• 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

TMG-壳三糖霉素,一种由放线菌环形链霉菌NBRC 13369产生的、对昆虫和真菌β-N-乙酰氨基葡萄糖苷酶具有特异性的酶抑制剂。

TMG-chitotriomycin, an enzyme inhibitor specific for insect and fungal beta-N-acetylglucosaminidases, produced by actinomycete Streptomyces anulatus NBRC 13369.

作者信息

Usuki Hirokazu, Nitoda Teruhiko, Ichikawa Misato, Yamaji Nahoko, Iwashita Takashi, Komura Hajime, Kanzaki Hiroshi

机构信息

Laboratory of Bioresources Chemistry, The Graduate School of Natural Science and Technology, Okayama University, Okayama 700-8530, Japan.

出版信息

J Am Chem Soc. 2008 Mar 26;130(12):4146-52. doi: 10.1021/ja077641f. Epub 2008 Feb 29.

DOI:10.1021/ja077641f
PMID:18307344
Abstract

A novel beta-N-acetylglucosaminidase (GlcNAcase) inhibitor named TMG-chitotriomycin (1) was isolated from the culture filtrate of Streptomyces anulatus NBRC13369. The strain produced 1 only when colloidal chitin was used as the sole carbon source in the production medium. The structure of 1 was determined by spectral and constitutive sugar analyses of the corresponding alditol derivatives to be an equilibrated mixture of alpha-d-N,N,N-triMeGlcNH2-(1,4)-beta-d-GlcNAc-(1,4)-beta-d-GlcNAc-(1,4)-d-GlcNAc and its C-2 epimer of the reducing end residue. TMG-chitotriomycin (1) showed potent and selective inhibition of insect and fungal GlcNAcases with no inhibition of mammalian and plant GlcNAcases. In contrast, the known GlcNAcase inhibitor nagstatin potently inhibited all GlcNAcases. It should be emphasized that synthesized d-N,N,N-triMeGlcNH2, which is the component sugar of 1, showed no inhibition of the insect Spodoptera litura GlcNAcase. These results suggest that the (GlcNAc)3 unit positioned at the reducing end of 1 is essential for its enzyme inhibitory activity. The unique inhibitory spectrum of 1 will be useful to study chitinolytic systems and to develop selective fungicides or pesticides.

摘要

一种名为TMG-壳三糖霉素(1)的新型β-N-乙酰氨基葡萄糖苷酶(GlcNAcase)抑制剂从环状链霉菌NBRC13369的培养滤液中分离得到。该菌株仅在生产培养基中使用胶体几丁质作为唯一碳源时才产生1。通过对相应糖醇衍生物的光谱和组成糖分析确定1的结构为α-d-N,N,N-三甲基葡糖胺-(1,4)-β-d- GlcNAc-(1,4)-β-d- GlcNAc-(1,4)-d- GlcNAc及其还原端残基的C-2差向异构体的平衡混合物。TMG-壳三糖霉素(1)对昆虫和真菌的GlcNAcase表现出强效且选择性的抑制作用,而对哺乳动物和植物的GlcNAcase没有抑制作用。相比之下,已知的GlcNAcase抑制剂纳他汀对所有GlcNAcase都有强效抑制作用。应该强调的是,合成的d-N,N,N-三甲基葡糖胺作为1的组成糖,对昆虫斜纹夜蛾的GlcNAcase没有抑制作用。这些结果表明,位于1还原端的(GlcNAc)3单元对其酶抑制活性至关重要。1独特的抑制谱将有助于研究几丁质分解系统以及开发选择性杀菌剂或杀虫剂。

