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   氨基酸掺入 的翻译结果: 查询用时:0.017秒
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氨基酸掺入
相关语句
  amino acid incorporation
     Effect of Arginine Vasopressin_(4-9) Peptide on the Amino Acid Incorporation in Synaptosome of Aged Rat Brain
     8精氨酸加压素_(4-9)肽对衰老脑突触体氨基酸掺入的影响
短句来源
     INHIBITION ON AMINO ACID INCORPORATION OF MICROSOME BY CADMIUM, MERCURY AND LEAD
     镉、汞、铅在体内对氨基酸掺入微粒体的特异性抑制作用
短句来源
     EFFECTS OF CADMIUM, LEAD AND MERCURY ON AMINO ACID INCORPORATION INTO MICROSOMAL PROTEIN IN VITRO
     镉、铅、汞在体外对氨基酸掺入微粒体蛋白中的影响
短句来源
  “氨基酸掺入”译为未确定词的双语例句
     Hepatic microsomes from untreated rats, energy system of protein synthesis, labelled amino acids and cadmium, lead and mercury respectively, were incubated in vitro to observe the effects of these metals on ami-no acid incorporation into microsomal protein.
     将从未经处理大鼠体内分离出来的肝微粒体与蛋白合成能量系统,同位素标记氨基酸以及各种浓度镉、铅、汞在体外一起温育以测定镉、铅、汞对氨基酸掺入微粒体蛋白中的影响.
短句来源
     High molecular weight virus ENA stimulates the incorporation of radioactive amino acids into protein in a reticulooyte cell free system.
     高分子病毒RNA在网织红细胞无细胞系统中刺激放射性氨基酸掺入
短句来源
     The open reading frame of gH was inserted into pET 3CP then transfered to E. coli ,BL21 ,PLYS S and PLYS E strains. The expression of gH was seen by 35S-Methionine incorporation assay.
     35S甲硫氨基酸掺入试验表明,带有部分HHV-6gH基因片段的pET3CP质粒,可在上述大肠杆菌株表达,分子量约为37×10~3。
短句来源
     It was found by the experiment of protein in vivo synthesis that the in corporation of labeled amino acid in infected leaves in high temperature increased to 1.51 times of that in infected leaves in normal temperature, and to 1.42 times of that in uninoculated control in higher temperature respectively .
     蛋白质体内合成试验发现接种苗移入高温下处理24 h 后,接种叶中标记氨基酸掺入率分别增至未经高温处理的接种叶的1.51 倍和高温处理的未接种叶的1.42 倍。
短句来源
  相似匹配句对
     CHEMICAL SYNTHESIS OF AMINO ACIDS
     氨基酸的化学合成
短句来源
     biosynthesis of amino acids;
     氨基酸的生物合成;
短句来源
     INHIBITION ON AMINO ACID INCORPORATION OF MICROSOME BY CADMIUM, MERCURY AND LEAD
     镉、汞、铅在体内对氨基酸掺入微粒体的特异性抑制作用
短句来源
     EFFECTS OF CADMIUM, LEAD AND MERCURY ON AMINO ACID INCORPORATION INTO MICROSOMAL PROTEIN IN VITRO
     镉、铅、汞在体外对氨基酸掺入微粒体蛋白中的影响
短句来源
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  amino acid incorporation
The pathways of myofibrillar assembly and degradation were studied in normal heart and during developing hypertrophy by two independent methods: amino acid incorporation kinetics and the double isotope technique.
      
A simple method is described to test amino acid incorporation into human leukocytes.
      
Higher protein concentration, both in high-protein stocks and in IR-8 grown at 120 kgN/ha, was associated with increased levels of: soluble amino nitrogen, GDH activity, 3H-uridine and 14C-amino acid incorporation.
      
The rate of amino acid incorporation was measured in both liver and kidney extracts with14C-leucine, lysine, serine, or glycine as labels.
      
The effects of insulin on net glycogen synthesis and amino acid incorporation into protein were studied in cultured hepatocytes from adult normal and alloxan diabetic rats.
      
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Nitrate reductase (NADH: NR, EC 1. 6. 6. 1) activity of the detached leaves of etiolated rice seedlings was induced in low pH and dark condition. In the range of pH 3.0 to pH 7.0, NR activity increased as the pH of induction solution decreased. The maximal activity was obtained at pH 3.0. At pH 7.0, no activity was detected in the presence or absence of KNO_3. There was a lag period of about 2h before the activity appeared, and cycloheximide (CHI, 5 ppm) or tungstate (25 mmol/L) completely blocked NR activity...

