結構基序 的英文怎麼說

中文拼音 [jiēgòujīxù]
結構基序 英文
structural motif
  • 結 : 結動詞（長出果實或種子） bear （fruit）; form （seed）
  • 構 : Ⅰ動詞1 （構造; 組合） construct; form; compose 2 （結成） fabricate; make up 3 （建造; 架屋） bui...
  • 結構 : 1 （各組成部分的搭配形式） structure; composition; construction; formation; constitution; fabric;...
  1. In this paper, a field strain of infectious bronchitis virus was isolated from proventriculus tissue, morphological observation by electron - microscope and the biological characterizations of the virus were studied, pairs of specific primers are designed and synthesized in correspondence with them, according to the published sequences of infectious bronchitis virus three structural protein ( spike protein s membrane protein m nucleocapsid protein n ) genes, the cdna of si gene, s2 gene, m gene. n gene of ib v isolate lx4 were amplified by rt - pcr and full sequences were first reported

    在此基礎上，根據國內外已發表的ibv基因序列，分別設計特異性引物，應用不同引物進行反轉錄合成cdna ，分片段對ibv的主要結構基因進行pcr擴增，並分別將各個目的片段克隆到puc19載體上，在大腸桿菌dh5中實現目的基因的分子克隆，經藍白斑篩選、限制性內切酶分析、 pcr鑒定，篩選出重組陽性質粒，並對各個目的基因片段進行序列測定，從而獲得ibv主要結構基因全序列。
  2. The ir sequence of mxmybl is most homologous with that of atmyb ( 86. 9 % ) and somewhat homologous with that of stmyb 1 ( 77. 0 % ) ; there is very low homology among n - and c - terminal regions outside of the ir regions of all of the mybs ; the protein mxmybl contains a proline - rich region as well as a serine - rich region near the c - terminus, such structure motifs are implicated in transcriptional activation

    9 ，與馬鈴薯stmyb的ir序列的同源性達77 0 ，所有這些nnrb蛋白除了瓜區具有較高的同源性外，其c端和n端幾乎沒有同源性。 mwyb蛋白的c一端還含有一個富含脯氨酸區，這樣的結構基序可能具有激活轉錄的功能。
  3. ( accession numbers : ay184425 - ay184440 ). combined with other several full 12s rrna sequences of chinese water deer, montijac, water deer, cow, horse, goat and tragulus retrieved from genbank database, the whole set of sequences was utilized for downstream analysis based on theories and models in molecular phylogeny, whereas the secondary structure of 12s rrna was predicted and analyzed based on present small subunit of ribosome model

    將上述序列與從genbank檢索到的獐、麂、水鹿、牛、馬、羊、鼷鹿的12srrna基因全序列一起，通過應用分子系統學理論與模型分析序列數據，以及對12srrna二級結構的分析，得出了以下主要結論： （ 1 ）用最小進化方法（ me ）和鄰接法（ nj ）對12srrna基因的全序列構建分子系統樹的拓撲結構基本相同。
  4. In addition, the well retained stability and integrity of cell membrane of boea leaves might also be an important mechanism which make them resurrect well. by using mrna differential display, 5 desiccation sensitive cdnas, 52 desiccation - induced cdnas, 21 up - regulated cdnas, 14 down - regulated cdnas and 16 phosphate induced cdnas were obtained. the cloning, sequencing, homological blasting and northern blotting results of 5 desiccation - induced cdnas and 3 phosphate induced cdnas implied that signal transduction induced by desiccation, regulatory gene cascades and functional genes such as g protein, protein kinase, vp3 - and mad3 - like genes might be involved in dehydration in the resurrection plant boea hygrometrica