相似文献

1
TMG-chitotriomycin, an enzyme inhibitor specific for insect and fungal beta-N-acetylglucosaminidases, produced by actinomycete Streptomyces anulatus NBRC 13369.TMG-壳三糖霉素,一种由放线菌环形链霉菌NBRC 13369产生的、对昆虫和真菌β-N-乙酰氨基葡萄糖苷酶具有特异性的酶抑制剂。
J Am Chem Soc. 2008 Mar 26;130(12):4146-52. doi: 10.1021/ja077641f. Epub 2008 Feb 29.
2
Total synthesis and structural revision of TMG-chitotriomycin, a specific inhibitor of insect and fungal beta-N-acetylglucosaminidases.昆虫和真菌β-N-乙酰氨基葡萄糖苷酶的特异性抑制剂TMG-壳三糖霉素的全合成及结构修正
J Am Chem Soc. 2009 Sep 2;131(34):12076-7. doi: 10.1021/ja9055245.
3
Kinetic and thermodynamic insights into the inhibitory mechanism of TMG-chitotriomycin on Vibrio campbellii GH20 exo-β-N-acetylglucosaminidase.动力学和热力学研究表明 TMG-壳三霉素对坎贝尔氏弧菌 GH20 外切-β-N-乙酰氨基葡萄糖苷酶的抑制机制。
Carbohydr Res. 2021 Jan;499:108201. doi: 10.1016/j.carres.2020.108201. Epub 2020 Nov 20.
4
TMG-chitotriomycin as a probe for the prediction of substrate specificity of β-N-acetylhexosaminidases.TMG-壳三糖苷霉素作为一种探针,用于预测β-N-乙酰己糖苷酶的底物特异性。
Carbohydr Res. 2013 Jun 28;375:29-34. doi: 10.1016/j.carres.2013.04.024. Epub 2013 Apr 27.
5
MS/MS fragmentation-guided search of TMG-chitooligomycins and their structure-activity relationship in specific β-N-acetylglucosaminidase inhibition.TMG-壳寡糖菌素的 MS/MS 碎裂引导搜索及其在特定β-N-乙酰氨基葡萄糖苷酶抑制中的构效关系。
Org Biomol Chem. 2011 Apr 21;9(8):2943-51. doi: 10.1039/c0ob01090a. Epub 2011 Mar 4.
6
Synthesis, evaluation, and mechanism of N,N,N-trimethyl-D-glucosamine-(1→4)-chitooligosaccharides as selective inhibitors of glycosyl hydrolase family 20 β-N-acetyl-D-hexosaminidases.N,N,N-三甲基-D-葡萄糖胺-(1→4)-壳寡糖作为糖苷水解酶家族 20β-N-乙酰-D-氨基葡萄糖苷酶选择性抑制剂的合成、评价及机制。
Chembiochem. 2011 Feb 11;12(3):457-67. doi: 10.1002/cbic.201000561. Epub 2010 Dec 23.
7
Action pattern of Streptomyces griseus chitinase on partially N-acetylated chitosan.灰色链霉菌几丁质酶对部分N-乙酰化壳聚糖的作用模式
Agric Biol Chem. 1990 Dec;54(12):3191-9.
8
Insights into the structure-affinity relationships and solvation effects between OfHex1 and inhibitors using molecular dynamics simulations.利用分子动力学模拟深入了解OfHex1与抑制剂之间的结构-亲和力关系及溶剂化效应。
J Mol Graph Model. 2019 Jul;90:1-8. doi: 10.1016/j.jmgm.2019.03.022. Epub 2019 Mar 27.
9
Pochonicine, a polyhydroxylated pyrrolizidine alkaloid from fungus Pochonia suchlasporia var. suchlasporia TAMA 87 as a potent beta-N-acetylglucosaminidase inhibitor.多羟基吡咯里西啶生物碱来自真菌拟茎点霉 TAMA 87 变种 suchlasporia 中的波壳宁碱,是一种有效的β-N-乙酰氨基葡萄糖苷酶抑制剂。
Bioorg Med Chem. 2009 Oct 15;17(20):7248-53. doi: 10.1016/j.bmc.2009.08.052. Epub 2009 Aug 31.
10
A straightforward access to TMG-chitooligomycins and their evaluation as β-N-acetylhexosaminidase inhibitors.一种简便的 TMG-壳寡糖霉素及其作为β-N-乙酰己糖苷酶抑制剂的评价方法。
Carbohydr Res. 2013 Mar 7;368:52-6. doi: 10.1016/j.carres.2012.12.007. Epub 2012 Dec 19.

