Joint Research on Myxobacterial Development
Joint Research on Myxobacterial Development
批准号:
10044213
负责人:
KOMANO Teruya
金额:
$2.88万
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (B).
财政年份:
1998
资助国家:
日本
项目状态:
已结题
起止时间:
1998 至 2000
中文摘要
粘细菌是一种独特的革兰氏阴性细菌,它经历多细胞发育。当营养物质在固体培养基中耗尽时,细胞聚集形成丘,最终转化为子实体。杆状细胞分化为圆形或卵圆形孢子。在黄色粘球菌的发育过程中,已知发生五个细胞间信号交换循环。的fruA基因编码一个假定的25 kDa的转录因子,黄曲霉的发展必不可少的。在本研究中,我们已经证明了存在一个假定的阻遏物X的fruA表达的凝胶迁移实验。结合竞争实验表明X识别序列。通过质谱分析蛋白质P15的结构,蛋白质P15的表达被fruA突变抑制。在ORF134中插入卡那霉素抗性DNA片段导致发育失败,这表明ORF134-fruB操纵子的存在负责黄曲霉的发育。两个启动子结构被发现这个操纵子:一个启动子在营养生长过程中工作,而两个启动子在发育过程中工作。发现M.xanthus lonD是一个热激基因。lonD的表达不依赖于编码大肠杆菌RpoH同源物的sigBCE基因,但依赖于编码RpoD同源物的hsfA和sigA。hsfA基因编码一个假定的效应的双组分系统,这是磷酸化的HsfB激酶。磷酸化的HsfA与lonD基因的启动子序列结合。黄色分枝杆菌携带至少13种真核样蛋白Ser/Thr pkn激酶。通过双杂交实验发现许多基因产物与Pkn激酶相互作用。
英文摘要
Myxobacteria are unique gram-negative bacteria which undergo multicellular development. When nutrients are depleted in a solid medium, cells aggregate to form mounds which eventually convert to fruiting bodies. Rod-shaped cells differentiate to round or ovoid spores. During the development of Myxococcus xanthus, five cycles of intercellular signal exchanges are known to occur. The fruA gene encodes a putative 25-kDa transcription factor essential for the development of M.xanthus. In the present study, we have demonstrated the presence of a putative repressor X for fruA expression by gel shift experiments. Binding competition experiments suggested the X recognition sequence. Structure of protein P15, expression of which was inhibited by the fruA mutation, was analyzed by mass spectroscopy. Insertion of kanamycin-resistance DNA fragment into ORF134 resulted in failure of development, suggesting the presence of ORF134-fruB operon responsible for M.xanthus development. Two promoter structures were found for this operon : One promoter works during vegetative growth, while both two promoters work during development. M.xanthus lonD was found to be a heat shock gene. Expression of lonD was independent on sigBCE genes encoding an Escherichia coli RpoH homolog, but dependent on hsfA and sigA encoding a RpoD homolog. The hsfA gene encodes a putative effecter of a two-component system, which was phosphorylated by HsfB kinase. Phosphorylated-HsfA bound to promoter sequence for lonD gene. M.xanthus carries at least 13 eukaryotic-like protein Ser/Thr pkn kinases. Many gene products were found to interact with Pkn kinases by two-hybrid experiments.
