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与乙酰激酶共固定化 RizA 变体以生产生物活性的精氨酰二肽。

Co-Immobilization of RizA Variants with Acetate Kinase for the Production of Bioactive Arginyl Dipeptides.

机构信息

Institut für Lebensmittelchemie, Gottfried Wilhelm Leibniz Universität Hannover, Callinstraße 5, 30167 Hannover, Germany.

出版信息

Molecules. 2022 Jul 7;27(14):4352. doi: 10.3390/molecules27144352.

Abstract

The biocatalytic system comprised of RizA and acetate kinase (AckA) combines the specific synthesis of bioactive arginyl dipeptides with efficient ATP regeneration. Immobilization of this coupled enzyme system was performed and characterized in terms of activity, specificity and reusability of the immobilisates. Co-immobilization of RizA and AckA into a single immobilisate conferred no disadvantage in comparison to immobilization of only RizA, and a small addition of AckA (20:1) was sufficient for ATP regeneration. New variants of RizA were constructed by combining mutations to yield variants with increased biocatalytic activity and specificity. A selection of RizA variants were co-immobilized with AckA and used for the production of the salt-taste enhancers Arg-Ser and Arg-Ala and the antihypertensive Arg-Phe. The best variants yielded final dipeptide concentrations of 11.3 mM Arg-Ser (T81F_A158S) and 11.8 mM Arg-Phe (K83F_S156A), the latter of which represents a five-fold increase in comparison to the wild-type enzyme. T81F_A158S retained more than 50% activity for over 96 h and K83F_S156A for over 72 h. This study provides the first example of the successful co-immobilization of an l-amino acid ligase with an ATP-regenerating enzyme and paves the way towards a bioprocess for the production of bioactive dipeptides.

摘要

该生物催化系统由 RizA 和乙酰激酶(AckA)组成,将生物活性精氨酰二肽的特异性合成与高效的 ATP 再生相结合。对该偶联酶系统进行了固定化,并从固定化产物的活性、特异性和可重复使用性方面进行了表征。与仅固定 RizA 相比,RizA 和 AckA 共固定化没有任何不利影响,并且只需添加少量的 AckA(20:1)即可进行 ATP 再生。通过组合突变构建了 RizA 的新变体,从而产生了具有更高生物催化活性和特异性的变体。选择了一些 RizA 变体与 AckA 共固定化,用于生产盐味增强剂 Arg-Ser 和 Arg-Ala 以及降压肽 Arg-Phe。最佳变体的最终二肽浓度为 11.3 mM Arg-Ser(T81F_A158S)和 11.8 mM Arg-Phe(K83F_S156A),与野生型酶相比,后者提高了五倍。T81F_A158S 在超过 96 小时内保留了超过 50%的活性,而 K83F_S156A 在超过 72 小时内保留了超过 50%的活性。本研究首次成功地将 l-氨基酸连接酶与 ATP 再生酶共固定化,并为生物活性二肽的生产开辟了一条生物工艺途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11ab/9321006/e34b9b94078e/molecules-27-04352-g001.jpg

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