載綠體 的英文怎麼說

中文拼音 [zǎilǚtǐ]
載綠體 英文
chlorophore
  • 載 : 載Ⅰ名詞（年） year : 一年半載 six to twelve months; six months to a year; 三年五載 three to five ...
  • 綠 : 綠形容詞（像草和樹葉茂盛時的顏色） green
  • 體 : 體構詞成分。
  1. First, to construct a recombinant plasmid pegfp - c - fos with c - fos promoter and egfp, and then transfect it into human bladder transitional cell carcinoma biu - 87 cell ; second, based on the changes of the expression of gfp in the biu - 87 cell which induced by the aconitine and hab toxins, the concentration of the hab toxins could be detected

    目的：構建一個含c - fos啟動子和egfp報告基因的pegfp - c - fos重組質粒載體。體外轉染膀胱癌biu - 87細胞后，利用赤潮毒素作用后細胞表達綠色熒光蛋白的變化來檢測赤潮毒素，初步建立一種以細胞為基礎受體水平的赤潮毒素檢測方法。
  2. To investigate the consequence of this interaction, aes - rfp fusion protein expression vector was constructed and co - transfected into nih 3t3 cells with tle1 - gfp fusion protein expression vector. confocal microscopy observation showed that aes could interact with tle1 at the cytomembrane region. moreover, this interaction inhibited the concentration of tle1 into nucleus

    在構建了紅色熒光蛋白aes表達載體后，將其與tle綠色熒尤蛋白載體共轉染細胞，共聚焦顯微鏡觀察發現這兩種分子在胞漿中有共存現象，而且aes的表達可抑制tlei向胞核內的聚積。
  3. Third : carve out channel, using extracurricular action to solve environmental problem, chemistry extracurricular action is use environmental chemistry and green action a main carrier, the goal is improve students environmental consciousness, establish right environmental valuable, concept and attitude, consolidate students habits of environmental action, foster students craftsmanship which is how to solve environmental problem, and the trait is fit for environmental trait and need of the epoch development, bring into play students initiation plenitude, enhance students " entirety of diathesis, the students none but go deep into the society practice, join many kinds of exercise actively, they can get clear experience, realize the importance of the protect environment, on the other hand, they can study the knowledge about environmental chemistry, develop craftsmanship about protect environment, improve the students " ability of using the knowledge to solve actual environmental problem

    三、拓寬渠道，利用課外活動參與解決環境問題。化學課外活動是以環境化學和綠色行動為主要載體，以充分提高學生的環境意識、樹立正確的環境價值觀與態度、強化學生的環境行為習慣、培養學生參與解決環境問題的技能為目標，以最新的現代環境知識、環境觀念和學生的直接經驗為主要內容，以適應當地環境特點和時代發展需要，充分發揮學生的主體性、發展學生的全面整體素質。學生只有深入社會實踐，積極參加各種活動課，在活動中一方面獲得真切的感受，體會到環境保護的重要性，另一方面可使學生較好掌握環境化學有關知識，發展環保技能，提高學生靈活運用知識初步解決實際環境問題的能力。
  4. Green fluorescent protein ( gfp ) gene was conjugated to the 3 " end of the pap gene in order to screen easily of the transgenic cotton plants. the combined gene was cloned into plant expression vector pbi121 and then transformed. about 5000 seeds of the transgenic cotton were obtained and the some seedlings of the transgenic cotton could give a bright green fluorescence in the dark condition when the cotton seedlings were irradiated with ultraviolet rays

    為了便於轉基因棉花後代的篩選，在pap基因的3 』端融入了綠色熒光蛋白gfp ）基因，然後將融合基因克隆在植物表達載體pbi121上，再進行遺傳轉化，得轉基因棉花種子5000餘粒，將種子播種長到于葉展開時，先在黑暗中用紫外燈照射，查找表現綠色熒光的幼苗，然後再用地高辛（ dig ）標記的pap基因特異性探針對這些棉花進行點雜交，最後發現有8株棉花表現陽性反應，說明pap基因的確己經轉到了棉花的基因組中，其棉花黃萎病的抗性鑒定正在進行之中。
  5. It was confirmed by restriction enzyme digestion analysis that egfp fusion expression plasmids of scfvs were successfully constructed

    的序列正確，經酶切鑒定證實成功地構建了綠色熒光蛋白基因融合表達載體。
  6. Construction of recombinant adeno - associated virus vector expressing glial cell line - derived neurotrophic factor labeled by green fluorescent protein

    綠色熒光蛋白標記的大鼠膠質細胞源性神經營養因子重組腺病毒載體的構建及其表達
  7. The synthetic circuit is also simulated about normal working, green mode working and so on ; the results of simulation meet the function requirement

