編碼段 的英文怎麼說

中文拼音 [biānmǎduàn]
編碼段 英文
coding section
  • 編 : Ⅰ動詞1 （編織） weave; plait; braid 2 （組織; 排列） make a list; arrange in a list; organize; gr...
  • 碼 : Ⅰ名詞（表示數目的符號或用具） a sign or object indicating number; code Ⅱ量詞1 （指一件事或一類的...
  • 段 : Ⅰ量詞（部分） section; segment; part; paragraph; passage Ⅱ名詞（姓氏） a surname
  • 編碼 : encoded; code; coded; encrypt; codogram; coding編碼表 encode table; 編碼程序 builder; 編碼尺 code...
  1. In the experiment, the full code sequence of bar gene was cloned by pcr from transgenic herbicide resistant bobwhite wheat and checked. it was expressed in e. coli and its protein was determined. after having been properly modified, the bar gene which correctly codes pat was cloned into binary vector pbi121 and then transferred into lba4404 by triparantal crossing, which is the prerequisite work for genetic transformation

    本實驗從抗除草劑轉基因bobwhite小麥中，利用pcr克隆的方法擴增出bar基因全長，並在原核表達系統中表達，鑒定表達蛋白的活性，將能夠正確編碼ppt乙酰轉移酶的bar基因片段，經過適當的修飾構建入真核表達載體。
  2. This dissertation brings forward and realizes the multilevel classifiable method which is based on characters coding. above all, this method realizes the first - grade classification by extracting enough effective characters from characters and coding them, to the others which coundn " t be recognized by the first - grade classification, the method will adopt the second - grade classification using template matching to recognize these characters

    本文提出並實現了基於特徵編碼的多級分類識別方法，通過給字元抽取足夠多的有效的特徵並給特徵編碼實現第一級分類，對于第一級分類后仍不能區分的字元，再進入第二級分類用模板匹配的方法最終達到區分的目的，這種方法的重點在第一級分類階段。
  3. 8 % ), which is similar to the mt protein of ostrea edulis while different from that of drosophila and mammalian ( no aromatic amino acid and histidine ). comparison of the deduced amino acid sequence of housefly mt with other species " mt showed that its identity with drosophila was highest, attain 65 % ; the different metallothioneins, within a part species of invertebrate, were 35 % - 41 % isologous ; its identi ty wi th the mt - ii of green monkey was 41 % and that with the human mt - ii was 35 %

    由擴增片段的編碼序列所推導的家蠅mt與其它生物mt比較顯示：家蠅mt氨基酸序列與果蠅（ drosophilamelanogaster ） mtn氨基酸序列的同源性最高，達到65 ；與部分無脊椎動物mt氨基酸序列的同源性在35 - 41的范圍內；與部分植物mt氨基酸序列的同源性比較結果為：同源性最高的為孢子植物墨角藻（ fucusvesiculosus ） （ 51 ） ，而最低的為種子植物鼠耳芥（ arabidopsisthalianal ） （ 35 ） ；與哺乳動物綠猴mt -的同源性達到41 ，與人類mt -的同源性為35 。
  4. The length of this phytase gene is1506bp interrupted once by an intron of 102bp in the 5 " part of the gene, this intron contains donor sequence - gtatgc, lariat sequence - gctgac and acceptor sequence - cag which are typically conserved sequence of the intron of fungal phytase gene. this gene encodes a peptide of 467amino acid residues with molecular weight of 51. 37kda, containing 13 potential n - glycosylation sites and a signal peptide sequence made up of 19 amino acid residues at n teminal of the peptide

    核苷酸序列分析表明， pcr擴增產物中包含有完整的phya基因，該基因全長1506bp ，其中包含一段長102bp的內含子，該內含子具有真菌植酸酶基因內含子的特徵保守序列： donor序列? gtatgc ， lariat序列? gctgac及acceptor序列? cag 。該基因編碼467個氨基酸，理論分子量為51 . 37kda ，其上有13個潛在的n -糖基化位點， n端19個氨基酸為信號肽序列，植酸酶活性位點序列（ crvtfaqvlsrhgaryptdskgk ）位於氨基酸序列的+ 71 + 93 。
  5. Two positive clones were sequenced, and the results showed that its nuclcotidc sequence includes an open reading segment which codes for a 45 - amino acids protein and three endonuclcase sites which arc1 bgii, bamh i and bgi ii, this protein was identified as metallothionein based on its characteristic described above and its similarity ( 85 % ) to the mtn gene of drosophila : the 10 cysteine residues present occur in five pairs of cys - x - cys, x is serine, valine, ilistidine or lysine