    對其中5個脫水特異誘導表達牛耳草光合作廠j的脫水保護和復甦機理的cdna （包括可能與復甦能力有關的cdna ）和3個磷酸鹽處理誘導表達的cdna進行克險測序、同源性探測和northern雜交檢測表明，牛耳草脫水過程中誘導表達的基因可能涉及到脫水脅迫的信號轉導「蛋白、蛋白激酶等） 、調節基因的級聯作用（ vp3 ， mad3樣基因等） 、結構基因產物調節細胞結構（包括細胞質膜）在脫水脅迫中的穩定性等。
  5. Two strains of prrsv were isolated from the swine infected with prrsv in shangdong province and daqing area, in order to clarify the source and genetic background of porcine reproductive and respiratory syndrome virus ( prrsv ) from different parts of china, thus providing theoretic basis for the study of vaccine against it. the prrsv was cultured on mark - 145 cells for 5 ~ ~ 6 passages. when the cpe was obvious, the virus was harvested and purified

    為了弄清我國不同地區prrsv的來源以及其遺傳學背景，為疫苗學研究提供理論根據，本研究在ch - 1a株完整的基因組獲得以後，從流行於我國山東（ sd ）和黑龍江大慶（ dq ）地區疑似prrs的豬體內分離到prrsv ，在mark - 145細胞上盲傳5 6代，細胞出現明顯病變以後，收獲病毒液，然後提純，提取全病毒rna ，經過反轉錄、 pcr擴增獲得結構基因orf2 7的目的基因片斷，然後與pmd - t載體連接，轉化，得到陽性質粒后進行測序，並將其與ch - 1a株進行了比較分析，同時對這兩個毒株的結構基因組的理化性質進行分析。
  6. It discusses the characteristic of each level in osi model from the point of wwan first, then analyses clearly the primary technologies used in gprs / sms / csd and a topology structure model of the wwan based on gprs / sms / csd is presented. it also deeply discusses the integrate technology of gprs / sms / csd in a example of fujian environmental automatization system, at the same time a network model of wwan based on gprs / sms / csd is brought forward. last, there are the module programmers of the system

    本文從計算機開放系統互聯參考模型入手，按osi參考模型7層協議結構順序，逐步介紹了在無線廣域網環境中osi層次模型的特點，在此基礎上，詳細分析了gprs / gsm技術和簡訊息技術，並給出一個基於gprs /簡訊息/ csd的無線廣域網的網路拓撲結構；以福建省環境自動監測監控系統的分析和設計為例，探討了現階段gprs技術和簡訊息技術、電路交換技術在無線計算機網路系統中的集成問題，並給出了一個基於gprs /簡訊息/ csd的無線廣域網網路模型，最後是系統的模塊程序設計。
  7. During the work period in the southern zone of the east qinling belt, the process of sedimentation, basin quality and its interior structure and configure, important events are studied from the sinian to the triassic, especially through more than one hundred km profile across the southern zone of the east qinling belt. in the technical method, the basin dynamic analysis in the cambrian and the devonian respectively and the cycle events in the late triassic are added to the research of the belt. the some basic and important viewpoints of the orogenic - sedimentology are prompted in the study method, thought and connotation fields in this stage

    在東秦嶺南帶沉積盆地演化研究中：通過對東秦嶺南帶從震旦繫到三疊系的沉積作用過程，沉積環境展布和變化，沉積盆地性質、內部結構、層序、配置和發展演化，沉積過程中重大地質事件研究；隨著全球沉積地質計劃在全球的推廣和展開，在研究內容和技術方法上，增加秦嶺造山帶層序地層學以及沉積盆地動力學探索等沉積地質學前緣學科的研究，這樣從更深入和更廣闊的角度進行了這個造山帶的沉積盆地分析，在研究方法、思路和內涵上開拓了造山帶沉積學的一些基本觀點。
  8. Bioinformatic analysis were performed to prepro - gynostemminl on the base composition, codon preference, amino acid composition, pi value, molecular weight, secondary structure, prosite scan, prediction of protein localization sites. blast thtf arabidopsis thaliana genome, and 3d structure modeling

