• 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

相似文献

1
Genetic analysis of Bacillus subtilis spo mutations generated by Tn917-mediated insertional mutagenesis.通过Tn917介导的插入诱变产生的枯草芽孢杆菌spo突变的遗传分析。
Genetics. 1987 Dec;117(4):603-17. doi: 10.1093/genetics/117.4.603.
2
Genetic transposition and insertional mutagenesis in Bacillus subtilis with Streptococcus faecalis transposon Tn917.利用粪肠球菌转座子Tn917对枯草芽孢杆菌进行基因转座和插入诱变。
Proc Natl Acad Sci U S A. 1983 Apr;80(8):2305-9. doi: 10.1073/pnas.80.8.2305.
3
srfA is an operon required for surfactin production, competence development, and efficient sporulation in Bacillus subtilis.srfA是枯草芽孢杆菌中产生表面活性素、感受态发育和高效芽孢形成所必需的一个操纵子。
J Bacteriol. 1991 Mar;173(5):1770-8. doi: 10.1128/jb.173.5.1770-1778.1991.
4
Insertional mutagenesis of Listeria monocytogenes with a novel Tn917 derivative that allows direct cloning of DNA flanking transposon insertions.用一种新型Tn917衍生物对单核细胞增生李斯特菌进行插入诱变,该衍生物可直接克隆转座子插入侧翼的DNA。
J Bacteriol. 1990 Jul;172(7):3738-44. doi: 10.1128/jb.172.7.3738-3744.1990.
5
Isolation of Bacillus subtilis transformation-deficient mutants and mapping of competence genes.枯草芽孢杆菌转化缺陷型突变体的分离及感受态基因的定位
Genet Res. 1989 Aug;54(1):1-5. doi: 10.1017/s0016672300028305.
6
A novel method for the rapid cloning in Escherichia coli of Bacillus subtilis chromosomal DNA adjacent to Tn917 insertions.一种在大肠杆菌中快速克隆与Tn917插入位点相邻的枯草芽孢杆菌染色体DNA的新方法。
Mol Gen Genet. 1984;195(3):424-33. doi: 10.1007/BF00341443.
7
Effects of transition mutations in the regulatory locus spoIIA on the incidence of sporulation in Bacillus subtilis.
J Gen Microbiol. 1985 Apr;131(4):959-62. doi: 10.1099/00221287-131-4-959.
8
Genetic and phenotypic characterization of a cluster of mutations in the spoVA locus of Bacillus subtilis.枯草芽孢杆菌spoVA基因座中一组突变的遗传和表型特征分析
J Gen Microbiol. 1984 Aug;130(8):2115-21. doi: 10.1099/00221287-130-8-2115.
9
Construction and properties of Tn917-lac, a transposon derivative that mediates transcriptional gene fusions in Bacillus subtilis.Tn917-lac的构建及其特性,一种介导枯草芽孢杆菌转录基因融合的转座子衍生物。
Proc Natl Acad Sci U S A. 1986 Jan;83(1):140-4. doi: 10.1073/pnas.83.1.140.
10
Characterization of the Bacillus subtilis sporulation gene spoVK.枯草芽孢杆菌芽孢形成基因spoVK的特性分析
J Bacteriol. 1992 Feb;174(3):1053-4. doi: 10.1128/jb.174.3.1053-1054.1992.

