• 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

邻苯恶唑啉A,一种源自微生物的纤维素生物合成特异性抑制剂。I. 发现、产生微生物的分类学、发酵及生物活性。

Phthoxazolin A, a specific inhibitor of cellulose biosynthesis from microbial origin. I. Discovery, taxonomy of producing microorganism, fermentation, and biological activity.

作者信息

Tanaka Y, Kanaya I, Takahashi Y, Shinose M, Tanaka H, Omura S

机构信息

Research Center for Biological Function, Kitasato Institute, School of Pharmaceutical Sciences, Kitasato University, Tokyo, Japan.

出版信息

J Antibiot (Tokyo). 1993 Aug;46(8):1208-13. doi: 10.7164/antibiotics.46.1208.

DOI:10.7164/antibiotics.46.1208
PMID:8407582
Abstract

A new inhibitor of cellulose biosynthesis named phthoxazolin A was discovered as a metabolite of Streptomyces sp. OM-5714. A newly established screening method, which utilized a cellulose-containing fungus, Phytophthora sp. as a test organism, was successfully employed for discovery of the compound. Phthoxazolin A, C16H22N2O3 (MW of 290), is a lipophilic triene compound with an oxazole moiety. It has moderate antifungal activity against Phytophthora spp. only and has potent herbicidal activity. Phosphate-limited fermentation conditions favored production of the active compound.

摘要

一种名为邻苯恶唑啉A的新型纤维素生物合成抑制剂,作为链霉菌属OM-5714的代谢产物被发现。一种新建立的筛选方法,利用含纤维素的真菌疫霉属作为测试生物,成功用于该化合物的发现。邻苯恶唑啉A,C16H22N2O3(分子量290),是一种带有恶唑部分的亲脂性三烯化合物。它仅对疫霉属具有中等抗真菌活性,并具有强效除草活性。磷酸盐限制的发酵条件有利于活性化合物的产生。

相似文献

1
Phthoxazolin A, a specific inhibitor of cellulose biosynthesis from microbial origin. I. Discovery, taxonomy of producing microorganism, fermentation, and biological activity.邻苯恶唑啉A,一种源自微生物的纤维素生物合成特异性抑制剂。I. 发现、产生微生物的分类学、发酵及生物活性。
J Antibiot (Tokyo). 1993 Aug;46(8):1208-13. doi: 10.7164/antibiotics.46.1208.
2
Phthoxazolin A, a specific inhibitor of cellulose biosynthesis from microbial origin. II. Isolation, physico-chemical properties, and structural elucidation.毒锈菌素A,一种源自微生物的纤维素生物合成特异性抑制剂。II. 分离、理化性质及结构解析。
J Antibiot (Tokyo). 1993 Aug;46(8):1214-8. doi: 10.7164/antibiotics.46.1214.
3
Screening method for cellulose biosynthesis inhibitors with herbicidal activity.具有除草活性的纤维素生物合成抑制剂的筛选方法。
J Antibiot (Tokyo). 1995 Jul;48(7):720-4. doi: 10.7164/antibiotics.48.720.
4
Phthoxazolin, a specific inhibitor of cellulose biosynthesis, produced by a strain of Streptomyces sp.稻瘟唑啉,一种由链霉菌属的一个菌株产生的纤维素生物合成的特异性抑制剂。
J Antibiot (Tokyo). 1990 Aug;43(8):1034-6. doi: 10.7164/antibiotics.43.1034.
5
New antibiotics phthoxazolins B, C and D produced by Streptomyces sp. KO-7888.链霉菌属KO-7888产生的新型抗生素恶唑啉B、C和D。
J Antibiot (Tokyo). 1995 Jul;48(7):714-9. doi: 10.7164/antibiotics.48.714.
6
Synthesis and biological activity of derivatives of the herbicidal metabolite CL22T (phthoxazolin).除草代谢物CL22T(邻苯恶唑啉)衍生物的合成及生物活性
J Antibiot (Tokyo). 1995 Apr;48(4):341-3. doi: 10.7164/antibiotics.48.341.
7
Activation of cryptic phthoxazolin A production in Streptomyces avermitilis by the disruption of autoregulator-receptor homologue AvaR3.通过破坏自调节受体同源物AvaR3激活阿维链霉菌中隐蔽的恶唑啉A的产生。
J Biosci Bioeng. 2017 Dec;124(6):611-617. doi: 10.1016/j.jbiosc.2017.06.014. Epub 2017 Jul 17.
8
Herboxidiene, a new herbicidal substance from Streptomyces chromofuscus A7847. Taxonomy, fermentation, isolation, physico-chemical and biological properties.赫泊西定,一种来自暗褐链霉菌A7847的新型除草物质。分类学、发酵、分离、理化性质及生物学特性
J Antibiot (Tokyo). 1992 Jun;45(6):914-21. doi: 10.7164/antibiotics.45.914.
9
Characterization of the biosynthetic gene cluster for cryptic phthoxazolin A in Streptomyces avermitilis.阿维链霉菌中隐性毒杀唑啉A生物合成基因簇的表征
PLoS One. 2018 Jan 11;13(1):e0190973. doi: 10.1371/journal.pone.0190973. eCollection 2018.
10
U-42, 126, a new antimetabolite antibiotic: production, biological activity, and taxonomy of the producing microorganism.U - 42,126,一种新型抗代谢物抗生素:产生菌的生产、生物活性及分类学
Antimicrob Agents Chemother. 1973 Mar;3(3):425-31. doi: 10.1128/AAC.3.3.425.

