• 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

提高嗜网链霉菌SD-07及其他菌株中接合频率的关键因素。

Crucial factor for increasing the conjugation frequency in Streptomyces netropsis SD-07 and other strains.

作者信息

Wang Xian-Kun, Jin Jian-Ling

机构信息

State Key Laboratory of Microbial Technology, School of Life Sciences, Shandong University, Jinan, China.

出版信息

FEMS Microbiol Lett. 2014 Aug;357(1):99-103. doi: 10.1111/1574-6968.12507. Epub 2014 Jul 7.

DOI:10.1111/1574-6968.12507
PMID:24935520
Abstract

Streptomyces netropsis SD-07, the producer of novel polyene macrolide antifungal antibiotics, was isolated from soil. For the investigation of the functions of its biosynthesis genes and regulation mechanisms, a genetic operating system is necessary. In this study, we successfully transferred the plasmid DNA of pSET152 from the methylation deficient donor, Escherichia coli ET12567/pSET152/pUZ8002, to S. netropsis SD-07 by conjugation and evaluated the crucial factors influencing the conjugation frequency. Ca(2+) ions in presence the conjugation media may increase the conjugation frequency by 1000-10 000 times than Ca(2+) ions absence in the same conjugation media, and 10-100 time higher than Mg(2+) ions. Similar results (increasing the conjugation frequency by 10-100 times when media containing 60 mM CaCl2 ) were also obtained from the conjugation between E. coli ET12567 and Streptomyces coelicolor, S. lavendulae, S. venezuelae, despite their conjugation media were different (MS, CM, GS). So, CaCl2 concentration is a crucial factor for increasing the conjugation frequency, and the suitable concentration may probably be 60 mM. In addition, synthetic medium containing a small amount of organic nitrogen source may benefit increasing the conjugation frequency. These findings could be valuable for the development of a practical method for achieving conjugation in other Streptomyces spp.

摘要

新型多烯大环内酯类抗真菌抗生素的产生菌——暗褐链霉菌SD-07,是从土壤中分离得到的。为了研究其生物合成基因的功能和调控机制,需要一个遗传操作系统。在本研究中,我们通过接合作用成功地将来自甲基化缺陷供体大肠杆菌ET12567/pSET152/pUZ8002的质粒DNA pSET152转移至暗褐链霉菌SD-07,并评估了影响接合频率的关键因素。接合培养基中存在的Ca(2+)离子可使接合频率比相同接合培养基中不存在Ca(2+)离子时提高1000 - 10000倍,且比Mg(2+)离子高10 - 100倍。尽管大肠杆菌ET12567与天蓝色链霉菌、薰衣草链霉菌、委内瑞拉链霉菌之间的接合培养基不同(分别为MS、CM、GS),但当培养基中含有60 mM CaCl2时,也得到了类似的结果(接合频率提高10 - 100倍)。因此,CaCl2浓度是提高接合频率的关键因素,合适的浓度可能为60 mM。此外,含有少量有机氮源的合成培养基可能有利于提高接合频率。这些发现对于开发一种在其他链霉菌属中实现接合的实用方法可能具有重要价值。