    結果顯示：擴增的cdna片段長度為289bp ，其中含有一個編碼45個氨基酸的開放閱讀框，閱讀框所編碼的氨基酸中含有10個半胱氨酸，且在序列中均排列成cys - x - cys ，其中x為ser 、 val 、 his或lys 。這些特徵說明擴增的基因片段為家蠅mt基因序列的一部分。此基因序列片段與果蠅mtn基因序列的同源性達到85 . 0 ，擴增的基因序列中含有三個內切酶位點bg 、 bam和bg ，這一點也和果蠅mtn基因十分相似。
  6. In this study, we at first aimed at obtaining the gene encoding the specific ige antibody related proteins by immunoscreening the schistosoma juponi cum adult worm cdna library with the pooled high - titer ige antisera from the individuals living in the schistosome epidemic regions

    J測定。 jnij序結果顯示，該插入片段為1200hp ，第一開讀框長507hp ，編碼169個氨基酸殘基，理論分子量為19 3kdi 。
  7. Rt - pcr was used to amplify the cdna of the genome. these cdna fragments were cloned into the plasmid pucm - t. the result indicated that the seguence of the genome was obtained. the genome of aev - nh937 composed of 7055 nucleotides, potentially encodes a polyprotein of 2134 amino acids. the genome of aev - nh937 has 94. 3 % nucleotides identity with the calnek vaccine strain of aev

    把它們分段克隆在pucm - t載體上，經序列分析，獲得了aev - nh937毒株的基因組全序列及推導的氨基酸序列，基因組全長為7055個核苷酸，與calnek疫苗株具有94 . 3的同源性，編碼一個含2134個氨基酸的多聚蛋白。
  8. This sequence emergences fourteen times from 1000 ests library indicts that it is a middle affluently gene in cdna library. the cdna of 634 basepairs contains an open reading frame of 339 nucleotides encoding a novel nonspecific lipid transfer protein. the first 23 amino acids constitute the putative signal peptide, characteristic for targeting to the secretory pathway

    測得th - nsltp序列全長為634bp ，含有一個非特異性脂轉移蛋白與植物耐逆性的相關性研究編碼112個氨基酸的閱讀框架， n端的23個氨基酸組成一段信號肽序列，表明它可能和分泌有關。
  9. The numerical simulation equations of the border curves in term of and as well as the matching rules and the frequency dependence of microwave electromagnetic parameters of a broad - band homogeneous absorbing coating with a finite value of reflection loss are available. these results pointed out the direction to develop rams ". according to the radar - absorbing model, the optimized design of rams with thin - layer, light - weight, broadband and strong - absorbing is available by the simple genetic algorithms, which can effectively conduct the research work of rams to the detail. small but completely, the electromagnetic parameter ' s databases of rams that based on actual microwave absorbers have been set up, the object function has been constructed which conform to the involved goals, the adaptive coding measure is taken which extends the coding length dynamically adapting to the condition of the number of actual absorbers or the precision of thickness and absorber - volume - percentage, the decoding technique is initiated which satisfies light - weight and strong - absorbing as well as thin - layer and broadband by adopting of tracing variable restricting conditions dynamically to control total thickness. when decoding, the variable restricting conditions of thickness are dynamically traced, so gain the radar absorbing coatings of light - weight multiple - layer single - ingredient. similary, of thickness and absorber - volume - percentage, of light - weight multiple - layer multiple - ingredient. also, the rams ' demand to radar - absorb performance as frequency is met making use of the penalty function

