• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

YD01 对肌苷和鸟苷的生物降解作用

Biodegradation of Inosine and Guanosine by YD01.

机构信息

School of Chemistry and Biological Engineering, University of Science and Technology Beijing, Beijing 100083, China.

出版信息

Int J Mol Sci. 2023 Sep 23;24(19):14462. doi: 10.3390/ijms241914462.

DOI:10.3390/ijms241914462
PMID:37833910
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10573016/
Abstract

Both inosine and guanosine are precursors of uric acid that may cause the diseases of hyperuricemia and gout in humans. Here, a promising bacterial strain for efficiently biodegrading both inosine and guanosine was successfully isolated from a healthy human intestine and identified as YD01 with 16S rRNA analysis. An initial amount of 49.6 mg·L of inosine or 49.9 mg·L of guanosine was completely removed by YD01 within 12 h, which showed that YD01 had a strong ability to biodegrade inosine and guanosine. Furthermore, the initial amount of 49.2 mg·L of inosine or 49.5 mg·L of guanosine was totally catalyzed by the intracellular crude enzymes of YD01 within 6 h, and the initial inosine amount of 49.6 mg·L or guanosine of 49.7 mg·L was biodegraded by the extracellular crude enzymes of YD01 within 9 h. Illumina Hiseq sequencing and database gene annotation were used to elucidate the genomic characteristics of YD01. Purine nucleoside phosphorylase, encoded by gene 1785, gene 3933, and gene 4403, was found in the KEEG database, which played a crucial role in the biodegradation of inosine and guanosine. The results of this study provide valuable insights into the mechanisms for biodegrading inosine and guanosine using YD01.

摘要

肌苷和鸟苷都是尿酸的前体,可能导致人类高尿酸血症和痛风等疾病。在这里,我们从健康人体肠道中成功分离到一株具有高效降解肌苷和鸟苷能力的细菌菌株,并将其鉴定为 YD01,通过 16S rRNA 分析。YD01 在 12 小时内可完全去除 49.6mg·L 的肌苷或 49.9mg·L 的鸟苷,这表明 YD01 具有很强的降解肌苷和鸟苷的能力。此外,YD01 细胞内粗酶在 6 小时内可完全催化 49.2mg·L 的肌苷或 49.5mg·L 的鸟苷,YD01 细胞外粗酶在 9 小时内可完全降解 49.6mg·L 的肌苷或 49.7mg·L 的鸟苷。Illumina Hiseq 测序和数据库基因注释用于阐明 YD01 的基因组特征。在 KEEG 数据库中发现,编码嘌呤核苷磷酸化酶的基因 1785、基因 3933 和基因 4403 发挥了关键作用,可促进肌苷和鸟苷的生物降解。本研究结果为利用 YD01 降解肌苷和鸟苷的机制提供了有价值的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd12/10573016/07ccfc9ea0e9/ijms-24-14462-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd12/10573016/efdcb9b6e686/ijms-24-14462-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd12/10573016/b64ae9c9ee5f/ijms-24-14462-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd12/10573016/6f781c3926bb/ijms-24-14462-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd12/10573016/5929f4cb69ae/ijms-24-14462-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd12/10573016/8b793a8b9916/ijms-24-14462-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd12/10573016/2f65b31a56e2/ijms-24-14462-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd12/10573016/fb9b9e6027e7/ijms-24-14462-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd12/10573016/d7b2663c2a80/ijms-24-14462-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd12/10573016/3a2ea7091209/ijms-24-14462-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd12/10573016/95f1ce9ede58/ijms-24-14462-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd12/10573016/d22420315c6f/ijms-24-14462-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd12/10573016/07ccfc9ea0e9/ijms-24-14462-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd12/10573016/efdcb9b6e686/ijms-24-14462-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd12/10573016/b64ae9c9ee5f/ijms-24-14462-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd12/10573016/6f781c3926bb/ijms-24-14462-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd12/10573016/5929f4cb69ae/ijms-24-14462-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd12/10573016/8b793a8b9916/ijms-24-14462-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd12/10573016/2f65b31a56e2/ijms-24-14462-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd12/10573016/fb9b9e6027e7/ijms-24-14462-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd12/10573016/d7b2663c2a80/ijms-24-14462-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd12/10573016/3a2ea7091209/ijms-24-14462-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd12/10573016/95f1ce9ede58/ijms-24-14462-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd12/10573016/d22420315c6f/ijms-24-14462-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd12/10573016/07ccfc9ea0e9/ijms-24-14462-g012.jpg

