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阐明驱动酶活性的非共价相互作用指导支链酶工程以修饰α-葡聚糖。

Elucidation of the noncovalent interactions driving enzyme activity guides branching enzyme engineering for α-glucan modification.

机构信息

National Engineering Research Center of Industrial Enzymes, Tianjin Institute of Industrial Biotechnology, Chinese Academy of Sciences, Tianjin, China.

National Center of Technology Innovation for Synthetic Biology, Tianjin, China.

出版信息

Nat Commun. 2024 Oct 9;15(1):8760. doi: 10.1038/s41467-024-53018-6.

Abstract

Branching enzymes (BEs) confer to α-glucans, the primary energy-storage reservoir in nature, a variety of features, like slow digestion. The full catalytic cycle of BEs can be divided in six steps, namely two covalent catalytic steps involving glycosylation and transglycosylation, and four noncatalytic steps involving substrate binding and transfers (SBTs). Despite the ever-growing wealth of biochemical and structural information on BEs, clear mechanistic insights into SBTs from an industrial-performance perspective are still missing. Here, we report a Rhodothermus profundi BE (RpBE) endowed with twice as much enzymatic activity as the Rhodothermus obamensis BE currently used in industry. Furthermore, we focus on the SBTs for RpBE by means of large-scale computations supported by experiment. Engineering of the crucial positions responsible for the initial substrate-binding step improves enzymatic activity significantly, while offering a possibility to customize product types. In addition, we show that the high-efficiency substrate-transfer steps preceding glycosylation and transglycosylation are the main reason for the remarkable enzymatic activity of RpBE, suggestive of engineering directions for the BE family.

摘要

支链酶(BEs)赋予α-葡聚糖(自然界中主要的储能库)多种特性,如消化缓慢。BEs 的完整催化循环可分为六个步骤,即涉及糖基化和转糖基化的两个共价催化步骤,以及涉及底物结合和转移(SBTs)的四个非催化步骤。尽管关于 BEs 的生物化学和结构信息不断丰富,但从工业性能的角度来看,对 SBTs 的明确机制见解仍然缺乏。在这里,我们报告了一种富含支链酶的 Rhodothermus profundi(RpBE),其酶活性是目前工业中使用的 Rhodothermus obamensis BE 的两倍。此外,我们通过大规模计算和实验,重点研究了 RpBE 的 SBTs。对负责初始底物结合步骤的关键位置进行工程改造,可显著提高酶活性,同时为定制产品类型提供了可能性。此外,我们还表明,糖基化和转糖基化之前的高效底物转移步骤是 RpBE 具有显著酶活性的主要原因,这为 BE 家族的工程改造提供了方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb51/11464733/3070135c8588/41467_2024_53018_Fig1_HTML.jpg

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