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来自[具体来源未给出]的嘌呤核苷磷酸化酶的特性及其在降低啤酒中嘌呤含量方面的潜在应用。

The Characterization of the Purine Nucleoside Phosphorylase from and Its Potential Application in Reducing Purine Content in Beer.

作者信息

Liu Jun, Lu Jian

机构信息

Key Laboratory of Industrial Biotechnology, Ministry of Education, School of Biotechnology, Jiangnan University, Wuxi 214122, China.

National Engineering Research Center of Cereal Fermentation and Food Biomanufacturing, Jiangnan University, Wuxi 214122, China.

出版信息

J Fungi (Basel). 2025 Mar 31;11(4):268. doi: 10.3390/jof11040268.

Abstract

Beer, the most popular alcoholic beverage, poses health risks for individuals with gout and hyperuricemia due to its high purine content. Herein, we identified a novel purine nucleoside phosphorylase (PNP) from the edible mushroom and heterologously expressed it in . The recombinant PNP exhibited optimal activity at 60 °C and pH 7.0, retaining >80% activity at pH 6.0-9.0 and >85% activity after 3 h at ≤60 °C. Kinetic analysis revealed high catalytic efficiency (kcat/Km = 2.02 × 10 s⋅M) toward inosine, with strong resistance to metal ions except for Co and Cu. The application of PNP (1.0-5.0 U/mL) during wort saccharification reduced purine nucleosides by 33.54% (from 151.53 to 100.65 mg/L) while increasing yeast utilization of free purine bases. The resulting beer showed improved fermentation performance (alcohol content increased by 3.6%) without compromising flavor profiles. This study provides the food-grade enzymatic strategy for low-purine beer production, leveraging the GRAS status of both and .

摘要

啤酒是最受欢迎的酒精饮料,因其高嘌呤含量,对痛风和高尿酸血症患者构成健康风险。在此,我们从食用蘑菇中鉴定出一种新型嘌呤核苷磷酸化酶(PNP),并在[具体表达系统]中进行了异源表达。重组PNP在60°C和pH 7.0时表现出最佳活性,在pH 6.0 - 9.0时保留>80%的活性,在≤60°C下3小时后保留>85%的活性。动力学分析表明,其对肌苷具有高催化效率(kcat/Km = 2.02×10 s⋅M),对除Co和Cu以外的金属离子具有较强抗性。在麦芽汁糖化过程中应用PNP(1.0 - 5.0 U/mL)可使嘌呤核苷减少33.54%(从151.53降至100.65 mg/L),同时提高酵母对游离嘌呤碱的利用率。所得啤酒发酵性能得到改善(酒精含量增加3.6%),且风味不受影响。本研究利用[具体菌种]和[具体表达系统]的公认安全(GRAS)地位,为低嘌呤啤酒生产提供了食品级酶策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5beb/12028538/2cf14c3e4a9f/jof-11-00268-g001.jpg

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