相似文献

1
Biodegradation of Inosine and Guanosine by YD01.YD01 对肌苷和鸟苷的生物降解作用
Int J Mol Sci. 2023 Sep 23;24(19):14462. doi: 10.3390/ijms241914462.
2
Incorporation of purine nucleosides in cultured fibroblasts from a patient with purine nucleoside phosphorylase deficiency and associated T-cell immunodeficiency.嘌呤核苷磷酸化酶缺乏及相关T细胞免疫缺陷患者培养成纤维细胞中嘌呤核苷的掺入。
J Cell Physiol. 1977 Jul;92(1):109-13. doi: 10.1002/jcp.1040920113.
3
Profiles of purine biosynthesis, salvage and degradation in disks of potato (Solanum tuberosum L.) tubers.马铃薯(Solanum tuberosum L.)块茎圆盘内嘌呤生物合成、补救途径及降解的概况
Planta. 2006 Dec;225(1):115-26. doi: 10.1007/s00425-006-0334-9. Epub 2006 Jul 15.
4
Biodegradation of Uric Acid by -YC02.-YC02对尿酸的生物降解作用
Microorganisms. 2023 Aug 2;11(8):1989. doi: 10.3390/microorganisms11081989.
5
Purine metabolism in Neisseria meningitidis. 2. Utilization of exogenous adenosine, guanosine and inosine.脑膜炎奈瑟菌中的嘌呤代谢。2. 外源性腺苷、鸟苷和肌苷的利用
Acta Pathol Microbiol Scand B Microbiol Immunol. 1974 Dec;82(6):885-94.
6
[Role of adenine nucleotides in regulating utilization of purine ribonucleosides by Escherichia coli K-12 mutants defective in purine nucleoside phosphorylase].[腺嘌呤核苷酸在调节嘌呤核苷磷酸化酶缺陷的大肠杆菌K-12突变体对嘌呤核糖核苷利用中的作用]
Genetika. 1973 Dec;9(12):102-11.
7
Computer Simulations Reveal Substrate Specificity of Glycosidic Bond Cleavage in Native and Mutant Human Purine Nucleoside Phosphorylase.计算机模拟揭示天然及突变型人嘌呤核苷磷酸化酶中糖苷键裂解的底物特异性。
Biochemistry. 2016 Apr 12;55(14):2153-62. doi: 10.1021/acs.biochem.5b01347. Epub 2016 Mar 29.
8
Screening and application of purine degrading Limosilactobacillus fermentum LF-1 from Huangjiu fermentation broth.从黄酒发酵液中筛选及应用降解嘌呤的发酵乳杆菌LF-1
J Sci Food Agric. 2023 Dec;103(15):7921-7931. doi: 10.1002/jsfa.12881. Epub 2023 Aug 4.
9
Diagnosis of immunodeficiency caused by a purine nucleoside phosphorylase defect by using tandem mass spectrometry on dried blood spots.采用串联质谱法对干血斑进行检测,诊断由嘌呤核苷磷酸化酶缺陷引起的免疫缺陷。
J Allergy Clin Immunol. 2014 Jul;134(1):155-9. doi: 10.1016/j.jaci.2014.01.040. Epub 2014 Apr 24.
10
Screening and characterization of purine nucleoside degrading lactic acid bacteria isolated from Chinese sauerkraut and evaluation of the serum uric acid lowering effect in hyperuricemic rats.从中国酸菜中分离的嘌呤核苷降解乳酸菌的筛选、鉴定及其对高尿酸血症大鼠血清尿酸降低作用的评价
PLoS One. 2014 Sep 3;9(9):e105577. doi: 10.1371/journal.pone.0105577. eCollection 2014.

引用本文的文献

1
Biodegradation of Cholesterol by YS01 Isolated from the Gut of Healthy Individuals.从健康个体肠道中分离出的YS01对胆固醇的生物降解作用。
Microorganisms. 2025 Jun 22;13(7):1451. doi: 10.3390/microorganisms13071451.
2
From Isolation to Pilot-Scale Production: YC07 with Urate-Lowering Potential from Fermented Food Jiangshui.从分离到中试规模生产:来自发酵食品江水的具有降尿酸潜力的YC07
Foods. 2025 Jun 12;14(12):2076. doi: 10.3390/foods14122076.
3
Whole-genome analysis of Bacillus paranthracis YC06 isolated from healthy individual feces for biodegrading inosine and guanosine.

