• 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

通过诺加链霉菌诺拉霉素生物合成基因的异源表达生产杂合蒽环类抗生素。

Production of hybrid anthracycline antibiotics by heterologous expression of Streptomyces nogalater nogalamycin biosynthesis genes.

作者信息

Ylihonko K, Hakala J, Kunnari T, Mäntsälä P

机构信息

Department of Biochemistry and Food Chemistry, University of Turku, Finland.

出版信息

Microbiology (Reading). 1996 Aug;142 ( Pt 8):1965-72. doi: 10.1099/13500872-142-8-1965.

DOI:10.1099/13500872-142-8-1965
PMID:8760909
Abstract

A cluster of anthracycline biosynthetic genes isolated from Streptomyces nogalater was expressed in Streptomyces lividans and in Streptomyces galilaeus. A 12 kb DNA fragment cloned from this cluster in pIJ486 caused the production of a novel compound when introduced into S. lividans. The compound is derived from nogalonic acid methyl ester, an early intermediate in nogalamycin biosynthesis. Complementation with the cloned 12 kb fragment of S. galilaeus mutants blocked in aclacinomycin biosynthesis caused the production of hybrid anthracyclines. Cloning of the nogalamycin gene cluster should make possible a detailed study of the biosynthesis of this interesting antibiotic, as well as the production of novel anthracyclines of potential value as cytostatic drugs.

摘要

从诺加链霉菌中分离出的一组蒽环类生物合成基因在淡紫链霉菌和加利利链霉菌中表达。从该基因簇中克隆到pIJ486中的一个12 kb DNA片段导入淡紫链霉菌后可产生一种新化合物。该化合物衍生自诺加霉素生物合成早期中间体诺加洛酸甲酯。用在阿克拉霉素生物合成中受阻的加利利链霉菌突变体的克隆12 kb片段进行互补,可产生杂合蒽环类化合物。克隆诺加霉素基因簇将有可能详细研究这种有趣抗生素的生物合成,以及生产具有潜在细胞抑制药物价值的新型蒽环类化合物。

相似文献

1
Production of hybrid anthracycline antibiotics by heterologous expression of Streptomyces nogalater nogalamycin biosynthesis genes.通过诺加链霉菌诺拉霉素生物合成基因的异源表达生产杂合蒽环类抗生素。
Microbiology (Reading). 1996 Aug;142 ( Pt 8):1965-72. doi: 10.1099/13500872-142-8-1965.
2
The entire nogalamycin biosynthetic gene cluster of Streptomyces nogalater: characterization of a 20-kb DNA region and generation of hybrid structures.
Mol Genet Genomics. 2001 Oct;266(2):276-88. doi: 10.1007/s004380100554.
3
A gene cluster involved in nogalamycin biosynthesis from Streptomyces nogalater: sequence analysis and complementation of early-block mutations in the anthracycline pathway.来自诺加链霉菌的参与诺加霉素生物合成的基因簇:蒽环类途径中早期阻断突变的序列分析与互补作用
Mol Gen Genet. 1996 May 23;251(2):113-20. doi: 10.1007/BF02172908.
4
Elucidation of anthracyclinone biosynthesis by stepwise cloning of genes for anthracyclines from three different Streptomyces spp.通过逐步克隆来自三种不同链霉菌属物种的蒽环类药物基因来阐明蒽环酮生物合成
Microbiology (Reading). 2000 Jan;146 ( Pt 1):155-163. doi: 10.1099/00221287-146-1-155.
5
Identification of a cyclase gene dictating the C-9 stereochemistry of anthracyclines from Streptomyces nogalater.鉴定决定诺加链霉菌蒽环类抗生素C-9立体化学的环化酶基因。
Antimicrob Agents Chemother. 2000 Feb;44(2):396-9. doi: 10.1128/AAC.44.2.396-399.2000.
6
Hybrid anthracyclines from a genetically engineered Streptomyces galilaeus mutant.
J Org Chem. 2000 May 19;65(10):2851-5. doi: 10.1021/jo980345o.
7
Isolation and characterization of 8-demethoxy steffimycins and generation of 2,8-demethoxy steffimycins in Streptomyces steffisburgensis by the nogalamycin biosynthesis genes.通过诺加霉素生物合成基因从施氏链霉菌中分离和鉴定8-去甲氧基斯特菲霉素以及生成2,8-去甲氧基斯特菲霉素
J Antibiot (Tokyo). 1997 Jun;50(6):496-501. doi: 10.7164/antibiotics.50.496.
8
[Role of the snorA gene in nogalamycin biosynthesis by strain Streptomyces nogalater Lv65 ].
Mikrobiologiia. 2011 Jul-Aug;80(4):490-5.
9
Characterization of Streptomyces nogalater genes encoding enzymes involved in glycosylation steps in nogalamycin biosynthesis.
Mol Gen Genet. 1997 Sep;256(2):203-9. doi: 10.1007/s004380050562.
10
[THE ROLE OF STREPTOMYCES NOGALATER Lv65 snoaM, snoaL and snoaE GENES IN NOGALAMYCIN BIOSYNTHESIS].
Tsitol Genet. 2015 May-Jun;49(3):9-16.

