殺蟲晶體蛋白 的英文怎麼說

中文拼音 [shāchóngjīngtǐdànbái]
殺蟲晶體蛋白 英文
insecticidal crystal protein
  • 殺 : Ⅰ動詞1 （使失去生命; 弄死） kill; slaughter 2 （戰斗） fight; go into battle 3 （削弱; 消除） wea...
  • 蟲 : 名詞1. （蟲子） insect; worm 2. （姓氏） a surname
  • 晶 : Ⅰ形容詞（光亮） brilliant; glittering Ⅱ名詞1. （水晶） quartz; （rock） crystal 2. （晶體） any crystalline substance
  • 體 : 體構詞成分。
  • 蛋 : 名詞1. （鳥類或龜、蛇類所產的卵） egg 2. （像蛋形的東西） an egg-shaped thing 3. （辱罵之詞）
  • 白 : Ⅰ形容詞1 （似雪的顏色） white 2 （清楚; 明白; 弄明白） clear 3 （空的; 沒加他物的） pure; clear; ...
  • 晶體 : [晶體學] crystal; vitrella; crystal body; crystalloid; x-tal
  • 蛋白 : 1. （卵中透明的膠狀物質） egg white; albumen; gary2. [生物化學] （蛋白質） protein
  1. Two main parts were included in the present thesis. part i. cloning and expression cryigenes of bacillus thuringiensis in different host strains

    一、蘇雲金芽胞桿菌殺蟲晶體蛋白基因在不同受體菌中的表達1
  2. Detection and bio - assay of insecticidal crystal protein bmb20 - 4 from bacillus thuringiesis

    4的殺蟲晶體蛋白檢測及毒力測定
  3. Analysis of insecticidal crystal protein and its cry - type genes of bacillus thuringiensis isolates from china

    分離株殺蟲晶體蛋白及基因分析
  4. These insecticidal proteins are commonly known as insecticidal crystal proteins ( icp ) or delta endotoxin

    這些殺蟲蛋白通稱為殺蟲晶體蛋白（ icp ）或-蛋白。
  5. Most susceptible insects are killed by ingestion of the crystals alone ; a mixture of spores and crystals are required for a toxic effect in only a small number of insects

    大多數易感蟲種只要攝取晶體蛋白即可被殺死；只有一小部分昆蟲要求孢子和晶體同時存在。
  6. 3. construction of fusion genes with insecticidal protein gene and gfp the fusion genes was constructed by pcr. the pesticidal crystal protein gene crylac10 and gfp were chosen to construct the fusion genes

    建殺蟲晶體基因與gfp基因的融合基因pcr擴增全長gfp片段融合於去掉終止結構的殺蟲晶體蛋白基因的c -端，構建融合基因。
  7. The results of sequencing and structural analysis showed that the gene, named crylaa14 by international nomenclature committee of bt 5 - endotoxin, was 3552 bp and the open reading frame encoded a 133. 7 kda protein with 1183 amino acids

    序列測定結果表明該基因編碼區為3552bps ，編碼1183個氨基酸，分子量為133 . 7kda ，等電點為pi4 . 755 。該基因序列已在genbank注冊， accessionnumber為ay197341 ，並被國際bt殺蟲晶體蛋白基因命名委員會正式命名為cry1aa14 。
  8. The research results are summarized as following : 1. the relationship between gene types and the toxicity against s. exigua in order to construct satisfactory genetically engineered strain, it is first necessary to understand the relationship between gene types and the toxicity. nine strains containing crylc were chosen for study for this purpose

    研究結果總結如下： 1菌株對甜菜夜蛾的毒力與基因類型的關系pcr擴增檢測了九個蘇雲金芽胞桿菌菌株所含殺蟲晶體蛋白（ insecticidalcrystalprotein ， icp ）基因，根據擴增結果將它們分為5種基因類型。
  9. The recombinant plasmids pbmb121l, pbmb9821l and pbmb986l were constructed after transferring bacillus thuringiensis icps gene crylaal, crylaclo and crylca from their original plasmid vectors to different plasmid vector. the relevant recombinant strains were obtained after introducing the 3 recombinant plasmids into bacillus thuringiensis plasmid - free mutant strain 8mb 171 by electroporation. the transformation and expression properties of 8mb 171 were studied

    通過將蘇雲金芽胞桿菌殺蟲晶體蛋白基因cry1aal 、 cry1ac10和cry1ca轉移至不同質粒載體上，分別構建了重組質粒pbmb121l 、 pbmb9821l和pbmb986l ，並分別導入無質粒突變株bmb171 ，篩選得到攜帶相應icps基因的重組菌株。
  10. 4. effect of resolution vector on the expression of pesticidal crystal protein genes this work successfully introduced pesticidal crystal protein genes into crystal negative strain bmb171 by using resolution shuttle vectors. after resolution, the expression of cry1ac and cry 1c genes have no obvious change, but the expression of cry3a genes has great increase in the same condition

    解離反應對殺蟲晶體蛋白基因表達的影響成功地利用解離載體將crylac10 ， crylc和cry3a基因導入蘇雲金芽胞桿菌無晶體突變株， crylac和crylc基因解離前後的表達量和殺蟲毒力未見明顯變化， cry3a基因在相同條件下則表達量有所提高，至於為何只對基因cry3a有作用尚不清楚，國內外也未見有人作相關報道。
  11. Microcalorinetric study on b. thuringiensis by using an lkb - 2277 bioacitivity monitor, the thermogenic curves of different b thuringiensis strains ybt - 833 and ybt - 833 - 2 - i, have been determined. the metabolism heat output revealed the heat output was correlated to the yield of the protein, the higher yield protein, the less heat output. a microcalorimetric technique based on the bacterial heat - output was explored to evaluate the effect of various promoters and different plasmid original replicons on the expression of gfp

    不同蘇雲金芽胞桿菌基因工程菌的微量熱變化利用生物活性檢測器lkb - 2277研究殺蟲晶體蛋白含量不同的兩株菌ybt - 833 、 ybt - 833 - 2 - 1的熱動力學變化，發現菌體合成殺蟲晶體蛋白的過程是一個耗能的過程，殺蟲晶體蛋白產量高的菌株向外釋放的代謝熱少，反之亦然。
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