• 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

刺孢霉素的研究。I. 刺孢霉素A的分离与特性

Studies on aculeacin. I. Isolation and characterization of aculeacin A.

作者信息

Mizuno K, Yagi A, Satoi S, Takada M, Hayashi M

出版信息

J Antibiot (Tokyo). 1977 Apr;30(4):297-302. doi: 10.7164/antibiotics.30.297.

DOI:10.7164/antibiotics.30.297
PMID:324959
Abstract

Aculeacin A, a new antifungal antibiotic was isolated from the mycelial cake of Aspergillus aculeatus M-4214. The antibiotic is a white amorphous powder soluble in lower alcohols and hardly soluble in other organic solvents or water. Aculeacin A gave palmitic acid and five ninhydrin-positive products including theonine, hydroxyproline upon acid hydrolysis. The antibiotic showed a potent activity against molds and yeasts, but exhibited no antibacterial activity. Aculeacin A has relatively low toxicity in mice.

摘要

刺孢曲菌素A是从棘孢曲霉M-4214的菌丝饼中分离出的一种新型抗真菌抗生素。该抗生素为白色无定形粉末,可溶于低级醇类,几乎不溶于其他有机溶剂或水。刺孢曲菌素A经酸水解后产生棕榈酸和5种茚三酮阳性产物,包括苏氨酸、羟脯氨酸。该抗生素对霉菌和酵母菌显示出强效活性,但无抗菌活性。刺孢曲菌素A对小鼠的毒性相对较低。

相似文献

1
Studies on aculeacin. I. Isolation and characterization of aculeacin A.刺孢霉素的研究。I. 刺孢霉素A的分离与特性
J Antibiot (Tokyo). 1977 Apr;30(4):297-302. doi: 10.7164/antibiotics.30.297.
2
Studies on aculeacin. II. Isolation and characterization of aculeacins B, C, D, E, F and G.刺孢霉素的研究。II. 刺孢霉素B、C、D、E、F和G的分离与特性
J Antibiot (Tokyo). 1977 Apr;30(4):303-7. doi: 10.7164/antibiotics.30.303.
3
Papulacandins, a new family of antibiotics with antifungal activity, I. Fermentation, isolation, chemical and biological characterization of papulacandins A, B, C, D and E.丘疹霉素,一类具有抗真菌活性的新型抗生素,I. 丘疹霉素A、B、C、D和E的发酵、分离、化学及生物学特性
J Antibiot (Tokyo). 1977 Apr;30(4):289-96. doi: 10.7164/antibiotics.30.289.
4
L-671,329, a new antifungal agent. III. In vitro activity, toxicity and efficacy in comparison to aculeacin.新型抗真菌剂L-671,329。III. 与棘霉素相比的体外活性、毒性及疗效
J Antibiot (Tokyo). 1989 Feb;42(2):174-8. doi: 10.7164/antibiotics.42.174.
5
[Effects of aculeacin A on Candida albicans and the transformation of lymphocytes in vitro].阿库拉霉素A对白色念珠菌及体外淋巴细胞转化的影响
Josai Shika Daigaku Kiyo. 1982;11(3):323-42.
6
Mulundocandin, a new lipopeptide antibiotic. I. Taxonomy, fermentation, isolation and characterization.穆伦多卡菌素,一种新型脂肽抗生素。I. 分类学、发酵、分离与特性
J Antibiot (Tokyo). 1987 Mar;40(3):275-80. doi: 10.7164/antibiotics.40.275.
7
In vitro studies of aculeacin A, a new antifungal antibiotic.新抗真菌抗生素阿库拉辛A的体外研究
J Antibiot (Tokyo). 1982 Feb;35(2):203-9. doi: 10.7164/antibiotics.35.203.
8
Rapamycin (AY-22,989), a new antifungal antibiotic. I. Taxonomy of the producing streptomycete and isolation of the active principle.雷帕霉素(AY - 22,989),一种新型抗真菌抗生素。I. 产生该抗生素的链霉菌的分类及活性成分的分离
J Antibiot (Tokyo). 1975 Oct;28(10):721-6. doi: 10.7164/antibiotics.28.721.
9
Cispentacin, a new antifungal antibiotic. I. Production, isolation, physico-chemical properties and structure.
J Antibiot (Tokyo). 1989 Dec;42(12):1749-55. doi: 10.7164/antibiotics.42.1749.
10
Isolation of CB-25-I, an antifungal antibiotic, from Serratia plymuthica.从粘质沙雷氏菌中分离抗真菌抗生素CB-25-I。
J Antibiot (Tokyo). 1989 Jun;42(6):869-74. doi: 10.7164/antibiotics.42.869.

引用本文的文献

1
Innovations in Antifungal Drug Discovery among Cell Envelope Synthesis Enzymes through Structural Insights.通过结构洞察实现细胞包膜合成酶抗真菌药物发现的创新。
J Fungi (Basel). 2024 Feb 22;10(3):171. doi: 10.3390/jof10030171.
2
Natural Products That Contain Higher Homologated Amino Acids.含有高级同系氨基酸的天然产物。
Chembiochem. 2024 May 2;25(9):e202300822. doi: 10.1002/cbic.202300822. Epub 2024 Apr 9.
3
Cyclic Peptides with Antifungal Properties Derived from Bacteria, Fungi, Plants, and Synthetic Sources.源自细菌、真菌、植物及合成来源的具有抗真菌特性的环肽
Pharmaceuticals (Basel). 2023 Jun 18;16(6):892. doi: 10.3390/ph16060892.
4
Substituted l-tryptophan-l-phenyllactic acid conjugates produced by an endophytic fungus using an OSMAC approach.一株内生真菌采用OSMAC方法产生的取代L-色氨酸-L-苯乳酸共轭物。
RSC Adv. 2018 Feb 19;8(14):7863-7872. doi: 10.1039/c8ra00200b. eCollection 2018 Feb 14.
5
Echinocandins: structural diversity, biosynthesis, and development of antimycotics.棘白菌素类药物:结构多样性、生物合成和抗真菌药物的开发。
Appl Microbiol Biotechnol. 2021 Jan;105(1):55-66. doi: 10.1007/s00253-020-11022-y. Epub 2020 Dec 3.
6
Antimicrobial Peptides: a New Frontier in Antifungal Therapy.抗菌肽:抗真菌治疗的新前沿。
mBio. 2020 Nov 3;11(6):e02123-20. doi: 10.1128/mBio.02123-20.
7
Comparative Transcriptomics Analysis of the Responses of the Filamentous Fungus to Different Carbon Sources.丝状真菌对不同碳源响应的比较转录组学分析
Front Microbiol. 2020 Feb 18;11:190. doi: 10.3389/fmicb.2020.00190. eCollection 2020.
8
Functional redundancy in Echinocandin B in-cluster transcription factor B of NRRL 11440.棘白菌素B在NRRL 11440的簇内转录因子B中的功能冗余。
Biotechnol Rep (Amst). 2018 Jun 9;19:e00264. doi: 10.1016/j.btre.2018.e00264. eCollection 2018 Sep.
9
Structural Diversity and Biological Activities of Fungal Cyclic Peptides, Excluding Cyclodipeptides.真菌环肽的结构多样性和生物活性,不包括环二肽。
Molecules. 2017 Nov 27;22(12):2069. doi: 10.3390/molecules22122069.
10
Evolution of Chemical Diversity in Echinocandin Lipopeptide Antifungal Metabolites.棘白菌素脂肽类抗真菌代谢产物中化学多样性的演变
Eukaryot Cell. 2015 Jul;14(7):698-718. doi: 10.1128/EC.00076-15. Epub 2015 May 29.