    在整體電路模擬中對正常工作、輕負載綠色模式過程等進行了驗證與分析，模擬結果表明該集成電路滿足設計要求。
  8. Three chloroplast transformation vectors including pds16s - cat, ptn1269 - bar and psp72 - n5 - bar - n3 were constructed, using ! 6s rrna or chln gene sequence as a homologous segment and cat or bar as a selective marker gene, respectively. foreign genes were introduced to the cells of d. salina by microprojectile bombardment method and a pilot chloroplast tran

    3 .杜氏鹽藻葉綠體165出na基因的克隆和轉化載體的構建根據杜氏鹽藻的近緣藻類的葉綠體基因組序列資料，克隆了杜氏鹽藻葉綠體16srrna基因部分序列1100bp ，並利用克隆的16srrna鄭州大學2003年博士學位論文
  9. Finally, the author puts forward the countermeasures and the suggestions in the development of the animal husbandry in jiuquan oasis, which are to confirm the rational amount of domestic animal loaded ; to protect the meadow resource and to develop the high - quality artificial meadow energeti cally ; to implement the virtual water strategy in order to alleviate the ecological environment pressure in jiuquan oasis ; to advance the industrialization process of animal husbandry energetically ; to process and utilize crops by product in the agricultural district ; to strengthen the construction of shelter forest of qilian mountains ; to organize the seasonal production of the animal husbandry ; to popularize the fatten poultries technology in the other land ; to strengthen the rational planning of the production of the animal husbandry ; to increase fund input ; to accelerate the basic construction of the animal husbandry and to prevent and cure the grassland which mouse hurt

    採用層次分析法對酒泉綠洲畜牧業發展的重要影響因素做了判斷。最後從確定合理的載畜量，大力保護草地資源和發展優質人工草地，實施虛擬水戰略以緩解酒泉綠洲的生態環境壓力，大力推進畜牧業產業化進程，對農區農作物副產品的加工利用、加強祁連山防護林建設、組織畜牧業季節性生產，推廣推廣肉禽異地育肥技術、加強畜牧業生產的合理規劃、增加資金投入，加快畜牧業基礎設施的建設以及草原鼠害的防治等十個方面提出了酒泉綠洲畜牧業發展的具體對策建議，以期望能對酒泉市的社會經濟發展提供科學的決策依據。
  10. In the third part of the thesis, a chlamydomonas reinhardtii chloroplast expression vector, pactbvpl, containing the fusion of the foot and mouth disease virus ( fmdv ) vp1 gene and the cholera toxin b subunit ( ctb ) gene was constructed. transformation of c. reinhardtii chloroplast was achieved by biolistic bombardment with pactbvpl

    論文第三部分主要敘述了將o型fmdvvp1與強黏膜免疫佐劑霍亂毒素b亞基（ ctb ）的融合基因克隆重組到衣藻葉綠體表達載體中，並採用基因槍法轉化衣藻葉綠體，獲得了具有壯觀黴素抗性的轉化子。
  11. But through masters love and blessings, and keeping her principle of positive thinking in mind, they decided to go ahead with the project anyway, saying, well, well just do it and pray to master for help. so they traveled to qualcomm stadium, wearing yellow and green vests bearing the words the san diego rescue team of the supreme master ching hai international association, and were ushered through several checkpoints by other rescue workers and the centers security guards

    盡管我們后來得知疏散中心不接受食物捐贈，但是在師父的愛力加持下，我們提醒自己要保持肯定的想法，因此下定決心，無論如何都要按計畫行事。同修穿上印有清海無上師世界會聖地牙哥救難隊字樣的黃綠色背心，來到qualcomm體育場時，我們順利通過了各檢查崗哨，並且受到疏散中心救災人員與警衛的歡迎，他們告知我們卸放食物的地方，然後開車載我們去拜會美國紅十字會的代表。
  12. The chloroplast shsp gene was screened from the cdna library of tomato flower by pcr strategy and confirmed by sequencing. but difference was found at 3 bases of the sequence from the reported in genbank. then, an integrated vector prok ii of the chloroplast shsp gene and nptii gene ( a kanamycin resistant gene ) with camv35s promoter was constructed and introduced into tomato mediated by agrobacterium tumefaciens lba4404. transgenic tomato were screened by their ability of growing on media containing kanamycin

    本實驗採用pcr方法從番茄花cdna文庫中克隆到葉綠體shsp基因，經測序證實與genbank中已發表的序列在編碼區相差2個堿基，其中一個堿基導致1個氨基酸的改變。將葉綠體shsp基因定向克隆于帶有組成性表達啟動子camv35s的植物表達載體prok中，凍融法轉化農桿菌lba4404 ，利用葉圓盤法對番茄進行ti質粒介導的遺傳轉化。
  13. In the research of transgenic fish, green fluorescent protein gene was sub - cloned to downstream of carp p - actin gene promoter that was cloned in pucusa by molecular recombination technology. thus pagfp plasmid was constructed successfully. the recombination was determined by digestion of restriction enzyme and sequencing

