Aug 2026· Journal of Agricultural and Food Chemistry· Vol 74 35, pp.
27698-27710
· 0 citations· 45 references
Medicine
TL;DR
The identified novel temperature-responsive promoter, PycgM, is a robust, high-temperature genetic element for efficient enzyme and metabolite production in thermotolerant hosts, demonstrating excellent compatibility with a thermotolerant host.
Abstract
As a thermotolerant bacterium, Bacillus licheniformis is an attractive chassis for high-temperature biomanufacturing. Here, we identified a novel temperature-responsive promoter, PycgM, which maintained strong transcriptional activity at 37-52 °C. In a promoter-mCherry reporter system, PycgM exhibited 2287.3-fold higher activity than P2 at 52 °C, demonstrating excellent compatibility with a thermotolerant host. Truncation analysis identified a 150-bp core functional region responsible for optimal activity under induction and heat stress. When applied to drive glutamate decarboxylase expression at 50 °C, PycgM enabled γ-aminobutyric acid production of 391.67 g/L with a 98.69% conversion rate, representing a 275% increase over 37 °C fermentation. The whole-cell biocatalyst retained 86% activity after five reuse cycles, and SEM analysis indicated acceptable structural stability despite moderate morphological changes. These results demonstrate that PycgM is a robust, high-temperature genetic element for efficient enzyme and metabolite production in thermotolerant hosts.
Nitrile hydratase is a key enzyme for nitrile-to-amide hydration under mild conditions, yet its application is limited by low heterologous expression, poor solubility, and suboptimal catalysis. Here, we present an integrated strategy to enhance expression, assembly, and function of Pseudonocardia thermophila NHase (PtN...
Xiao-Lin You, Yu-Qing Chen, Zi-Ying Tan et al.· International Journal of Bio...· 0 citations
The phytopathogenic fungus Chrysoporthe cubensis was cultivated on agro-industrial residues to evaluate laccase production, with coffee husks inducing the highest activity. The enzyme, identified as laccase MCO12, was purified and biochemically characterized, showing acidic activity (pH 2.2-5.0), optimum at 55 °C, and...
Riziane Ferreira Gomes, Rafaela Inês de Souza Ladeira Ázar, Rafaela Zandonade Ventorim et al.· Protein Expression and Purif...· 0 citations
The biochemical characterization and crystal structure of Ta0887, a novel esterase from the thermoacidophilic archaeon Thermoplasma acidophilum, provide a basis for the future engineering of Ta0887 with the aim of enhancing its potential for industrial and biotechnological applications.
Alejandro Delgado-Rey, M. L. Llamas-García, G. Montero-Morán et al.· FEBS Open Bio· 0 citations
Deoxynivalenol (DON), a trichothecene mycotoxin commonly found in cereal grains and their derived products, poses significant risks to human and animal health. In previous work, a fusion enzyme composed of the dehydrogenase DADH and the aldo-keto reductase AKR13B3 was engineered to convert DON into the non-toxic 3-epi-...
Yi-Ting Pan, Hao Zhu, Qing-Wei Jiang et al.· International Journal of Mol...· 0 citations
Keratinases are specialized proteases capable of degrading recalcitrant keratin and have attracted considerable interest for environmentally sustainable bioprocessing. In this study, a keratinase gene from Bacillus tequilensis strain YIV, isolated from tannery waste in Kasur, Pakistan, was cloned, expressed, and charac...
Noor e Hira, I. Haq, M. Aftab· International Journal of Bio...· 0 citations
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