枯草隆 的英文怎麼說

中文拼音 [kūcǎolōng]
枯草隆 英文
chloroxifenidium; chloroxuron; norex; tenoran
  • 枯 : 形容詞1 （植物等失去水分; 乾枯） （of a plant etc ） withered 2 （井、河流等變得沒有水） （of a w...
  • 草 : Ⅰ名詞1 （草本植物的統稱） grass 2 （指用作燃料、飼料等的稻、麥之類的莖和葉） straw 3 （草稿） dra...
  • 隆 : 隆Ⅰ形容詞1 （盛大） grand2 （興盛） prosperous; flourishing; thriving 3 （深厚; 程度深） deep; in...
  1. Used as 1. 1094 strain of bacillus subtilis as researched material, the structural genes of biotin operon ( bio operon ) were cloned, and its sequence were engineered

    本研究以枯草桿菌asl . 1094菌株為研究材料，克隆了生物素操縱子基因，並對基因序列進行改造。
  2. Contrasting analysis with the genes sequence of bacillus subtilis 168 strain ' s bio operon, the sequence of bio operon of as 1. 1094 strain had 12 bases difference with that of 168 train, and 7 bases caused variation of amino acid

    1094菌株與168菌株bioafdb基因序列完全一致， 9個差異堿基是由於pcr擴增導致的。枯草桿菌生物素操縱子基因4個亞克隆序列的測序結果證實， asi
  3. 2. cloning of structural genes of bacillus subtilis bio operon diluted the genomic dna of bacillus subtilis as the template, long pcr product ( 10. 3kb ) and three salvage pcr products were separately gained by optimization of reaction conditions of pcr

    枯草桿菌生物素操縱子基因的克隆將枯草桿菌基因組dna稀釋后，通過pcr反應條件的優化，分別擴增得到了生物素操縱子基因的長距離pcr產物（ 10 . 3kb ）和3個分段pcr產物。
  4. The expression plasmid called psugv - badfe was constructed by inserting ba - dfe gene into e. coli - b. subtilis shuttle vector psugv4 and the

    將ba0fe基因克隆到大腸桿菌一枯草桿菌穿梭載體psugv4中，得到重組質粒psugv badfe ，然後轉化到枯草桿菌wb600中進行了分泌表達。
  5. 3. the cloning of a - amylase gene : the methods of shotgun, pcr and rt - pcr were selected to clone a - amylase genes from bacillus subtilis hn503, xanthomonas campestris pv. campestris 8004 and aspergillus oryzae, hn504 the recombinant plasmid with cloned gene was designated as phn504, phn503 and phn8004

    本研究分別選用了鳥槍克隆法、 pcr和rt - pcr克隆法，成功地克隆到枯草芽胞桿菌（ bacillussubtilis ） hn503 、野油菜黃單胞菌（ xanthomonascampestrispvcampestris ） 8004和米麴黴（ aspergillus口盡留『 ） hn504的價澱粉酶基因。
  6. The sacvgb gene was then cloned into e. coli - - b. sublilis shuttle vector psugv4 and a recombinant plasmid named psu - sacvgb was constructed. after transformation with b. sublilis wb600, the transformants successfully produced vhb intracellularly. the influence of vhb on b. subtilis is under investigation

    將sacvgb基因克隆到大腸桿菌-枯草桿菌穿梭載體psugv4中，獲得重組表達質粒psu - sacvgb ，然後轉化枯草桿菌wb600 ，轉化子經2蔗糖誘導，該基因在枯草桿菌中表達。
  7. Four colonies of transformed e. coli dh5 a with clear hydroiyzing zone on the chitin agar were obtained. the gene fragment in these isolates was identified by the methods of plasmid processing. dna sequencing analysis showed that sequence homology between pcr fragment and chromosomal dna of b. subtilis from 2599451 to 2812870 was 85 %, and was 30 % between the fragment and the genes encoding for chitinase of bacillus ( including b. subtilis ) in genebank

    測序並序列比較結果表明該基因片段同已發表的枯草芽孢桿菌幾丁質酶和內切葡聚糖酶編碼幕因的克隆及重組芽抱桿菌的構建glyb一apre之間的同源性是最高的，為35 % ;同bacz 』了了ussp . bp23ce1b 、 b . p朋刀us內切葡聚糖酶和b . pol理vxap一1 ， 4一內切葡聚糖酶的編碼基因的同源性只有27 % 。
分享友人
分享到 Line

分享到臉書