重量/体积)桃发酵中与酿酒酵母 XR122N 相比存在限制,但在没有商业果胶酶的情况下,酿酒酵母 UCDFST 09-448 仍能够达到最大乙醇产量(44.7±3.1 g/L)。在相同条件下,酿酒酵母 XR122N 产生 39.5±3.1 g/L 乙醇。虽然酿酒酵母 UCDFST 09-448 目前可能不适合工业发酵,但它是朝着果胶丰富的生物质发酵的综合生物加工方法迈出的一步。
酿酒酵母 UCDFST 09-448 具有作为综合生物加工的一部分发酵富含果胶的生物质的潜力,但对工业应激物敏感。