引用本文的文献

1
Phosphorelay changes and plasticity underlie the life history evolution of sporulation and germination in serial batch culture.磷酸化信号转导变化和可塑性是连续分批培养中孢子形成和萌发的生活史进化的基础。
Microbiology (Reading). 2025 Mar;171(3). doi: 10.1099/mic.0.001540.
2
Large Roles of Small Proteins.小分子的大作用。
Annu Rev Microbiol. 2024 Nov;78(1):1-22. doi: 10.1146/annurev-micro-112723-083001. Epub 2024 Nov 7.
3
Catabolism of germinant amino acids is required to prevent premature spore germination in .芽殖氨基酸的分解代谢对于防止 在过早的孢子萌发是必需的。
mBio. 2024 May 8;15(5):e0056224. doi: 10.1128/mbio.00562-24. Epub 2024 Apr 2.
4
Fatty Acid Synthesis Knockdown Promotes Biofilm Wrinkling and Inhibits Sporulation in Bacillus subtilis.脂肪酸合成敲低促进枯草芽孢杆菌生物膜起皱并抑制孢子形成。
mBio. 2022 Oct 26;13(5):e0138822. doi: 10.1128/mbio.01388-22. Epub 2022 Sep 7.
5
Asymmetric localization of the cell division machinery during sporulation.细胞分裂机制在孢子形成过程中的不对称定位。
Elife. 2021 May 21;10:e62204. doi: 10.7554/eLife.62204.
6
Milestones in sporulation research.孢子形成研究中的里程碑。
Microb Cell. 2020 Nov 27;8(1):1-16. doi: 10.15698/mic2021.01.739.
7
Chromosome Translocation Inflates Bacillus Forespores and Impacts Cellular Morphology.染色体易位使芽孢杆菌膨胀并影响细胞形态。
Cell. 2018 Feb 8;172(4):758-770.e14. doi: 10.1016/j.cell.2018.01.027.
8
Phenotypic memory in Bacillus subtilis links dormancy entry and exit by a spore quantity-quality tradeoff.枯草芽孢杆菌中的表型记忆通过孢子数量-质量权衡将休眠的进入和退出联系起来。
Nat Commun. 2018 Jan 4;9(1):69. doi: 10.1038/s41467-017-02477-1.
9
Genetic networks controlled by the bacterial replication initiator and transcription factor DnaA in Bacillus subtilis.枯草芽孢杆菌中由细菌复制起始蛋白和转录因子DnaA控制的遗传网络。
Mol Microbiol. 2017 Oct;106(1):109-128. doi: 10.1111/mmi.13755. Epub 2017 Aug 11.
10
A Novel Cell Type Enables to Escape from Unsuccessful Sporulation in Minimal Medium.一种新型细胞类型能够在基本培养基中从不成功的孢子形成中逃脱。
Front Microbiol. 2016 Nov 11;7:1810. doi: 10.3389/fmicb.2016.01810. eCollection 2016.

本文引用的文献

1
New ways to study developmental genes in spore-forming bacteria.研究孢子形成菌发育基因的新方法。
Science. 1985 Apr 19;228(4697):285-91. doi: 10.1126/science.228.4697.285.
2
Colorimetric assay for dipicolinic acid in bacterial spores.细菌芽孢中吡啶二羧酸的比色测定法。
Science. 1958 Jan 3;127(3288):26-7. doi: 10.1126/science.127.3288.26.
3
Identification of a new developmental locus in Bacillus subtilis by construction of a deletion mutation in a cloned gene under sporulation control.通过构建受芽孢形成控制的克隆基因中的缺失突变来鉴定枯草芽孢杆菌中的一个新发育位点。
J Bacteriol. 1981 Oct;148(1):341-51. doi: 10.1128/jb.148.1.341-351.1981.
4
The Bacillus subtilis chromosome.枯草芽孢杆菌染色体。
Microbiol Rev. 1980 Mar;44(1):57-82. doi: 10.1128/mr.44.1.57-82.1980.
5
Identification of a sporulation locus in cloned Bacillus subtilis deoxyribonucleic acid.克隆的枯草芽孢杆菌脱氧核糖核酸中一个芽孢形成位点的鉴定。
J Bacteriol. 1980 Apr;142(1):331-4. doi: 10.1128/jb.142.1.331-334.1980.
6
Use of a lacZ fusion to study the role of the spoO genes of Bacillus subtilis in developmental regulation.利用lacZ融合技术研究枯草芽孢杆菌spoO基因在发育调控中的作用。
Cell. 1983 Nov;35(1):275-83. doi: 10.1016/0092-8674(83)90230-1.
7
SpoVH and spoVJ--new sporulation loci in Bacillus subtilis 168.SpoVH和spoVJ——枯草芽孢杆菌168中的新孢子形成基因座。
J Gen Microbiol. 1983 Feb;129(2):293-302. doi: 10.1099/00221287-129-2-293.
8
Genetic transposition and insertional mutagenesis in Bacillus subtilis with Streptococcus faecalis transposon Tn917.利用粪肠球菌转座子Tn917对枯草芽孢杆菌进行基因转座和插入诱变。
Proc Natl Acad Sci U S A. 1983 Apr;80(8):2305-9. doi: 10.1073/pnas.80.8.2305.
9
Construction of a cloning site near one end of Tn917 into which foreign DNA may be inserted without affecting transposition in Bacillus subtilis or expression of the transposon-borne erm gene.在Tn917一端附近构建一个克隆位点,可在其中插入外源DNA,而不影响其在枯草芽孢杆菌中的转座或转座子携带的erm基因的表达。
Plasmid. 1984 Jul;12(1):1-9. doi: 10.1016/0147-619x(84)90061-1.
10
A novel method for the rapid cloning in Escherichia coli of Bacillus subtilis chromosomal DNA adjacent to Tn917 insertions.一种在大肠杆菌中快速克隆与Tn917插入位点相邻的枯草芽孢杆菌染色体DNA的新方法。
Mol Gen Genet. 1984;195(3):424-33. doi: 10.1007/BF00341443.