    作為遺傳演算法的具體實施：根據本實驗室近來研製的吸波材料，建立了吸波材料的相關數據庫；構造了能真實體現「薄、輕、寬、強」優化目標的目標函數；根據材料的實際數量以及塗層厚度精度要求、吸收劑體積分數精度要求，建立了能動態擴展相應碼長的自適應編碼方法；首創了通過動態跟蹤變量的約束條件來控制塗層總厚度的解碼技術，以此實現了在不弱化寬頻、高強的吸波性能目標的同時，兼顧到薄層、輕質的使用性能要求；在解碼時通過動態跟蹤厚度變量的約束條件，實現了多層單組分吸波塗層對重量輕的要求；通過動態跟蹤厚度變量的約束條件和吸收劑體積分數的約束條件，實現了多層多組分吸波塗層對重量輕的要求；使用權重系數變化法，實現了吸波塗層的分頻段吸波性能要求。
  10. To search proteins that associate with the mouse mint protein and regulate notch signaling in nuclei, and to study the function and mechanism of mint - mediated transcription repression, yeast two - hybrid assay was used to screen proteins that interact with a fragment of mint ( f5, amino acids 2226 - 2959 ). from 4x106 yeast clones transformed with the bait plasmid and a cdna library of 9 dpc mouse embryo, fifty - one were positive for nutritional screening and p - galactosidase assay. restriction digestion identified 10 independent positive clones and these were analyzed by dna sequencing these clones represent 3 correctly fused cdna fragments, which are mint, alpha a - crystallin - binding protein i ( alphaa - crybpl ), and nuclear receptor co - repressor 1 ( n - corl ), respectively

    鑒于mwt基因編碼區較長，共有10799個堿基，故此我們將mint分為六段，分別命名為fi一f6 ，本研究以其中的f5 （ 222e959 ）和f6 （ 296s576 ）片段為研究對象，將h者分別插入pgb盯7載體中，結果顯示： mintfs可與核受體輔助抑制因子1階cori ） ， o晶狀體蛋白結合蛋白1hlphatcrybp入及mw加互作用，而f6可與igm的重鏈恆定區、泛素結合酶2l6和一個未知功能的新的蛋白基因進行結合。
  11. Adopting the method of top - down, the virtual memory is divided into memory mange related unit ( segment unit and page unit ) and protection mode related unit ( protection test unit, debug test unit and exception detect unit ). data buses and control bused are designed separately for all of the units. vhdl codes are written and simulated

    Amex86的虛擬存儲器採用自頂向下的設計方法，把虛擬存儲器劃分為地址管理相關單元（又包括分段單元和分頁單元） 、保護模式相關單元（又包括保護測試單元、調試異常單元利異常檢測單元等） ，分別確立其數據通路和控制通路，完成了vhdl的編碼和模擬工作，通過測試程序模擬驗證了其功能的正確性並測定了基本性能。
  12. There are two obvious problems in the programming about embeded software of home appliances " controller. the first, there are lots of euseful code segments in the designed programs. the second, the technoligy ca n ' t succeed by reason of the dimission of software engineers

    在目前家電控制器嵌入式軟體的編碼過程中，存在兩個明顯的現象:一是軟體工程師編寫的程序代碼中有大量的可重用片段，二是軟體工程師的離職常常導致技術無法繼承。
  13. The cloning cdna fragment was extracted from positive clones and sequenced. the results showed that the cdna fragment was 816bp in size, encoding a protein which included 272 amino acids. the sequence homology analysis was carried out via the software blast 2. 0 network service in the four large databases - genbank, embl, ddbj, pdb, which had recorded 1 337 978 nucleotide and protein sequences. the results of the analysis indicated that the nucleotide homologous rates between the rubber tree etr and 15 recorded etrl of other plants ( mango, passion fruit, persia plum, strawberry, grape. . etc ) were 75 % - 80 % ; the protein homologous rates between the rubber tree etrl and these recorded etrl genes were 90 % - 95 %. from the results mentioned above, we could confirm that the cdna of rubber tree etrl had been cloned

    從陽性克隆子中提取克隆片段，經序列測定分析，結果表明，克隆片段的cdna大小為816bp ，編碼的蛋白質包含272個氨基酸。基因序列通過blast2 . 0networkservice軟體對genbank ， embl ， ddbj ， pdb四個大型數據庫中記錄的1337978條核酸和蛋白質序列進行序列相似性檢索，結果表明與芒果、一西番蓮、波斯梅、草毒、葡萄、西洋梨等15種已報道的植物的etrl基因cdnag的同源率為75 88 ；蛋白質氨基酸序列的同源率為90 95 ，表明本研究確實克隆到了橡膠樹etri基因的cdna序列。 4
  14. The start codon is at 84 - 86bp, the stop codon at 1658 - 1661bp. the homologous comparison of the deduced amino acid sequence with other plant epsp synthase proteins shows the identity to those of b. napus, a. thaliana, tomato, n. labacum respectively are 92 %, 91 %, 80 %, 65 %