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Yamanaka, K., M.Inouye, and S.Inouye: "Identification and characterization of five cspA homologous genes from Myxococcus xanthus."Biochim.Biophys.Acta.. 1447. 357-365 (1999)
Yamanaka, K.、M.Inouye 和 S.Inouye:“来自 xanthus 粘球菌的五个 cspA 同源基因的鉴定和表征。”Biochim.Biophys.Acta.. 1447. 357-365 (1999)
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Komano, T., T.Yoshida, K.Narahara, and N.Furuya: "The transfer region of IncI1 plasmid R64 : similarities between R64 tra and Legionella icm/dot genes."Mol.Microbiol.. 35. 1348-1359 (2000)
Komano, T.、T.Yoshida、K.Narahara 和 N.Furuya:“IncI1 质粒 R64 的转移区域:R64 tra 和军团菌 icm/dot 基因之间的相似性。”Mol.Microbiol.. 35. 1348-1359 (
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Yoshida, T., N.Furuya, M.Ishikura, T.Isobe, K.Haino-Fukushima, T.Ogawa, and T.Komano: "Purification and characterization of thin pili of IncI1 plasmids ColIb-P9 and R64 : formation of PilV-specific cell aggregates by type IV pili."J.Bacteriol.. 180. 2842-
Yoshida, T.、N.Furuya、M.Ishikura、T.Isobe、K.Haino-Fukushima、T.Okawa 和 T.Komano:“IncI1 质粒 ColIb-P9 和 R64 薄菌毛的纯化和表征:形成
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Ishiwa, A., and T.Komano: "The lipopolysaccharide of recipient cells is a specific receptor for PilV proteins, selected by shufflon DNA rearrangement, in liquid matings with donors bearing the R64 plasmid."Mol.Gen.Genet.. 263. 159-164 (2000)
Ishiwa, A. 和 T.Komano:“受体细胞的脂多糖是 PilV 蛋白的特异性受体,通过洗牌 DNA 重排选择,与带有 R64 质粒的供体进行液体交配。”Mol.Gen.Genet.. 263。
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Koiwai, H., S.Akaba, M.Seo, T.Komano, and T.Koshiba: "Functional expression of two Arabidopsis aldehyde oxidases in the yeast Pichia pastoris."J.Biochem.. 127. 659-664 (2000)
Koiwai, H.、S.Akaba、M.Seo、T.Komano 和 T.Koshiba:“酵母毕赤酵母中两种拟南芥醛氧化酶的功能表达。”J.Biochem.. 127. 659-664 (2000)
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共 37 条
Mechanism of conjugal transfer in IncI plasmids
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批准号:17570007
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$2.18万
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财政年份:2005
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负责人:KOMANO Teruya
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依托单位:
Mechanism of conjugal transfer in plasmid R64
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批准号:14540568
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$2.56万
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财政年份:2002
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负责人:KOMANO Teruya
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依托单位:
Analysis of transfer genes of incompatibility group I plasmids
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批准号:11640622
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$2.24万
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财政年份:1999
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负责人:KOMANO Teruya
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依托单位:
Cleavage and Rejoining of DNA in the Shufflon-Specific Recombinase
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批准号:10216207
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项目类别:Grant-in-Aid for Scientific Research on Priority Areas
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资助金额:$24.06万
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财政年份:1998
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负责人:KOMANO Teruya
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依托单位:
Analysis of transfer genes in plasmid R64
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批准号:06454005
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项目类别:Grant-in-Aid for Scientific Research (B)
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资助金额:$4.48万
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财政年份:1994
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负责人:KOMANO Teruya
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依托单位:
Analysis of Conjugal Transfer Region of Plasmid R64.
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批准号:03640541
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项目类别:Grant-in-Aid for General Scientific Research (C)
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资助金额:$1.22万
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财政年份:1991
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负责人:KOMANO Teruya
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依托单位:
Analyses of Clustered Inversion Region in Incl Plasmids.
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批准号:01540533
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项目类别:Grant-in-Aid for General Scientific Research (C)
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资助金额:$1.15万
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财政年份:1989
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负责人:KOMANO Teruya
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依托单位:
国内基金
海外基金
水稻边界发育缺陷突变体abnormal boundary development(abd)的基因克隆与功能分析
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批准号:32070202
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项目类别:面上项目
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资助金额:58.0万元
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批准年份:2020
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负责人:汪泉
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依托单位:
Development of a Linear Stochastic Model for Wind Field Reconstruction from Limited Measurement Data
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项目类别:--
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资助金额:40万元
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批准年份:2020
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负责人:Vikrant Gupta
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依托单位: