• 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

天蓝色链霉菌染色体中dnaA-gyrA区域的基因组织。

Gene organization in the dnaA-gyrA region of the Streptomyces coelicolor chromosome.

作者信息

Calcutt M J

机构信息

Department of Biochemistry, University of Missouri-Columbia 65212.

出版信息

Gene. 1994 Dec 30;151(1-2):23-8. doi: 10.1016/0378-1119(94)90628-9.

DOI:10.1016/0378-1119(94)90628-9
PMID:7828880
Abstract

The gene organization has been determined for an 8-kb portion of the Streptomyces coelicolor chromosome close to the origin of DNA replication (oriC). Hybridization and DNA sequence analyses revealed the presence of five open reading frames (ORFs) oriented in the same direction as the proximal dnaA and dnaN genes. The deduced products of three of the ORFs have been identified as the S. coelicolor homologs of RecF, GyrB and GyrA. These genes are usually clustered in the dnaA region of bacterial chromosomes. In S. coelicolor however, the usual gene arrangement is altered. The recF gene is flanked by two ORFs, one of which encodes a protein with significant similarity to 6-phosphogluconate dehydrogenases (6PGDH), an enzyme that is not immediately linked to DNA metabolism.

摘要

已确定了天蓝色链霉菌染色体中靠近DNA复制起点(oriC)的一个8 kb区域的基因组织。杂交和DNA序列分析表明,存在5个与近端dnaA和dnaN基因方向相同的开放阅读框(ORF)。其中3个ORF的推导产物已被鉴定为RecF、GyrB和GyrA的天蓝色链霉菌同源物。这些基因通常聚集在细菌染色体的dnaA区域。然而,在天蓝色链霉菌中,通常的基因排列发生了改变。recF基因两侧是两个ORF,其中一个编码与6-磷酸葡萄糖酸脱氢酶(6PGDH)具有显著相似性的蛋白质,该酶与DNA代谢并无直接关联。

相似文献

1
Gene organization in the dnaA-gyrA region of the Streptomyces coelicolor chromosome.天蓝色链霉菌染色体中dnaA-gyrA区域的基因组织。
Gene. 1994 Dec 30;151(1-2):23-8. doi: 10.1016/0378-1119(94)90628-9.
2
Cloning and sequencing of the replication origin (oriC) of the Spiroplasma citri chromosome and construction of autonomously replicating artificial plasmids.柑橘螺原体染色体复制起点(oriC)的克隆与测序及自主复制人工质粒的构建。
Curr Microbiol. 1994 Jul;29(1):23-9. doi: 10.1007/BF01570187.
3
An unusual gene containing a dnaJ N-terminal box flanks the putative origin of replication of Mycoplasma genitalium.一个含有dnaJ N端框的不寻常基因位于生殖支原体假定的复制起点两侧。
J Bacteriol. 1994 Sep;176(18):5814-9. doi: 10.1128/jb.176.18.5814-5819.1994.
4
Gene arrangement and organization in a approximately 76 kb fragment encompassing the oriC region of the chromosome of Mycobacterium leprae.包含麻风分枝杆菌染色体oriC区域的约76 kb片段中的基因排列与组织。
Microbiology (Reading). 1996 Nov;142 ( Pt 11):3147-61. doi: 10.1099/13500872-142-11-3147.
5
Conserved gene arrangement in the origin region of the Streptomyces coelicolor chromosome.天蓝色链霉菌染色体起源区域的保守基因排列
J Bacteriol. 1992 May;174(10):3220-6. doi: 10.1128/jb.174.10.3220-3226.1992.
6
Nucleotide sequence of the Staphylococcus aureus gyrB-gyrA locus encoding the DNA gyrase A and B proteins.编码DNA促旋酶A和B蛋白的金黄色葡萄球菌gyrB-gyrA基因座的核苷酸序列。
J Bacteriol. 1992 Mar;174(5):1596-603. doi: 10.1128/jb.174.5.1596-1603.1992.
7
Minimal requirements of the Streptomyces lividans 66 oriC region and its transcriptional and translational activities.天蓝色链霉菌66 oriC区域的最低要求及其转录和翻译活性。
J Bacteriol. 1995 Aug;177(16):4765-71. doi: 10.1128/jb.177.16.4765-4771.1995.
8
Sequencing analysis reveals a unique gene organization in the gyrB region of Mycoplasma hominis.测序分析揭示了人型支原体gyrB区域独特的基因组织。
J Bacteriol. 1994 Sep;176(18):5835-42. doi: 10.1128/jb.176.18.5835-5842.1994.
9
Molecular characterization of the gyrB region of the oral spirochete, Treponema denticola.口腔螺旋体齿垢密螺旋体gyrB区域的分子特征分析
Gene. 2000 Aug 8;253(2):259-69. doi: 10.1016/s0378-1119(00)00254-7.
10
Nucleotide sequence of a Proteus mirabilis DNA fragment homologous to the 60K-rnpA-rpmH-dnaA-dnaN-recF-gyrB region of Escherichia coli.奇异变形杆菌DNA片段的核苷酸序列,该片段与大肠杆菌的60K-rnpA-rpmH-dnaA-dnaN-recF-gyrB区域同源。
Gene. 1990 Sep 1;93(1):27-34. doi: 10.1016/0378-1119(90)90131-a.

引用本文的文献

1
A highly processive actinobacterial topoisomerase I - thoughts on ' demand for an enzyme with a unique C-terminal domain.一种具有高延伸性的放线菌拓扑异构酶 I-关于“需要一种具有独特 C 末端结构域的酶”的思考。
Microbiology (Reading). 2020 Feb;166(2):120-128. doi: 10.1099/mic.0.000841. Epub 2019 Aug 7.
2
The heat shock protein 70 gene as a new alternative molecular marker for the taxonomic identification of Streptomyces strains.热休克蛋白70基因作为链霉菌菌株分类鉴定的一种新型替代分子标记。
AMB Express. 2018 Sep 10;8(1):144. doi: 10.1186/s13568-018-0674-4.
3
Molecular evaluation of antibiotic susceptibility: Tropheryma whipplei paradigm.
抗生素敏感性的分子评估:惠普尔嗜组织细胞菌范例
Antimicrob Agents Chemother. 2003 May;47(5):1658-64. doi: 10.1128/AAC.47.5.1658-1664.2003.
4
Sequence analysis of the gyrA and parC homologues of a wild-type strain of Vibrio parahaemolyticus and its fluoroquinolone-resistant mutants.副溶血性弧菌野生型菌株及其氟喹诺酮抗性突变体的gyrA和parC同源物的序列分析。
Antimicrob Agents Chemother. 1999 May;43(5):1156-62. doi: 10.1128/AAC.43.5.1156.
5
Sequence analysis, purification, and study of inhibition by 4-quinolones of the DNA gyrase from Mycobacterium smegmatis.耻垢分枝杆菌DNA回旋酶的序列分析、纯化及4-喹诺酮类药物对其抑制作用的研究。
Antimicrob Agents Chemother. 1996 Sep;40(9):2054-61. doi: 10.1128/AAC.40.9.2054.