引用本文的文献

1
Discovery of Noncanonical Iron and 2-Oxoglutarate Dependent Enzymes Involved in C-C and C-N Bond Formation in Biosynthetic Pathways.发现参与生物合成途径中碳-碳和碳-氮键形成的非经典铁和2-氧代戊二酸依赖性酶。
ACS Bio Med Chem Au. 2025 Mar 10;5(2):238-261. doi: 10.1021/acsbiomedchemau.5c00001. eCollection 2025 Apr 16.
2
A BioBricks Metabolic Engineering Platform for the Biosynthesis of Anthracyclinones in .在... 中生物砖代谢工程平台用于蒽环类抗生素的生物合成。
ACS Synth Biol. 2022 Dec 16;11(12):4193-4209. doi: 10.1021/acssynbio.2c00498. Epub 2022 Nov 15.
3
Heterologous expression of pikromycin biosynthetic gene cluster using Streptomyces artificial chromosome system.
利用链霉菌人工染色体系统进行匹克霉素生物合成基因簇的异源表达。
Microb Cell Fact. 2017 May 31;16(1):96. doi: 10.1186/s12934-017-0708-7.
4
Cloning and Heterologous Expression of a Large-sized Natural Product Biosynthetic Gene Cluster in Species.一个大型天然产物生物合成基因簇在物种中的克隆与异源表达。
Front Microbiol. 2017 Mar 15;8:394. doi: 10.3389/fmicb.2017.00394. eCollection 2017.
5
Natural products for cancer chemotherapy.用于癌症化疗的天然产物。
Microb Biotechnol. 2011 Nov;4(6):687-99. doi: 10.1111/j.1751-7915.2010.00221.x. Epub 2010 Nov 18.
6
Methods and options for the heterologous production of complex natural products.复杂天然产物的异源生物合成方法和选择。
Nat Prod Rep. 2011 Jan;28(1):125-51. doi: 10.1039/c0np00037j. Epub 2010 Nov 9.
7
Expression, purification and crystallization of the cofactor-independent monooxygenase SnoaB from the nogalamycin biosynthetic pathway.来自诺加霉素生物合成途径的无辅因子单加氧酶SnoaB的表达、纯化及结晶
Acta Crystallogr Sect F Struct Biol Cryst Commun. 2009 Mar 1;65(Pt 3):256-9. doi: 10.1107/S1744309109001389. Epub 2009 Feb 14.
8
Structure of the polyketide cyclase SnoaL reveals a novel mechanism for enzymatic aldol condensation.聚酮环化酶SnoaL的结构揭示了酶促羟醛缩合的新机制。
EMBO J. 2004 May 5;23(9):1911-21. doi: 10.1038/sj.emboj.7600201. Epub 2004 Apr 8.
9
Identification of a cyclase gene dictating the C-9 stereochemistry of anthracyclines from Streptomyces nogalater.鉴定决定诺加链霉菌蒽环类抗生素C-9立体化学的环化酶基因。
Antimicrob Agents Chemother. 2000 Feb;44(2):396-9. doi: 10.1128/AAC.44.2.396-399.2000.