相似文献

1
Crucial factor for increasing the conjugation frequency in Streptomyces netropsis SD-07 and other strains.提高嗜网链霉菌SD-07及其他菌株中接合频率的关键因素。
FEMS Microbiol Lett. 2014 Aug;357(1):99-103. doi: 10.1111/1574-6968.12507. Epub 2014 Jul 7.
2
[Construction of conjugal transfer system of Streptomyces venezuelae var. Qinlingensis and the expression of vitreoscilla hemoglobin].[秦岭委内瑞拉链霉菌接合转移系统的构建及透明颤菌血红蛋白的表达]
Wei Sheng Wu Xue Bao. 2010 Mar;50(3):406-10.
3
[Construction of DNA transfer system of Streptomyces tenebrarius].[黑暗链霉菌DNA转移系统的构建]
Wei Sheng Wu Xue Bao. 2002 Apr;42(2):181-5.
4
An efficient gene transfer system for the pimaricin producer Streptomyces natalensis.一种用于制匹马霉素的纳塔尔链霉菌的高效基因转移系统。
FEMS Microbiol Lett. 2006 Apr;257(2):312-8. doi: 10.1111/j.1574-6968.2006.00189.x.
5
[Genetic manipulation system and genomic library of Streptomyces luteosporeus NRRL 2401].[黄色孢子链霉菌NRRL 2401的基因操作系统和基因组文库]
Wei Sheng Wu Xue Bao. 2016 Feb 4;56(2):209-18.
6
Development of an intergeneric conjugal transfer system for xinaomycins-producing Streptomyces noursei Xinao-4.用于生产新娜霉素的诺尔斯链霉菌新娜奥-4的属间接合转移系统的开发。
Int J Mol Sci. 2014 Jul 9;15(7):12217-30. doi: 10.3390/ijms150712217.
7
[Interspecies conjugation of Escherichia coli-Streptomyces globisporus 1912 using integrative plasmid pSET152 and its derivatives].[利用整合质粒pSET152及其衍生物进行大肠杆菌与球形孢链霉菌1912的种间接合]
Genetika. 2001 Oct;37(10):1340-7.
8
[Construction of Escherichia coli-Streptomyces shuttle expression plasmid pMF].[大肠杆菌-链霉菌穿梭表达质粒pMF的构建]
Wei Sheng Wu Xue Bao. 2010 Sep;50(9):1251-7.
9
Intergeneric conjugation in holomycin-producing marine Streptomyces sp. strain M095.产全霉素的海洋链霉菌属菌株M095中的属间接合作用。
Microbiol Res. 2008;163(1):96-104. doi: 10.1016/j.micres.2006.07.003. Epub 2006 Aug 4.
10
Development of a multifunctional and efficient conjugal plasmid for use in Streptomyces spp.用于链霉菌属的多功能高效接合质粒的开发
Appl Microbiol Biotechnol. 2006 May;70(6):705-10. doi: 10.1007/s00253-006-0324-7. Epub 2006 Mar 11.

引用本文的文献

1
Unravelling key enzymatic steps in C-ring cleavage during angucycline biosynthesis.解析安古霉素生物合成过程中C环裂解的关键酶促步骤。
Commun Chem. 2023 Dec 18;6(1):281. doi: 10.1038/s42004-023-01059-1.
2
Redirection of acyl donor metabolic flux for lipopeptide A40926B0 biosynthesis.酰基供体代谢流的重定向用于脂肽 A40926B0 的生物合成。
Microb Biotechnol. 2022 Jun;15(6):1852-1866. doi: 10.1111/1751-7915.14021. Epub 2022 Feb 25.
3
: Recent Insights and Advances.最新见解与进展
J Dent Res. 2021 Jul;100(8):790-797. doi: 10.1177/00220345211000656. Epub 2021 Mar 14.
4
Delivering "Chromatic Bacteria" Fluorescent Protein Tags to Proteobacteria Using Conjugation.通过接合作用将“彩色细菌”荧光蛋白标签递送至变形菌门细菌
Bio Protoc. 2019 Apr 5;9(7):e3199. doi: 10.21769/BioProtoc.3199.
5
Biosynthesis Gene Cluster and Oxazole Ring Formation Enzyme for Inthomycins in sp. Strain SYP-A7193.在 sp. 菌株 SYP-A7193 中合成茵芋素的生物合成基因簇和恶唑环形成酶。
Appl Environ Microbiol. 2020 Oct 1;86(20). doi: 10.1128/AEM.01388-20.
6
Development and optimization of an intergeneric conjugation system and analysis of promoter activity in Streptomyces rimosus M527.开发和优化链霉菌属间杂交系统及分析棘孢小单孢菌 M527 启动子活性。
J Zhejiang Univ Sci B. 2019;20(11):891-900. doi: 10.1631/jzus.B1900270.
7
The Draft Genome Sequence of Actinokineospora bangkokensis 44EHW Reveals the Biosynthetic Pathway of the Antifungal Thailandin Compounds with Unusual Butylmalonyl-CoA Extender Units.曼谷放线嗜皮菌44EHW的基因组序列草图揭示了具有不寻常丁基丙二酰辅酶A延伸单元的抗真菌化合物泰国菌素的生物合成途径。
Molecules. 2016 Nov 23;21(11):1607. doi: 10.3390/molecules21111607.
8
An Efficient Method To Generate Gene Deletion Mutants of the Rapamycin-Producing Bacterium Streptomyces iranensis HM 35.一种高效生成产雷帕霉素细菌伊朗链霉菌HM 35基因缺失突变体的方法。
Appl Environ Microbiol. 2016 May 31;82(12):3481-3492. doi: 10.1128/AEM.00371-16. Print 2016 Jun 15.