Dynamism of cellulose synthases
Dynamism of cellulose synthases
批准号:
12490018
负责人:
HAYASHI Takahisa
金额:
$7.23万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (B)
财政年份:
2000
资助国家:
日本
项目状态:
已结题
起止时间:
2000 至 2001
中文摘要
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英文摘要
GhCesA2 is a cotton (Gossypium hirsutum) homolog of bacterial cellulose synthase gene that encodes cellulose 4-β-glucosyltransferase. The central catalytic region of GhCesA2 was expressed as a soluble protein in methylotrophic yeast Pichia pastoris. The molecular size of the recombinant protein was 100 kDa, which decreased to 85 kDa after the treatment with endoglycosidase H. The recombinant GhCesA2 catalyzed transfer of glucose from UDP-glucose into unknown products in the presence of the extract of cotton hypocotyls, but the products were not β-1,4-glucan. The putative cotton (Gossypium Hirsutum L.) cellulose synthase gene GhCesA2was expressed in insect cells using baculovirus systems and the hydrodynamic properties of the gene product were determined in its native state. The recombinant protein could be solubilized with 1% Triton X-100 from the membrane fraction of infected Sf9 cells. The results obtained from gel filtration chromatography and H_2O/D_2O sucrose gradient sedimentatio … More n showed that the recombinant GhCesA2 had two types in size. We calculated the partial specific volume, Stokes radius and molecular weight of the protein-detergent complex and estimated the molecular weight of the two proteins as 142,000 and 285,000. The result suggested that the recombinant GhCesA2 form a homo-dimer.Three-dimensional structure of cellulose synthase remains difficult because none of purification and crystallization procedures for its recombinant protein has not been established. In this study, we succeeded in expressing a Histidine-tagged BcsA.(subunit A of a bacterial cellulose synthase) using a bacurovirus expression system in SF9 cells. The expression of this recombinant protein was assessed and verified by SDS-PAGE and western blotting, and found promissing for mass production by purifying them with His tags. We are now stepping in the next stage to measure more precisely the proteins, for instance, the activity as well as the size distribution either by electron microscopy and X-ray small angle scattering. Less
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T. Konishi, F. Sakai and T. Hayashi: "Functional analysis of cellulose-synthase-like genes"International Congress Series. 449. 75-78 (2001)
T. Konishi、F. Sakai 和 T. Hayashi:“纤维素合酶样基因的功能分析”国际大会系列。
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T.Hayashi: "Gene for cellulose synthase and the gene product"Cellulose, Asakura Publishers. 48-59 (2000)
T.Hayashi:“纤维素合酶基因及其基因产物”纤维素,朝仓出版社。
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Y.Ohmiya,M.Samejima,T,Hayashi: "Evidence that endo-1,4-β-glucanases act on cellulose in suspension-cultured polar cells"The Plant Journal. 24・2. 147-158 (2000)
Y. Ohmiya、M. Samejima、T、Hayashi:“内切 1,4-β-葡聚糖酶作用于悬浮培养的极细胞中的纤维素的证据”《植物杂志》24・2(2000 年)。
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T.Konishi, T.Nakai, F.Sakai., T.Hayashi: "Formation of callose from sucrose in cotton fiber microsomal membranes"J. Wood Sci.. 46. 1-7 (2001)
T.Konishi、T.Nakai、F.Sakai.、T.Hayashi:“棉纤维微粒体膜中蔗糖形成胼胝质”J。
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Y. Ihara, F. Sakai and T. Hayashi: "Transferase activity of GhCesA2 (putative cotton cellulose 4-β-glucosyltransferase) expressed in Pichia pastoris"J. Wood Sci.. (in press).
Y. Ihara、F. Sakai 和 T. Hayashi:“毕赤酵母中表达的 GhCesA2(假定的棉花纤维素 4-β-葡萄糖基转移酶)的转移酶活性”J. Wood Sci.(出版中)。
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共 16 条
Function of xyloglucan in the poplar xylem
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批准号:23380104
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项目类别:Grant-in-Aid for Scientific Research (B)
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资助金额:$10.65万
-
财政年份:2011
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负责人:HAYASHI Takahisa
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依托单位:
Transgenic trees for field trial in the world
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批准号:19405030
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项目类别:Grant-in-Aid for Scientific Research (B)
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资助金额:$6.82万
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财政年份:2007
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负责人:HAYASHI Takahisa
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依托单位:
Field trial of transgenic poplars for industrial use
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批准号:19208016
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项目类别:Grant-in-Aid for Scientific Research (A)
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资助金额:$30.28万
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财政年份:2007
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负责人:HAYASHI Takahisa
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依托单位:
Molecular cloning of xyloglucanase in suspension-cultured poplar cells
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批准号:04455016
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项目类别:Grant-in-Aid for General Scientific Research (B)
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资助金额:$4.16万
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财政年份:1992
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负责人:HAYASHI Takahisa
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依托单位: