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1)  Phoma wasabiae
山葵茎点霉
1.
Phoma wasabiae Yokogi,a pathogen wasabi black rot disease was isolated from wasabi in Sichuan, China and studied with PDA culture medium.
对山葵墨入病病株进行分离鉴定,明确其病原菌为山葵茎点霉菌(Phoma wasabiae Yokogi)。
2)  Wasabi roots
山葵根茎
1.
Study on storage and flavor producing conditions of Wasabi roots;
山葵根茎的贮藏及其风味物质产生条件的研究
3)  Phomopsis sp
拟茎点霉
1.
Composition Analysis on the Fatty Acid in a Strain of Endophytic Fungus of Phomopsis sp.
一株拟茎点霉属内生真菌脂肪酸成分分析
2.
The degradation of phenanthrene by Phomopsis sp.
对一株植物内生真菌拟茎点霉(编号B3)单独降解菲的条件及与水稻联合降解菲进行了研究。
3.
Bioncmics of shoot-blight in birch;
桦树枯枝病病原菌拟茎点霉Phomopsis sp。
4)  phoma
茎点霉
1.
One strain of filamentous fungi possessing stronger resistance and accumulation abilities was screened from mine soil and numbered as phoma sp.
从矿区土壤筛选到一株对镉具有较强抗性和富集能力的丝状真菌,编号为F2,根据其形态主要是分生孢子器的特征鉴定为茎点霉菌。
2.
Two new species and nine new records of Phoma and Phyllosticta from China are reported in this paper.
本文对采自东北地区的115份茎点霉(Phoma)和叶点霉(Phyllosticta)的标本进行分类研究,有新种2个和国内新记录种9个。
5)  Phoma herbarum
草茎点霉
1.
The Pathogenic Mechanism of Toxin from Phoma herbarum to Commelina communis;
草茎点霉毒素对鸭跖草致病相关生理反应的影响
2.
Effects of Environmental Factors on Effectiveness of Phoma herbarum Strain SYAU-06 against Commelina communis
环境因子对草茎点霉SYAU-06菌株侵染鸭跖草的影响
3.
Herbicidal Activity and Weeds Controlling Spectrum of Toxin from Phoma herbarum
草茎点霉粗毒素的除草活性和杀草谱研究
6)  Phomopsis
拟茎点霉
1.
Phomopsis anthurii a new species of Phomopsis;
拟茎点霉属一新种——花烛拟茎点霉
2.
Study on producing of β-conidia of Phomopsis in pure culture;
拟茎点霉乙型分生孢子形成的研究
3.
RAPD analysis of seventeen species of Phomopsis on fruit trees in Guangdong;
广东果树上17种拟茎点霉的RAPD分析
补充资料:茎点霉素
分子式:
CAS号:

性质:由茎点霉菌Fungus phoma,sp产生的多组分(A,B,B1,B2,C,D,E,F,G)的血小板活化因子拮抗剂。组分A:油状液体,旋光度[α]D+175°(c=0.75氯仿)。抑制血小板活化因子诱导的血小板凝聚的IC50值为1.0×10-5mol/L,抑制血小板活化因子同其受体结合的IC50值为2.3×10-6mol/L。组分B:熔点180~182℃,旋光度[α]D+146°(c=0.75,氯仿)。组分B1:无色结晶,熔点203~205℃,旋光度+167.3°(c=1.0,氯仿)。组分B2:无色油状,旋光度[α]D+173°(c=5.0,氯仿)。组分C:无色结晶,熔点204~205℃。组分D:无色结晶,熔点97~98℃,旋光度[α]D+114.3°(c=1.0,氯仿)。组分E:熔点148~149℃,旋光度+178.4°(氯仿)。组分F:熔点199~202℃,旋光度+120.9°(氯仿)。组分G:熔点131~132℃,旋光度+96.9°(氯仿)。组分B,B1,B2,C,D抑制血小板活化因子诱导的血小板凝聚的ICs0值分别为:17.0,9.8,1.6,6.4,0.8μmol/L,抑制血小板活化因子对受体结合IC50值分别为:>47.9,20.0,>22.1,63.0,0.12μmol/L。

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