    同源比較該段序列所編碼的氨基酸序列可以發現epsp合成酶有較高的保守性，它與歐洲油菜、擬南芥、西紅柿、煙草的同源性分別為920 、 91o 、 80o 、 65o 。
  15. In order to investigate the genomic organization of the single - nucleocapid nucleopolyhedrovirus of helicoverpa armigera, the ecori - n fragment located at 54. 8 - 59. 3 kbp of the viral genome was sequenced. the fragment contained 3762 bp helicase gene potentially encoding a protein with a molecular mass of 146 kda

    對棉鈴蟲單核衣殼核多角體病毒（ helicoverpaarmigerdsingle - nucleocapsidnucleopolyhedrovirus ， hasnpv ）基因組中ecori ? n片段進行序列分析，獲得了完整的解螺旋酶基因（ hel ） ，其開放閱讀框大小為3762bp ，編碼一個分子量為146kda的蛋白質。
  16. Besides, vgb gene expression also increased the chitinase secretion. in order to make the vitreoscilla hemoglobin gene express in bacillus subtilis, an inducible promoter ( levansucrase ) was cloned from b. subtilis wb600 and ligated with a promoter - less vgb gene. the resulted gene is called sacvgb and was demonstrated to express in e, coli by sds - page and carbon monoxide binding assay

    由於vgb基因啟動子不能在枯草桿菌中啟動表達，因此，根據已發表的果聚糖蔗糖酶基因（ sacb ）序列設計引物，從枯草桿菌wb600總dna中擴增出該基因的啟動子片段，然後將其與vgb基因編碼區及終止子序列相連，成功地組建了sacvgb融合基因。
  17. The 496 bp fragment of the orf of p22 gene and a 561 bp fragment were amplified from the genomic dna of zs strains of toxoplasma gondii. both 496 bp and 561 bp fragments were successfully cloned into the plasmid pthiohisa, b, c and pbudce 4. 1 respectively. 2

    從弓形蟲zs株基因組中擴增出p22編碼基因的一長496bp ，另一長561bp的片段，並成功構建含p22編碼基因的原核質粒重組體pthiohisa ， b ， c / p22 ，及真核重組表達質粒pbudce4 . 1 / p22 。
  18. The nucleotide ( nt ) sequence of the insert in phz1754 is 2299bps in size. computer assisted analysis of the sequence revealed an open reading frame ( orf ) with a g + c content of 70. 3 % that would encode a protein of 552 amino acids ( aa ). the nt seque nce comparision revealed that the orf in the sequenced region exhibits 85 % dna sequence homology with the cholesterol oxidase gene choa of streptomyces sp

    對phz1754進行外切核酸酶（ exonuclease ， exo ）順序缺失，獲得單向長度漸減重疊的系列突變體，核苷酸序列測定顯示出該ecor - sal片段的精確大小為2299bps ， frameplot程序分析揭示出該區域一個完整的開放閱讀框（ orf ）的存在，其大小為1656bps ， g + c含量為70 . 3 ，編碼552個氨基酸，利用blastsearch程序將orf的核苷酸序列及推導的氨基酸序列與因特網上基因及蛋白質數據庫進行綜合比較，發現無論在核苷酸水平還是在蛋白水平上，該orf均與膽固醇氧化酶表現出同源性，而且與鏈黴菌膽固醇氧化酶同源性最高，說明該orf編碼膽固醇氧化酶基因。
  19. The signature is a small piece of code, chosen carefully by the creator of the antivirus system that always appears in that virus but never in legitimate programs

    這個簽名是一小段編碼，是由總是出現在病毒中而在合法的程序里卻不會出現的反病毒系統的生成器仔細挑選的。
  20. There are no introns in all four genes and the length of the deduced mature bdnf ( 119 amino acid residues ) is the same

    但是這4種動物bdnf基因編碼區編碼的成熟肽段長度一致，分別為含119個氨基酸殘基的多肽。
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