引用本文的文献

1
Expediting Glycospace Exploration: Therapeutic Glycans via Automated Synthesis.加速糖空间探索:通过自动化合成制备治疗性聚糖
Angew Chem Int Ed Engl. 2025 Mar 24;64(13):e202422766. doi: 10.1002/anie.202422766. Epub 2025 Feb 21.
2
Electrochemically Enabled Total Syntheses of Natural Products.天然产物的电化学全合成
ChemElectroChem. 2023 Jun 1;10(11). doi: 10.1002/celc.202300140. Epub 2023 May 2.
3
Structure-guided computational insecticide discovery targeting -N-acetyl-D-hexosaminidase of .基于结构的靶向-N-乙酰-D-氨基葡萄糖苷酶的计算杀虫剂发现。
J Biomol Struct Dyn. 2024;42(21):11717-11730. doi: 10.1080/07391102.2023.2264394. Epub 2023 Oct 9.
4
Efficient and versatile formation of glycosidic bonds via catalytic strain-release glycosylation with glycosyl ortho-2,2-dimethoxycarbonylcyclopropylbenzoate donors.通过使用糖基邻-2,2-二甲氧基羰基环丙基苯甲酸盐供体的催化应变释放糖基化反应,高效且多功能地形成糖苷键。
Nat Commun. 2023 Jul 7;14(1):4010. doi: 10.1038/s41467-023-39619-7.
5
Endophytic actinobacteria from wild medicinal plants are a natural source of insecticide to control the African cotton leafworm (Spodoptera littoralis).来自野生药用植物的内生放线菌是控制非洲棉叶虫(埃及棉铃虫)的天然杀虫剂来源。
AMB Express. 2023 May 15;13(1):47. doi: 10.1186/s13568-023-01550-x.
6
An orthogonal and reactivity-based one-pot glycosylation strategy for both glycan and nucleoside synthesis: access to TMG-chitotriomycin, lipochitooligosaccharides and capuramycin.一种用于聚糖和核苷合成的基于正交性和反应性的一锅法糖基化策略:合成TMG-壳三霉素、脂壳寡糖和卡普霉素。
Chem Sci. 2021 Feb 23;12(14):5143-5151. doi: 10.1039/d0sc06815b.
7
New analogs of pochonicine, a potent β--acetylglucosaminidase inhibitor from fungus var. TAMA 87.波卓宁(pochonicine)的新型类似物,一种从真菌变种TAMA 87中提取的强效β-乙酰氨基葡萄糖苷酶抑制剂
J Pestic Sci. 2021 Feb 20;46(1):115-119. doi: 10.1584/jpestics.D20-086.
8
Computational Studies on the Potency and Selectivity of PUGNAc Derivatives Against GH3, GH20, and GH84 β-N-acetyl-D-hexosaminidases.PUGNAc衍生物对GH3、GH20和GH84β-N-乙酰-D-己糖胺酶的效力和选择性的计算研究
Front Chem. 2019 Apr 12;7:235. doi: 10.3389/fchem.2019.00235. eCollection 2019.
9
Computational Study for the Unbinding Routes of β--Acetyl-d-Hexosaminidase Inhibitor: Insight from Steered Molecular Dynamics Simulations.β-乙酰-d-己糖苷酶抑制剂解缚途径的计算研究:来自导向分子动力学模拟的洞察。
Int J Mol Sci. 2019 Mar 26;20(6):1516. doi: 10.3390/ijms20061516.
10
Total synthesis of TMG-chitotriomycin based on an automated electrochemical assembly of a disaccharide building block.基于二糖构建模块的自动化电化学组装全合成TMG-壳三霉素。
Beilstein J Org Chem. 2017 May 16;13:919-924. doi: 10.3762/bjoc.13.93. eCollection 2017.