Lijing Chang , Huijuan Cui , Fei Li , Yi-Heng P. Job Zhang , Lingling Zhang
{"title":"通过 ATP 酶再生 ATP,实现体外生物转化","authors":"Lijing Chang , Huijuan Cui , Fei Li , Yi-Heng P. Job Zhang , Lingling Zhang","doi":"10.1016/j.biotechadv.2024.108377","DOIUrl":null,"url":null,"abstract":"<div><p>Adenosine triphosphate (ATP) regeneration is a significant step in both living cells and <em>in vitro</em> biotransformation (<em>iv</em>BT). Rotary motor ATP synthases (ATPases), which regenerate ATP in living cells, have been widely assembled in biomimetic structures for <em>in vitro</em> ATP synthesis. In this review, we present a comprehensive overview of ATPases, including the working principle, orientation and distribution density properties of ATPases, as well as the assembly strategies and applications of ATPase-based ATP regeneration modules. The original sources of ATPases for <em>in vitro</em> ATP regeneration include chromatophores, chloroplasts, mitochondria, and inverted <em>Escherichia coli</em> (<em>E. coli</em>) vesicles, which are readily accessible but unstable. Although significant advances have been made in the assembly methods for ATPase-artificial membranes in recent decades, it remains challenging to replicate the high density and orientation of ATPases observed <em>in vivo</em> using <em>in vitro</em> assembly methods. The use of bioproton pumps or chemicals for constructing proton motive forces (PMF) enables the versatility and potential of ATPase-based ATP regeneration modules. Additionally, overall robustness can be achieved <em>via</em> membrane component selection, such as polymers offering great mechanical stability, or by constructing a solid supporting matrix through layer-by-layer assembly techniques. Finally, the prospects of ATPase-based ATP regeneration modules can be expected with the technological development of ATPases and artificial membranes.</p></div>","PeriodicalId":8946,"journal":{"name":"Biotechnology advances","volume":"73 ","pages":"Article 108377"},"PeriodicalIF":12.1000,"publicationDate":"2024-05-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"ATP regeneration by ATPases for in vitro biotransformation\",\"authors\":\"Lijing Chang , Huijuan Cui , Fei Li , Yi-Heng P. Job Zhang , Lingling Zhang\",\"doi\":\"10.1016/j.biotechadv.2024.108377\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Adenosine triphosphate (ATP) regeneration is a significant step in both living cells and <em>in vitro</em> biotransformation (<em>iv</em>BT). Rotary motor ATP synthases (ATPases), which regenerate ATP in living cells, have been widely assembled in biomimetic structures for <em>in vitro</em> ATP synthesis. In this review, we present a comprehensive overview of ATPases, including the working principle, orientation and distribution density properties of ATPases, as well as the assembly strategies and applications of ATPase-based ATP regeneration modules. The original sources of ATPases for <em>in vitro</em> ATP regeneration include chromatophores, chloroplasts, mitochondria, and inverted <em>Escherichia coli</em> (<em>E. coli</em>) vesicles, which are readily accessible but unstable. Although significant advances have been made in the assembly methods for ATPase-artificial membranes in recent decades, it remains challenging to replicate the high density and orientation of ATPases observed <em>in vivo</em> using <em>in vitro</em> assembly methods. The use of bioproton pumps or chemicals for constructing proton motive forces (PMF) enables the versatility and potential of ATPase-based ATP regeneration modules. Additionally, overall robustness can be achieved <em>via</em> membrane component selection, such as polymers offering great mechanical stability, or by constructing a solid supporting matrix through layer-by-layer assembly techniques. Finally, the prospects of ATPase-based ATP regeneration modules can be expected with the technological development of ATPases and artificial membranes.</p></div>\",\"PeriodicalId\":8946,\"journal\":{\"name\":\"Biotechnology advances\",\"volume\":\"73 \",\"pages\":\"Article 108377\"},\"PeriodicalIF\":12.1000,\"publicationDate\":\"2024-05-17\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Biotechnology advances\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0734975024000715\",\"RegionNum\":1,\"RegionCategory\":\"工程技术\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"BIOTECHNOLOGY & APPLIED MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biotechnology advances","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0734975024000715","RegionNum":1,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0
摘要
三磷酸腺苷(ATP)再生是活细胞和体外生物转化(ivBT)的重要步骤。旋转马达 ATP 合成酶(ATP 酶)可在活细胞中再生 ATP,已被广泛装配到体外 ATP 合成的仿生结构中。在这篇综述中,我们对 ATP 酶进行了全面概述,包括 ATP 酶的工作原理、定向和分布密度特性,以及基于 ATP 酶的 ATP 再生模块的组装策略和应用。体外 ATP 再生 ATP 酶的原始来源包括色素体、叶绿体、线粒体和倒置的大肠杆菌(E. coli)囊泡,这些来源容易获得但不稳定。尽管近几十年来 ATP 酶人工膜的组装方法取得了重大进展,但使用体外组装方法复制体内观察到的 ATP 酶的高密度和定向仍然具有挑战性。使用生物质子泵或化学物质来构建质子动力(PMF),可以实现基于 ATP 酶的 ATP 再生模块的多功能性和潜力。此外,还可以通过选择膜组件(如具有高机械稳定性的聚合物)或通过逐层组装技术构建固体支撑基质来实现整体稳健性。最后,随着 ATP 酶和人工膜技术的发展,基于 ATP 酶的 ATP 再生模块前景可期。
ATP regeneration by ATPases for in vitro biotransformation
Adenosine triphosphate (ATP) regeneration is a significant step in both living cells and in vitro biotransformation (ivBT). Rotary motor ATP synthases (ATPases), which regenerate ATP in living cells, have been widely assembled in biomimetic structures for in vitro ATP synthesis. In this review, we present a comprehensive overview of ATPases, including the working principle, orientation and distribution density properties of ATPases, as well as the assembly strategies and applications of ATPase-based ATP regeneration modules. The original sources of ATPases for in vitro ATP regeneration include chromatophores, chloroplasts, mitochondria, and inverted Escherichia coli (E. coli) vesicles, which are readily accessible but unstable. Although significant advances have been made in the assembly methods for ATPase-artificial membranes in recent decades, it remains challenging to replicate the high density and orientation of ATPases observed in vivo using in vitro assembly methods. The use of bioproton pumps or chemicals for constructing proton motive forces (PMF) enables the versatility and potential of ATPase-based ATP regeneration modules. Additionally, overall robustness can be achieved via membrane component selection, such as polymers offering great mechanical stability, or by constructing a solid supporting matrix through layer-by-layer assembly techniques. Finally, the prospects of ATPase-based ATP regeneration modules can be expected with the technological development of ATPases and artificial membranes.
期刊介绍:
Biotechnology Advances is a comprehensive review journal that covers all aspects of the multidisciplinary field of biotechnology. The journal focuses on biotechnology principles and their applications in various industries, agriculture, medicine, environmental concerns, and regulatory issues. It publishes authoritative articles that highlight current developments and future trends in the field of biotechnology. The journal invites submissions of manuscripts that are relevant and appropriate. It targets a wide audience, including scientists, engineers, students, instructors, researchers, practitioners, managers, governments, and other stakeholders in the field. Additionally, special issues are published based on selected presentations from recent relevant conferences in collaboration with the organizations hosting those conferences.