通过Tn917介导的插入诱变产生的枯草芽孢杆菌spo突变的遗传分析。

Genetic analysis of Bacillus subtilis spo mutations generated by Tn917-mediated insertional mutagenesis.

作者信息

Sandman K, Losick R, Youngman P

机构信息

Department of Cellular and Developmental Biology, Harvard University, Cambridge, Massachusetts 02138.

出版信息

Genetics. 1987 Dec;117(4):603-17. doi: 10.1093/genetics/117.4.603.

DOI:10.1093/genetics/117.4.603
PMID:2828153
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1203235/
Abstract

Mutations that cause sporulation defects (spo mutations) often identify developmentally regulated transcription units or genes whose products are required for the expression of sporulation-specific regulons. We report here the isolation, genetic analysis and phenotypic characterization of spo mutations produced by insertional mutagenesis with transposon Tn917, a form of mutagenesis that facilitates genetic and physical manipulation of mutated genes in many ways. Twenty-four insertional spo mutations were studied in detail. On the basis of transformation-mediated and transduction-mediated linkage analysis and a range of phenotypic tests, these mutations were assigned to 20 distinct loci, at least 9 of which are different from the 40 previously described spo loci. The insertional mutations caused blocks at a variety of different stages of sporulation, and therefore probably identify genes active at different times during sporulation. In addition to increasing substantially the total of known spo loci, we anticipate that this collection will include representatives of many of the temporally regulated sets of genes that comprise the overall program of sporulation-specific gene activation in Bacillus subtilis. Given the kinds of manipulations that are possible with genes disrupted by Tn917 insertions, this should significantly facilitate efforts to understand the regulation of these gene sets.

摘要

导致芽孢形成缺陷的突变(spo突变)常常能鉴定出发育调控的转录单元或基因,其产物是芽孢形成特异性调控子表达所必需的。我们在此报告通过转座子Tn917进行插入诱变产生的spo突变的分离、遗传分析及表型特征,这种诱变形式在许多方面有助于对突变基因进行遗传和物理操作。我们详细研究了24个插入性spo突变。基于转化介导和转导介导的连锁分析以及一系列表型测试,这些突变被定位到20个不同的位点,其中至少9个与先前描述的40个spo位点不同。插入突变在芽孢形成的各种不同阶段造成阻断,因此可能鉴定出在芽孢形成过程中不同时间活跃的基因。除了大幅增加已知spo位点的总数外,我们预计这个集合将包括许多时间调控基因集的代表,这些基因集构成了枯草芽孢杆菌芽孢形成特异性基因激活的总体程序。鉴于通过Tn917插入破坏的基因可以进行各种操作,这应该会显著促进对这些基因集调控的理解。