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蛋白米
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  protein rice
     It included low amylose and protein material' s selection in early generation, low protein rice culture, purchase according to quality, paddy and brown rice choiceness and super low temperature store.
     包括低直链淀粉及蛋白质含量材料的早期筛选,低蛋白米栽培,分品质收购,稻谷精选,糙米色选,超低温贮藏技术等。
短句来源
  相似匹配句对
     THE TECHNICAL METHOD FOR PREPARATION OF PHYIC ACID AND ORYZENIN
     植酸和蛋白的制备工艺
短句来源
     Research on the Processing of Amino Acid Beverage from Rice Residue Protein
     利用蛋白制备氨基酸饮料
短句来源
     Western blotting tested the expressed proteins.
     蛋白表达。
短句来源
     RADIOIMMUNOASSAY OF F PROTEIN
     F蛋白的放射免疫分析
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     72 METPA
     《72
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  protein rice
The possible use of this line as a low protein rice cultivar is discussed.
      
Silicalite zeolite : A novel matrix for purification and estimation of a hydrophobic protein rice prolamin
      
Effect of zinc supplementation and high-protein rice on the growth of preschool children on a rice-based diet
      
Supplementation of this diet with 5 mg zinc and substitution of high-protein (10.4%) rice for average-protein rice (~~7.4%) together resulted in significantly faster height and weight increases in the experimental group than in the control group.
      
Effect of high protein rice on nitrogen retention and growth of preschool children on a rice-based diet
      
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B_(625), proteinase from P. aeuginase purified by DEAE-cellulose chromatography showed a single band in SDS-polyacrylamide gel electrophoresis and had a maximum absorption at 275nm. Its molecular weight was about 34000 Dalton estimated by disc gel electrophoresis. The enzyme consisted of 323 amino acid residues by calculation, in which cystine or cysteine residues was absent.

经DEAE纤维素柱层析提纯的B_(625)蛋白酶,在SDS聚丙烯酰胺凝胶电泳上呈一条带。盘电泳测定表明,其分子量约为34000道尔顿。根据计算,酶分子由323个氮基酸组成,不合有半胱氨酸或胱氨酸。酶蛋白的紫外吸收光谱最大吸收为275毫微米。酶作用于酪蛋白和血清白蛋白的米氏常数(K_(198))分别为6.7×10~(-3)和7.1×10~(-2)克/毫升。酶对酪蛋白的水解能力大于碱性蛋白酶(地衣芽胞杆菌)或弗氏链霉的蛋白酶。色氨酸的修饰剂NBS强烈地抑制酶活力。SDS和Triton X-100对酶活力亦有一定抑制作用。

Degradation characteristics of fenvalerate by the isolated strain YF11 and its enzyme was determined.At biomass of 0 20(OD 415nm )in pure culture system,degradation kinetics of >30mg/L of fenvalerate was considered to fit zero order model,their rates were range of 1 876 to 2 124mg/(L·h).The rate was obviously inhibited by >200mg/L of fenvalerate.It was found that the degradation rates of fenvalerate had a similar direct relationship to the biomass of strain YF11 at same concentration of fenvalerate.The...

Degradation characteristics of fenvalerate by the isolated strain YF11 and its enzyme was determined.At biomass of 0 20(OD 415nm )in pure culture system,degradation kinetics of >30mg/L of fenvalerate was considered to fit zero order model,their rates were range of 1 876 to 2 124mg/(L·h).The rate was obviously inhibited by >200mg/L of fenvalerate.It was found that the degradation rates of fenvalerate had a similar direct relationship to the biomass of strain YF11 at same concentration of fenvalerate.The degradation curve at 10mg/L of fenvalerate was considered to fit first order model.Optimum activity of cell free enzyme from strain YF11 occurred at condition of 32 5℃ and pH 8 0.The maximum enzymatic degradation rate of fenvalerate and its K m were 211 8nmol/(min·mg) of protein and 41 4nmol/ml,respectively.

测定了降解菌YF11及其胞内酶对杀灭菊酯的降解特性.在纯培养系统中,菌量为OD415nm0.20时,YF11对大于30mg/L的杀灭菊酯的降解呈零级动力学特征,浓度为30-100mg/L时,降解速率为1.876—2.124mg/(Lh);浓度大于200mg/L的杀灭菊酯对降解菌YF11的降解产生抑制作用.降解速率与菌量近似成正比关系;10mg/L杀灭菊酯的降解曲线呈一级动力学特征.从YF11提取的粗酶液在32.5℃、pH8.0时对杀灭菊酯显示最大的降解活性,其最大降解速率为211.8nmol/(minmg蛋白)、米氏常数(Km)为41.4nmol/ml

An extracellular proteinase from Candida albicans WD27 was purified by (NH4)2SO4 fractionation and DEAE-Sephacel ion-exchange chromatography with 25.4 fold and 5.2% yield. This enzyme appeared to be aspartic proteinase since the enzyme activity could be inhibited by pepstatin which was specific inhibitor of this class of proteinase. The enzyme had an acidic proteolytic activity profile with the optimum pH of 4.0. The optimum temperature of the enzyme activity was 37℃. The proteinase had a broad substrate specificity...

An extracellular proteinase from Candida albicans WD27 was purified by (NH4)2SO4 fractionation and DEAE-Sephacel ion-exchange chromatography with 25.4 fold and 5.2% yield. This enzyme appeared to be aspartic proteinase since the enzyme activity could be inhibited by pepstatin which was specific inhibitor of this class of proteinase. The enzyme had an acidic proteolytic activity profile with the optimum pH of 4.0. The optimum temperature of the enzyme activity was 37℃. The proteinase had a broad substrate specificity with the highest susceptibility to bovine hemoglobin. The Km for bovine hemoglobin was determined to be 0.814mmol/L.

利用硫酸铵分级沉淀和DEAE-Sephacel离子交换层析从白色念珠菌WD27培养液中提纯得到一种蛋白酶,纯化倍数为25.4,收率为5.2%。其活性可被抑胃肽特异抑制,初步鉴定该酶为天冬氨酸蛋白酶。该酶在酸性范围内有水解蛋白活性,最适作用pH为4.0,最适温度为37℃。酶在pH5.0~6.0、45℃以下较稳定,该酶具有较广的底物作用范围,对牛血红蛋白最敏感。酶作用于牛血红蛋白的米氏常数Km为0.814mmol/L。

 
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