本文引用的文献

1
Purine Metabolism Dysfunctions: Experimental Methods of Detection and Diagnostic Potential.嘌呤代谢功能紊乱:检测方法的实验研究与诊断潜能。
Int J Mol Sci. 2023 Apr 10;24(8):7027. doi: 10.3390/ijms24087027.
2
Design, synthesis, and biological studies of dual URAT1 inhibitor and FXR agonist based on benzbromarone.基于苯溴马隆的双 URAT1 抑制剂和 FXR 激动剂的设计、合成及生物学研究。
Bioorg Med Chem. 2022 Dec 1;75:117073. doi: 10.1016/j.bmc.2022.117073. Epub 2022 Nov 2.
3
Probiotic effects of 1155 and 2644 on hyperuricemic rats.1155和2644对高尿酸血症大鼠的益生菌作用。
从健康个体粪便中分离的副炭疽芽孢杆菌YC06用于生物降解肌苷和鸟苷的全基因组分析。
BMC Microbiol. 2025 May 28;25(1):335. doi: 10.1186/s12866-025-04063-8.
4
Genome Analysis and In Vitro Assay of Probiotic Properties of YC03 with Urate-Lowering Potential.具有降尿酸潜力的YC03益生菌特性的基因组分析及体外测定
Microorganisms. 2025 Mar 31;13(4):798. doi: 10.3390/microorganisms13040798.
5
Evaluating renal injury characteristics in different rat models of hyperuricemia and elucidating pathological molecular mechanisms via serum metabolomics.评估不同高尿酸血症大鼠模型中的肾损伤特征,并通过血清代谢组学阐明其病理分子机制。
Front Pharmacol. 2024 Sep 2;15:1433991. doi: 10.3389/fphar.2024.1433991. eCollection 2024.
6
Exploring the Genomic Landscape of PUMB_17 as a Proficient Phosphatidylcholine-Specific Phospholipase C Producer.探索作为高效磷脂酰胆碱特异性磷脂酶C生产者的PUMB_17的基因组格局。
Curr Issues Mol Biol. 2024 Mar 14;46(3):2497-2513. doi: 10.3390/cimb46030158.
Front Nutr. 2022 Sep 30;9:993951. doi: 10.3389/fnut.2022.993951. eCollection 2022.
4
Gout associated with reduced renal excretion of uric acid. Renal tubular disorder that nephrologists do not treat.与尿酸排泄减少相关的痛风。肾内科医生不治疗的肾小管疾病。
Nefrologia (Engl Ed). 2022 May-Jun;42(3):273-279. doi: 10.1016/j.nefroe.2022.05.007. Epub 2022 Jun 3.
5
Gout and Diet: A Comprehensive Review of Mechanisms and Management.痛风与饮食:机制与管理的全面综述。
Nutrients. 2022 Aug 26;14(17):3525. doi: 10.3390/nu14173525.
6
X11 Ameliorates Hyperuricemia and Modulates Gut Microbiota in Mice.X11 可改善小鼠的高尿酸血症并调节其肠道微生物群。
Front Immunol. 2022 Jul 6;13:940228. doi: 10.3389/fimmu.2022.940228. eCollection 2022.
7
Genomic Analysis of sp. USTB-05 for Biodegrading Cyanobacterial Hepatotoxins.USTB-05 菌的基因组分析及其对蓝藻肝毒素的生物降解作用。
Toxins (Basel). 2022 May 9;14(5):333. doi: 10.3390/toxins14050333.
8
Uric Acid and Oxidative Stress-Relationship with Cardiovascular, Metabolic, and Renal Impairment.尿酸与氧化应激——与心血管、代谢和肾脏损害的关系。
Int J Mol Sci. 2022 Mar 16;23(6):3188. doi: 10.3390/ijms23063188.
9
The potential of probiotics in the amelioration of hyperuricemia.益生菌在改善高尿酸血症中的潜力。
Food Funct. 2022 Mar 7;13(5):2394-2414. doi: 10.1039/d1fo03206b.
10
Genome and Analysis of the Probiotic Properties of a Bacterial Endophyte, Strain MHSD3.细菌内生菌MHSD3的基因组及其益生菌特性分析
Front Genet. 2021 Nov 11;12:672149. doi: 10.3389/fgene.2021.672149. eCollection 2021.