    運用生物信息學軟體對絞股藍班p前體進行堿基組成和密碼子偏倚性、氨基酸組成特徵、功能位點、亞細胞定位、跨膜結構、核酸結合基序以及空間結構等方面的分析。
  9. The full coding regions of bdnf genes were amplified from the genome of tylototriton taliangensis, phrynocephalus hongyuanensis, japalura splendida and cyclophiops major, respectively by pcr with the primers designed on the sequence of human bdnf gene. the pcr products were cloned into the vector pucis of esherichia coli. sequence analysis showed that the coding regions of three reptiles are the same ( 741 bp ) in length and these bdnf genes encode a peptide of 246 amino acid residues while that of tylototriton taliangensis is 744 bp in length and encodes a peptide of 247 amino acid residues

    根據已有的人bdnf結構基因的全長序列設計了一對引物，利用pcr技術分別從大涼疣螈（ tylototritontaliangensis ） 、紅原沙蜥（ phrynocephalushongyuanensis ） 、麗紋龍蜥（ japalurasplendida ）和翠青蛇（ cyclophiopsmajor ）的基因組dna中擴增到目的dna片段，並將其分別克隆到大腸桿菌載體中，然後對所獲得的陽性克隆進行測序。
  10. A new e. coli promoter - probe vector phn1005 was constructed by using a red - shift enhanced gfpmut3 as reporter gene and showed the following characters : 1, bamhi at the 5 " end of gfpmut3 structure gene could be used to clone promoter - active fragment and the strength of promoter could be quantitatively assayed. 2, a rrnbtlt2 terminator from rrna gene at the 3 " end of gfpmut3 could permit clone strong promoter. 3, another rrnbt1t2 terminator was inserted upstream bamhi to prevent reading through of promoters from puc19

    進一步以紅移且熒光強度提高21倍的gfpmut3為報告基因，構建了大腸桿菌啟動子探針載體phn1005 ，該載體上gfpmut3結構基因5 』端的bamhi位點可用來克隆具有啟動子活性的dna片段並定量分析插入的啟動子強度；其3 』端含rrnat1t2終止子，可允許克隆強啟動子；在bamhi上游同樣插入rrnat1t2終止子以防止載體puc19上的啟動子的轉錄通讀； gfpmut3結構基因上游還插入一段內含子序列使正反六種讀碼框的翻譯均可被終止，可保證gfpmut3以正確的讀碼框翻譯。
  11. Blastn analysis showed that each of the 10 sequences had no homology with the structural genes or regulatory genes in the anthocyanin biosynthesis. it was suggested that there were some limitations to isolate the specific ast gene by ddrt - pcr

    Blastn分析表明，這10個差異表達的cdna片段與數據庫中花青苷生物合成途徑中的結構基因和調節基因序列沒有同源性，表明用ddrt - pcr的方法克隆特定的ast基因有一定的局限性。
  12. In structural genomics, genetic maps have been constructed for up to 40 forest tree species, more than 30 commercially important qtls have been detected, comparative mapping has been done for a few of forest tree taxa, and whole genome sequencing was completed for populus and is under way for eucalyptus

    結構基因組學方面，已構建了近40個主要造林樹種的遺傳連鎖圖譜，在不同樹種中定位了30餘個重要的數量性狀位點，在部分樹種中開展了基因組比較和綜合圖譜構建研究，楊樹的全基因組測序已經完成，桉樹的全基因組測序正在進行。
  13. Now, the structure gene sequence and 3 ' - end gene sequence have been logged on genbank. the accession number is ay044918

    目前，此過敏蛋白tb22kda的結構基因與3 』端基因序列已在genbank登錄，登錄號為ay044918 。
  14. A pair of primer designed according to multi - sequence comparing results of published ibv sequences in genbank was used to amplify the nucleocapsid gene of 5 strains, the amplified rt - pcr product of all 5 strains is 1. 2kb in length

    對3個克隆質粒中的目的基因片段進行序列測定，結果表明該片段含有ibvn基因全序列，其結構基因全長1227bp ，編碼409個氨基酸。
  15. Because of the regular structure of web requests, basic url analysis is available for any web application

