操縱子基因 的英文怎麼說

中文拼音 [cāozōngzijīyīn]
操縱子基因 英文
operon gene
  • 操 : Ⅰ動詞1 （抓在手裡; 拿; 掌握） hold; grasp 2 （做; 從事） act; do; operate 3 （用某種語言、方言說...
  • 縱 : Ⅰ動詞1 （釋放; 放走） release; set free; let go 2 （放任; 不約束） indulge; give oneself up to; l...
  • 子 : 子Ⅰ名詞1 （兒子） son 2 （人的通稱） person 3 （古代特指有學問的男人） ancient title of respect f...
  • 因 : Ⅰ動詞[書面語] （沿襲） follow; carry on Ⅱ介詞1 [書面語] （憑借; 根據） on the basis of; in accord...
  • 操縱 : 1. （控制; 開動） operate; control; roll; steer 2. （支配;控制） rig; manipulate; govern
  1. A group of related and closely linked structural genes, together with the operator gene that controls their expression are collectively called an operon.

    一組相關的、緊密連鎖的結構基因加上控制其表現的操縱基因，統稱操縱子。
  2. Then the engineered genes of bio operon were carried on testing of the functional expression, and biow & biob gene were induced to express

    而後對改造后的生物素操縱子基因進行了功能表達檢測及biow與biob基因的誘導表達。
  3. Operon is a unit of bacterial gene expression and regulation, including structural genes and cis - acting control elements in dna recognized by regulator gene product ( s )

    控制某一代謝途徑的相關基因，緊密連鎖地排列在一起，受同一操縱子控制。
  4. Like eukaryotes, but unlike bacteria, they have introns in their transfer rna, but like bacteria they have polycistronic operons ( gene regulators )

    像真核生物而不像細菌，轉運rna中含有內含子，還有細菌不具備的多順反子的操縱子（基因的調控子） 。
  5. 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。
  6. This experiment probed how to improve the expression efficiency of the structural genes of bio operon, and provided the feasibly researched route and scientifically theoretical foundation

    旨在探索如何提高生物素操縱子基因的表達效率，為該操縱子基因的高效表達提供可行的研究路線和理論依據。
  7. Used the genomic dna extracted by low melting - point agarose embedding method as pcr template, the full length of structural genes of bacillus subtilis bio operon were gained by long pcr method

    將該方法提取的基因組dna稀釋100倍作為模板，採用長距離pcr方法，獲得了枯草桿菌生物素操縱子基因全長。
  8. However, in the late phase of the growth, the strain hv grew a little faster than e. colihms174. hv ( ptz101 ) was constructed by the plasmid containing the phb operon and the parde gene tansformed into the strain hv

    將帶有phb操縱子和質粒穩定分配基因parde的質粒ptz101引入vhb整合菌中，構建成為產phb的vhb整合菌hv （ ptz101 ） 。
  9. J mol biol., 1992, 224 : 53 - 63. 26 abe h, aiba h. differential contributions of two elements of rho - independent terminator to transcription termination and mrna stabilization. biochimie, 1996, 78 : 1035 - 1042

    通過計算，我們預測到266個不依賴終止子，其中包括232個蛋白編碼基因， 12個trna基因和3個rrna基因，約17 %不依賴終止子位於操縱子的末端。
  10. Further analysis showed that there are regulatory elements, including tata box and caat box, etc. pc - igs fragments were cloned and sequenced from five strains of arthrospira ( a. platensis fachb341, a. platensis fachb439, a. platensis ouqds6, a. maxima ouqdsm and a. platensis fachb791 ) and two strains of spirulina ( s. subsalsa fachb351 and spirulina fachb440 ). the cloned fragment includes 494 bp of cpcb, 252 bp of cpcaand 111 bp of pc - igs sequence

    在節旋藻和螺旋藻分子系統學研究中，克隆了節旋藻和螺旋藻的藻藍蛋白操縱子中的pc - igs序列並進行序列測定和分子系統學分析，結果如下：所克隆的長度為857bp的片段包含有494bp的cpcb基因， 111bp的pc - igs序列和252bp的cpca基因。
  11. The c - phycocyanin ( cpc ) operon of blue - green alga ( or cyanobacteria ) arthrospira platensis fachb341 was cloned, sequenced and characterized by using chromoseme walking method. the sequence includes cpcb gene ( 519 bp ), cpca gene ( 489 bp ), cpch gene ( 357 bp ), and upstream sequence of cpcb ( 427 bp ) and upstream sequence of cpch genes ( 184 bp ), 111 bp of phycocyanin intergenetic spacer ( pc - igs ). upstream sequence of cpcb gene was ligated into promoter - probe vector pegfp - 1 and transformed into three systems : e. coli, synechocystis pcc 6803 and a. platensis fachb341 by supersonic and electrophoresis methods

    根據genbank中報道的節旋藻藻藍蛋白基因序列設計引物，首先克隆了鈍頂節旋藻（ arthrospiraplatensisfachb341 ）藻藍蛋白操縱子中亞基基因、亞基基因部分序列及二者之間的間隔區序列（ pc - igs ）並進行序列測定，然後根據此測序結果設計引物，通過染色體步移法克隆得到藻藍蛋白操縱子長度為2086bp的基因片段，其中包括藻藍蛋白亞基基因（ cpcb ， 519bp ） ，亞基基因（ cpca ， 489bp ） ，連接蛋白h基因（ cpch ， 357bp ） ，亞基基因上游啟動子序列（ 427bp ）以及各基因之間的間隔區（ pc - igs ， 111bp ； cpch與cpca間隔區， 184bp ） 。
  12. High stability of ptr102 - derived marking plasmids indicated that novel vector systems based on ptr102 could be constructed for the study on molecular biology and ecology of m. huakuii. 1kb gfp cdna fragment amplified by pcr was cloned into e. coli expression plasmid pet - hc, which was under the control of rna polymerase gene promoter from phage t7 with its own translation initiation codon

    將pcr擴增的1kbgfpcdna片段克隆到大腸桿菌表達載體pet - 11c上，使gfpcdna在帶有lac操縱基因的t7噬菌體rna聚合酶基因啟動子的控制下、以自身的atg作為翻譯起始密碼進行翻譯。
  13. Overall investigation of physiochemical features and biological factors of reservoir water quality were conducted in daoguanhe reservoir from 1999 to 2002. at the basis of these investigations, integrate evaluation of trophic state and environmental status was made. theoretical base for the reasonable utilization of fishery resource and ecological management of environment were provided using bio - manipulation technique and ecoenergetics means

    1999 ? ? 2002年全面調查了武漢道觀河水庫的水質理化特性和生物因子，在此基礎上綜合評價了水庫的營養狀態和環境現狀，並利用生物操縱技術和能量生態學手段，為水庫漁業資源的合理利用和漁業環境的生態學管理提供理論基礎。
  14. 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
  15. 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。
  16. Based on the analysis of the definition and the study of the estimation methods, the fighter ' s combat effectiveness model, in which the parameters of maneuver, cannon, missile, detector and others are considered, is established. the model has been tested with the existing aircrafts. it is shown that it is available and accurate enough for engineering practice

    在分析和研究作戰效能定義、作戰效能評估方法的基礎上，建立了能反映飛機機動性、火力、目標探測能力、電子戰能力、操縱效能、生存力、航程、突防能力、遠程武器能力、導航能力、載彈量等因素對飛機作戰效能影響的作戰效能計算模型。
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