    實驗通過分子重組技術，採用定向克隆法將綠色熒光蛋白基因亞克隆到puc118a上鯉魚-肌動蛋白基因啟動子下游，構建成能在真核生物體內表達的表達載體pagfp ，經雙酶酶切法序列鑒定后，回收帶啟動子和目的基因片段。
  14. The gpa1 gene was obtained via pcr amplification and was cloned in the two - hybrid dna binding domain vector pgbkt7 the combinant plasmid was designated as pgbkt7 - ga. - galactosidase assay indicated that got did not have the property of self - activation. after pgbkt7 - ga was transformed to yeast pj69 - 4a, we transformed arabidopsis vegetative tissue two - hybrid cdna library plasmids to yeast pj69 - 4a containing pgbkt7 - ga

    通過pcr擴增得到gpa1基因並將其克隆到雙雜交dna結合域載體pgbkt7中，得到的重組質粒命名為pgbkt7 - g ， ?半乳糖苷酶活性鑒定表明g不具有自激活特性，將其轉化到酵母菌pj69 - 4a中，再以此為受體菌轉化擬南芥綠色營養組織cdna文庫質粒。
  15. Therefore, we will now regularly use the plugin tied up and made a component installation kits, this installation of the convenient things can be watching all the programs, it could also facilitate the unloading

    所以我們現在將經常使用的一些插件捆綁起來，做了一個控制項安裝包，這樣安裝了這個東西就可以方便的收看全部節目了，由於是綠色的軟體，同時也可以方便的卸載。
  16. She can you browse the internet in search of information they can be safe, nor download software to worry about, no software is bundled with the software capital of the green, she can a bundled software when installing the software separated into green, not authorized to stop bundling plug - in installation, and installation of all surveillance your system of documents, you can facilitate its arbitrary deletion

    她能使你在上網瀏覽、搜索資料時得以安然無恙，在下載軟體時亦無后顧之憂，也不再有捆綁軟體與綠色軟體之分，她能將一個捆綁軟體在安裝時分離成綠色軟體，阻止未被授權的捆綁插件安裝，並監視所有安裝到你系統中的文件，便於你能對其進行任意刪除。
  17. So, the green universities are important basement for improving environment quality of all society in a long run. this thesis focuses on background & basic information of environment management system and its auditing for the green universities

    建立綠色大學，不僅是環境教育的一種有效方式，而且是實施素質教育的重要載體，為提高學生綜合素質開辟一條新的途徑，從而對實現社會和環境的可持續發展產生持久而長遠的影響。
  18. In order to form a chloroplast transformation system of d. salina, we have conducted some studies including its sensitivity to antibiotics, the activity of promoter, cloning of the chloroplast genes and construction of transformation vectors, so far a pilot transformation system of the d. salina chloroplast has been completed. methods : the sensitivity of d. salina to seven antibiotics or herbicide used commonly in gene engineering was studied and the biological activity of atpa promoter from c. reinhardtii chloroplast was tested by using enhanced green fluorescent protein ( egfp ) as a reporter. primers were designed in the conservative encoding regions according to the chloroplast genomes from four algae which have close genetic relationship with d. salina, and the sequences of 16s rrna, chll and chln of d. salina chloroplast were cloned and sequenced, respectively

    方法:根據杜氏鹽藻的近緣藻類的葉綠體基因組序列資料，在基因編碼區的高度保守區域設計引物，克隆了杜氏鹽藻葉綠體165識na基因、咖l基因和ch n基因，並分別以165識na基因和chln基因序列為同源片段，以cat和bar基因為篩選標記基因構建了三套杜氏鹽藻葉綠體轉化載體: 2鄭州大學2003年博士學位論文杜氏鹽藻（ d ~ iiellasalina ）葉綠體轉化研究pds165一eaf 、 ptn1269一bar和psp72一5一bar一3 ，用基因槍法轉化杜氏鹽藻，初步建立起杜氏鹽藻葉綠體轉化體系。
  19. In the second part of the thesis, we described that a tobacco chloroplast expression vector, ptrvp1, containing the foot and mouth disease virus ( fmdv ) vp1 gene and the selective marker aada gene was constructed and transfered to the tobacci chloroplast genome by the biolistic method

    論文第二部分主要敘述了煙草葉綠體表達載體ptrvp1的構建，並通過基因槍方法轉化煙草葉綠體基因組，獲得了3株具有壯觀黴素抗性的轉化再生植株。
  20. To investigate whether it is suitable for biodegradable plastic production, we constructed the chloroplast integration and expression vector ptrv - phb, and integrated all the genes necessary for phb synthesis into tobacco chloroplast genome through gene - gun transformation. the chloroplast transformants showed phenotypically normal growth and were fertile

    本研究在國內率先探討將葉綠體轉化技術引入植物生產生物可降解塑料這一領域的可行性（國外僅有日本一例） ，構建了葉綠體轉化及表達載體ptrv - phb ，通過基因槍法將phb合成相關基因導入煙草葉綠體基因組。
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