Durairaj Pradeepraj, Li Shengying
State Key Laboratory of Microbial Technology, Shandong University, Qingdao 266237, Shandong, China.
Laboratory for Marine Biology and Biotechnology, Qingdao National Laboratory for Marine Science and Technology, Qingdao 266237, Shandong, China.
Eng Microbiol. 2022 Jan 19;2(1):100011. doi: 10.1016/j.engmic.2022.100011. eCollection 2022 Mar.
Cytochrome P450 (CYP) enzymes play crucial roles during the evolution and diversification of ancestral monocellular eukaryotes into multicellular eukaryotic organisms due to their essential functionalities including catalysis of housekeeping biochemical reactions, synthesis of diverse metabolites, detoxification of xenobiotics, and contribution to environmental adaptation. Eukaryotic CYPs with versatile functionalities are undeniably regarded as promising biocatalysts with great potential for biotechnological, pharmaceutical and chemical industry applications. Nevertheless, the modes of action and the challenges associated with these membrane-bound proteins have hampered the effective utilization of eukaryotic CYPs in a broader range. This review is focused on comprehensive and consolidated approaches to address the core challenges in heterologous expression of membrane-bound eukaryotic CYPs in different surrogate microbial cell factories, aiming to provide key insights for better studies and applications of diverse eukaryotic CYPs in the future. We also highlight the functional significance of the previously underrated cytochrome P450 reductases (CPRs) and provide a rational justification on the progression of CPR from auxiliary redox partner to function modulator in CYP catalysis.
细胞色素P450(CYP)酶在祖先单细胞真核生物进化和多样化为多细胞真核生物的过程中发挥着关键作用,这是由于其具有多种重要功能,包括催化看家生化反应、合成多种代谢产物、对外源生物进行解毒以及促进环境适应。具有多种功能的真核生物CYP无疑被视为具有巨大潜力的生物催化剂,在生物技术、制药和化学工业应用中前景广阔。然而,这些膜结合蛋白的作用方式以及与之相关的挑战阻碍了真核生物CYP在更广泛领域的有效利用。本综述聚焦于全面且综合的方法,以应对在不同替代微生物细胞工厂中膜结合真核生物CYP异源表达的核心挑战,旨在为未来更好地研究和应用各种真核生物CYP提供关键见解。我们还强调了此前被低估的细胞色素P450还原酶(CPR)的功能重要性,并对CPR在CYP催化中从辅助氧化还原伙伴向功能调节剂的发展过程提供了合理的解释。