引用本文的文献

1
comparative genome analysis demonstrates genome heterogeneity and reduction in species isolated from animals and associated with human illness.比较基因组分析表明,从动物分离出并与人类疾病相关的物种存在基因组异质性和基因组缩减。
Heliyon. 2023 Jun 27;9(7):e17652. doi: 10.1016/j.heliyon.2023.e17652. eCollection 2023 Jul.
2
The oxazolomycin family: a review of current knowledge.恶唑霉素家族:当前知识综述
RSC Adv. 2020 Nov 9;10(67):40745-40794. doi: 10.1039/d0ra08396h.
3
Oxazolomycins produced by and their cytotoxic activity.由……产生的恶唑霉素及其细胞毒性活性。 (原句表述不完整,推测是这样翻译,完整准确的句子应该是“由……产生的恶唑霉素及其细胞毒性活性的研究”之类,这里根据现有内容尽量贴近原意翻译)
RSC Adv. 2021 Oct 28;11(55):35011-35019. doi: 10.1039/d1ra06182h. eCollection 2021 Oct 25.
4
Antimicrobial Compounds from Microorganisms.微生物来源的抗菌化合物。
Antibiotics (Basel). 2022 Feb 22;11(3):285. doi: 10.3390/antibiotics11030285.
5
Kinetic resolution of racemic allylic alcohols iridium-catalyzed asymmetric hydrogenation: scope, synthetic applications and insight into the origin of selectivity.外消旋烯丙醇的动力学拆分:铱催化不对称氢化反应的范围、合成应用及选择性起源的深入研究
Chem Sci. 2020 Dec 8;12(5):1937-1943. doi: 10.1039/d0sc05276k.
6
Progress in the total synthesis of inthomycins.硬皮马勃菌素全合成的进展
Beilstein J Org Chem. 2021 Jan 7;17:58-82. doi: 10.3762/bjoc.17.7. eCollection 2021.
7
Short, Tin-Free Synthesis of All Three Inthomycins.短、无锡合成三种茵芋碱。
Chemistry. 2018 Nov 13;24(63):16753-16756. doi: 10.1002/chem.201803794. Epub 2018 Oct 19.
8
Phthoxazolin A inhibits prostate cancer growth by modulating tumor-stromal cell interactions.邻苯恶唑啉A通过调节肿瘤-基质细胞相互作用来抑制前列腺癌生长。
Cancer Sci. 2009 Jan;100(1):150-7. doi: 10.1111/j.1349-7006.2008.00996.x. Epub 2008 Oct 20.
9
Recent examples of novel secondary metabolites.新型次生代谢产物的近期实例。
Folia Microbiol (Praha). 1995;40(1):31-42. doi: 10.1007/BF02816526.