Nowak Jan Stanislaw, Otzen Daniel E
Interdisciplinary Nanoscience Center (iNANO), Aarhus University, Gustav Wieds Vej 14, DK - 8000 Aarhus C, Denmark.
BBA Adv. 2023 Nov 27;5:100104. doi: 10.1016/j.bbadva.2023.100104. eCollection 2024.
Enzymes from psychrophilic (cold-loving) organisms have attracted considerable interest over the past decades for their potential in various low-temperature industrial processes. However, we still lack large-scale commercialization of their activities. Here, we review their properties, limitations and potential. Our review is structured around answers to 5 central questions: 1. How do cold-active enzymes achieve high catalytic rates at low temperatures? 2. How is protein flexibility connected to cold-activity? 3. What are the sequence-based and structural determinants for cold-activity? 4. How does the thermodynamic stability of psychrophilic enzymes reflect their cold-active capabilities? 5. How do we effectively identify novel cold-active enzymes, and can we apply them in an industrial context? We conclude that emerging screening technologies combined with big-data handling and analysis make it reasonable to expect a bright future for our understanding and exploitation of cold-active enzymes.
在过去几十年里,嗜冷(喜冷)生物的酶因其在各种低温工业过程中的潜力而备受关注。然而,我们仍缺乏对其活性的大规模商业化应用。在此,我们综述了它们的特性、局限性和潜力。我们的综述围绕对5个核心问题的回答展开:1. 冷活性酶如何在低温下实现高催化速率?2. 蛋白质柔韧性与冷活性是如何关联的?3. 冷活性的基于序列和结构的决定因素有哪些?4. 嗜冷酶的热力学稳定性如何反映其冷活性能力?5. 我们如何有效地鉴定新型冷活性酶,以及能否将它们应用于工业环境?我们得出结论,新兴的筛选技术与大数据处理和分析相结合,使我们有理由期待在理解和利用冷活性酶方面拥有光明的未来。