    由於web請求的常規結構，基本的url分析可用於任何web應用程序。
  16. Aiming at realizing an all - digital programmable qpsk modulator with data rates covering 2k ~ 2. 048mbps, this thesis puts research on modulator architecture, base - band signal shaping, programmable interpolation algorithm, and digital signal processing algorithms with fpga. we have completed the program design and the timing simulation, the pcb board has been fabricated. the similation result is given to verify the design

    本文以實現2k ~ 2 . 048mbps傳輸速率的變碼速率全數字qpsk調制器為目標，對全數字調制器結構、基帶成形濾波、高倍可變內插以及基於fpga的信號處理演算法等問題進行了研究，編寫了調制模塊的vhdl程序，完成了軟體環境下的驗證調試，並設計實現了板級調試系統。
  17. According to the amino acid sequence resulted from our previous research about tb22kda protein and the related literatures about gene sequence of allergenic protein in common buckwheat, we designed primers and got the structure gene successfully. by 3 ' - race method combined with nested pcr, the 3 ' - end nuclear acid sequence was also obtained ; in additon, for the 5 ' - end sequence, we selected a specific conserved nuclear acid sequence as the 5 ' primer and part of structure gene sequence as the 3 " primer, and till now, partial 5 ' - end sequence has been amplified as well

    本研究根據先前分離純化所得天然tb22kda蛋白經maldi - tof - ms （質譜法）測得的氨基酸序列和文獻報道的過敏蛋白核苷酸序列設計引物，擴增克隆了該過敏蛋白結構基因的編碼序列；根據測得的序列設計特異性引物，並利用3 』 - race方法結合巢式pcr擴增得到基因的3 』末端；依據同源性比較的結果選用一段保守序列為5 』引物，並根據結構基因內部序列設計3 』特異性引物，進一步獲得了該基因5 』端的部分序列。
  18. On the base of current spatial data structure, management technology of gis is discussed in the second chapter. using serialized file organizes graph data, and using relation database manage property data and linking data of graph and property data

    第二章在現有gis空間數據組織及空間數據結構基礎上，探討了gis數據管理方法；即圖形數據由序列化的文件管理，屬性數據及圖形和屬性數據的連接數據採用關系數據庫管理。
  19. Based on g - w contact model, two rough surfaces in contact were simplified to a smooth one and a rough one which has regular rectangular asperities, and a three - dimensional transient thermal and stress coupled fem model was established using thermal - structure sequential coupling. the course of the sliding with friction was simulated using the nonlinear multiphysics field fem, meanwhile considering thermal - elastic problems of the two bodies, to calculate and analyze the temperature, contact pressure and stress of the sliding contact surfaces with frictional heating

    基於g - w接觸模型，將兩個粗糙表面簡化為一個有規則排列的長方體微凸體的粗糙表面與一光滑表面，利用熱結構順序耦合建立三維瞬態有限元計算模型，考慮兩個物體摩擦接觸的熱彈性問題，採用非線性有限元多物理場來實現，對粗糙表面接觸模型的瞬時摩擦溫度場、壓力場和應力場進行了計算分析。
  20. This dissertation grounds on the development of pattern i / o module, some key techniques including the design of a register _ based interface circuit and the data generating and sampling circuit are discussed explicitly. on the basis of virtual instrument software architecture, the programme of the instrument driver and application software are discussed detailedly. and some idea and experience developed by the author in the course of debugging and testing the circuit are discussed also

    本文立足於vxi總線自動測試系統圖形i / o模塊的研製工作，在vxi總線系統體系結構基礎上，介紹了vxi總線圖形i / o模塊介面電路和數據輸入輸出功能電路的實現方案;在虛擬儀器軟體構架visa的基礎上，根據測試任務完成了vxi總線圖形i / o模塊儀器驅動器和應用軟體的設計與編寫;對驅動程序調試過程中出現的問題，進行了較深入的分析，並提出了實際的解決措施。
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