Enhanced deoxyviolacein bioproduction via enzyme condensation with a yeast glycolytic enzyme-derived peptide tag

IF 2.8 3区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Biotechnology Progress Pub Date : 2026-02-16 Epub Date: 2025-10-11 DOI:10.1002/btpr.70079
Rioko Ito, Sayoko Ito-Harashima, Naoko Segawa, Natsuko Miura, Michihiko Kataoka
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引用次数: 0

Abstract

In microbial production, regulating endogenous and exogenous synthetic pathways is essential. Techniques to induce intracellular enzyme condensation have attracted attention as a means to increase apparent enzyme activity with minimal transcriptional and translational burden on the cell. Artificial enzyme condensation can be induced by tagging enzymes with specific proteins or peptides. In our previous study, we identified novel peptide tags derived from condensate-forming Saccharomyces cerevisiae glycolytic enzymes and their potential use in controlling intracellular metabolism by inducing artificial condensates in S. cerevisiae cells. Herein, we evaluated the condensate formation of two enzymes using peptide tags and the branched violacein biosynthetic pathway from Pseudoalteromonas luteoviolacea in S. cerevisiae, and tested the effects of modulating biosynthesis to increase the production of deoxyviolacein, a byproduct with antibacterial and anticancer activities. We used several protein and peptide tags with a simplified expression system, and all the tags successfully induced artificial condensate formation in the cell. Additionally, introducing a short peptide tag successfully increased deoxyviolacein production by approximately twofold, displaying a higher efficacy compared to FUSN, a previously reported N-terminal 213 amino acid region with an intrinsically disordered property. These results demonstrate the potential use of peptide tags to enhance bioproduction through the regulation of endogenous and exogenous synthetic pathways. The methods contribute to the development of novel strategies for microorganisms to be used for bioproduction through the controlled condensation of metabolic enzymes in cells.

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Abstract Image

通过酵母菌糖酵解酶衍生肽标签的酶缩合增强脱氧紫罗兰素的生物生产。
在微生物生产中,调节内源性和外源性合成途径是必不可少的。诱导细胞内酶缩合的技术已经引起了人们的关注,因为它是一种以最小的细胞转录和翻译负担来增加表观酶活性的手段。人工酶缩合可以通过用特定的蛋白质或肽标记酶来诱导。在我们之前的研究中,我们发现了从凝结物形成的酿酒酵母糖酵解酶中衍生的新的肽标签,以及它们在酿酒酵母细胞中通过诱导人工凝聚物控制细胞内代谢的潜在用途。本文研究了酿酒葡萄球菌假异单胞菌(Pseudoalteromonas luteoviolacea)中两种酶的肽标记凝结物形成和支链堇菜素生物合成途径,并测试了调节生物合成以增加脱氧堇菜素(deoxyviolacein)产量的效果,脱氧堇菜素是具有抗菌和抗癌活性的副产物。我们使用了多种蛋白质和肽标签,并建立了一个简化的表达系统,所有的标签都成功地在细胞中诱导了人工凝析物的形成。此外,引入短肽标签成功地将脱氧紫罗兰素的产量提高了约两倍,与先前报道的具有内在无序特性的n端213个氨基酸区域FUSN相比,显示出更高的功效。这些结果证明了肽标签通过调节内源性和外源性合成途径来增强生物生产的潜在用途。这些方法有助于开发新的微生物策略,通过控制细胞中代谢酶的缩合来进行生物生产。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Biotechnology Progress
Biotechnology Progress 工程技术-生物工程与应用微生物
CiteScore
6.50
自引率
3.40%
发文量
83
审稿时长
4 months
期刊介绍: Biotechnology Progress , an official, bimonthly publication of the American Institute of Chemical Engineers and its technological community, the Society for Biological Engineering, features peer-reviewed research articles, reviews, and descriptions of emerging techniques for the development and design of new processes, products, and devices for the biotechnology, biopharmaceutical and bioprocess industries. Widespread interest includes application of biological and engineering principles in fields such as applied cellular physiology and metabolic engineering, biocatalysis and bioreactor design, bioseparations and downstream processing, cell culture and tissue engineering, biosensors and process control, bioinformatics and systems biology, biomaterials and artificial organs, stem cell biology and genetics, and plant biology and food science. Manuscripts concerning the design of related processes, products, or devices are also encouraged. Four types of manuscripts are printed in the Journal: Research Papers, Topical or Review Papers, Letters to the Editor, and R & D Notes.
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