Nitrate reductase (NADH: NR, EC 1. 6. 6. 1) activity of the detached leaves of etiolated rice seedlings was induced in low pH and dark condition. In the range of pH 3.0 to pH 7.0, NR activity increased as the pH of induction solution decreased. The maximal activity was obtained at pH 3.0. At pH 7.0, no activity was detected in the presence or absence of KNO_3. There was a lag period of about 2h before the activity appeared, and cycloheximide (CHI, 5 ppm) or tungstate (25 mmol/L) completely blocked NR activity induction by low pH and KNO_3. The incorporation of H~3-Leu, H~3-Ala and H~3-Glu into NR protein was about twice as high at pH 3.0 as at pH 7.0, showing that the amount of NR and the rate of NR de novo synthesis were different between pH 3.0 and pH 7.0 treatment.In the condition of low pH and darkness, benzyladenine (BA, 5 ppm) and abscisic acid (ABA, 15 ppm) enhanced NR activity by about 30% and 80% respectively. Neither BA nor ABA could replace the role of low pH in the induction of NR activity in the dark. In the presence of CHI (1 ppm), BA exhibited promoting effect on the activity. In contrast with BA, ABA reinforced the inhibitory effect of CHI on NR activity, suggesting that BA differs from ABA in the mechanism of NR activity promotion. In the condition of pH 7.0 and light, ABA inhibited the induction of NR activity.

在低pH条件下,水稻离体黄化叶片的硝酸还原酶(NR)活性能在暗中诱导产生,其诱导过程约有2h的滞后期,亚胺环已酮(CHI,5ppm)和Na_2WO_4(25 mmol/L)能完全抑制这种诱导作用。在最适pH 3.0时,H~3标记氨基酸掺入NR的量比pH 7.0时约高2倍,表明酶活性的产生与酶蛋白的重新合成有关。 当低pH暗诱导时,BA(5ppm)和ABA(15ppm)能使酶活性分别提高约30%和80%,但它们都不能取代低pH在NR活性暗诱导中的作用。当存在1ppm CHI的时候,BA仍促进NR活性,而ABA则加强CHI对酶活性的抑制作用,这提示BA与ABA在低pH暗诱导条件下促进NR活性的机制是不同的。在pH 7.0的光诱导条件下,ABA对NR活性起抑制作用。

Hepatic microsomes from untreated rats, energy system of protein synthesis, labelled amino acids and cadmium, lead and mercury respectively, were incubated in vitro to observe the effects of these metals on ami-no acid incorporation into microsomal protein. The results showed that the amino acid incorporation could be inhibited by all three metals with dose-effect dependence.

将从未经处理大鼠体内分离出来的肝微粒体与蛋白合成能量系统,同位素标记氨基酸以及各种浓度镉、铅、汞在体外一起温育以测定镉、铅、汞对氨基酸掺入微粒体蛋白中的影响.实验结果表明,上述三种金属都抑制氨基酸向肝微粒体蛋白中的掺入.随着这些金属在体外浓度的增加,此种抑制作用,也越明显.

SES mouse leukemia virus (SESV) was obtained from the culture medium supernatant of infected NIH 3T3 mouse fibroblasts. SESV ENA was prepared from fresh viral pellets. ENAs of various fractions were determined by sedimentation coefficient followed by gel eleotrophoresis. The components of SESV ENA consist of two main fractions, one sedimenting at about 60 -70S (after treatment with heat at about 35S), plus small amounts of ENA sedimenting in the 18S and 28S areas, and the other at 4 -6S. High molecular weight...

SES mouse leukemia virus (SESV) was obtained from the culture medium supernatant of infected NIH 3T3 mouse fibroblasts. SESV ENA was prepared from fresh viral pellets. ENAs of various fractions were determined by sedimentation coefficient followed by gel eleotrophoresis. The components of SESV ENA consist of two main fractions, one sedimenting at about 60 -70S (after treatment with heat at about 35S), plus small amounts of ENA sedimenting in the 18S and 28S areas, and the other at 4 -6S. High molecular weight virus ENA stimulates the incorporation of radioactive amino acids into protein in a reticulooyte cell free system. Analysis of the translational products demonstrated the synthesis of at least three proteins corresponding in molecular weight to several authentic viral proteins.

从感染小鼠腹水瘤病毒(SRSV)的NIH3T3小鼠成纤维细胞培养液中,分离SRSV,并提取病毒核酸(SRSV RNA),通过超速离心和凝胶电泳测定RNA的沉降系数和分子量。SRSV RNA主要由两部分组成:①沉降系数(8)约60~70S(热处理后约35S)及少量18S和28S;②是4~5S。高分子病毒RNA在网织红细胞无细胞系统中刺激放射性氨基酸掺入。对翻译产物分析表明:至少有3个蛋白的分子量相应于病毒蛋白。

 
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