Fortuin Jordan, Hoffmeester Lazzlo J, Minnaar Letitia S, den Haan Riaan
Department of Biotechnology, University of the Western Cape, Bellville, South Africa.
Appl Microbiol Biotechnol. 2025 Feb 13;109(1):43. doi: 10.1007/s00253-025-13426-0.
Despite the lack of implementation of consolidated bioprocessing (CBP) at an industrial scale, this bioconversion strategy still holds significant potential as an economically viable solution for converting lignocellulosic biomass (LCB) into biofuels and green chemicals, provided an appropriate organism can be isolated or engineered. The use of Saccharomyces cerevisiae for this purpose requires, among other things, the development of a cellulase expression system within the yeast. Over the past three decades, numerous studies have reported the expression of cellulase-encoding genes, both individually and in combination, in S. cerevisiae. Various strategies have emerged to produce a core set of cellulases, with differing degrees of success. While one-step conversion of cellulosic substrates to ethanol has been reported, the resulting titers and productivities fall well below industrial requirements. In this review, we examine the strategies employed for cellulase expression in yeast, highlighting the successes in developing basic cellulolytic CBP-enabled yeasts. We also summarize recent advancements in rational strain design and engineering, exploring how these approaches can be further enhanced through modern synthetic biology tools to optimize CBP-enabled yeast strains for potential industrial applications. KEY POINTS: • S. cerevisiae's lack of cellulolytic ability warrants its engineering for industry. • Advancements in the expression of core sets of cellulases have been reported. • Rational engineering is needed to enhance cellulase secretion and strain robustness. • Insights gained from omics strategies will direct the future development of CBP strains.
尽管在工业规模上尚未实施整合生物加工(CBP),但只要能够分离或改造出合适的生物体,这种生物转化策略作为将木质纤维素生物质(LCB)转化为生物燃料和绿色化学品的经济可行解决方案,仍具有巨大潜力。将酿酒酵母用于此目的,除其他外,需要在酵母中开发一种纤维素酶表达系统。在过去三十年中,众多研究报告了纤维素酶编码基因在酿酒酵母中单独或组合表达的情况。已经出现了各种策略来生产一组核心纤维素酶,其成功程度各不相同。虽然已有报道将纤维素底物一步转化为乙醇,但所得的滴度和生产率远低于工业要求。在这篇综述中,我们研究了在酵母中表达纤维素酶所采用的策略,突出了在开发能够实现基本纤维素分解的CBP酵母方面所取得的成功。我们还总结了合理菌株设计和工程方面的最新进展,探讨如何通过现代合成生物学工具进一步加强这些方法,以优化能够实现CBP的酵母菌株,用于潜在的工业应用。要点:• 酿酒酵母缺乏纤维素分解能力,因此需要对其进行工程改造以用于工业生产。• 已有关于核心纤维素酶组表达方面的进展报道。• 需要进行合理工程改造以提高纤维素酶分泌和菌株稳健性。• 从组学策略中获得的见解将指导CBP菌株的未来发展。