密株 的英文怎麼說

中文拼音 [zhū]
密株 英文
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  • : Ⅰ名詞1 (秘密) secret 2 [紡織] (密度) density 3 (姓氏) a surname Ⅱ形容詞1 (距離近; 空隙小)...
  • : Ⅰ名詞1. (露在地面上樹木的根和莖) root and stem of a tree above the ground 2. (植株) individual plant; plant Ⅱ量詞(棵)
  1. The result showed that this strain have a strong ability to decompose the filter paper cellulose. in the process of degrading fibre, the strain adhere tightly to the fibre through its bacilliform cell

    結果表明該菌具有較強的分解纖維素的能力,菌在降解纖維素濾紙過程中與纖維素物質緊結合,同時菌體嵌入到濾紙纖維內部。
  2. Herbs bourgeoned with a high density and a low coverage in early july. with the coming of rain season, the velocity of growth in herbs enhanced with the higher coverage in august. in september, the growth of herbs stopped and the density and coverage of herbs descended

    草本植物在7月初萌發,平均度大,但植較小,蓋度也小;隨著降雨量的增加,在8月份一一草本植物的快速生長期,草本植個體長大,平均蓋度達最大值,但是度卻有所下降;到了9月中下旬基本成熟並逐漸死亡,蓋度和度均下降。
  3. Luyu 2, luyu 4, yedan 12 and yedan 13 all have a compacted plant shape with leaf upward and are all cold - resisting and suitable for close planting

    魯玉2號、魯玉4號、掖單12和掖單13都具有緊湊型,葉片直立、抗寒、適合高度種植。
  4. Among the 17 isolates, 8 isolates display tcg - ttg mutation in codon 531, 5 isolates have cac - tac or aac or cgc mutation in condon 526, 3 isolates have gac - gtc mutation in codon 516, and the last one has caa - aaa mutation in codon 513

    其中8為531位碼子tcg ttg的突變, 5為526位碼子cac tac或aac或cgc的突變, 3為516位碼子gac gtc的突變,另一發生了513位碼子caa aaa的突變。
  5. There are many adaptive changes in the two research subjects ( artemisia. songarica schrenk. and seriphidium. santolinum ( schrenk ) polijak. ) in morphology and anatomy, such as with the increase of the daily age, the root - shoots ratio increased ; the root became stronger ; the ratio of leaf volume and leaf area increased ; the volume of epidermic cell decreased ; the cut - icle and phellem layer on the surface of root thickened. stoma caved in leaf ; epidermal hair of leaf and stem well - developed, palisde tissue developed well, the cell gap decreased ; the spongy tissue disappeared ; leaf is kinds of isolateralthat is the typical xeromorphic structure ; crystal cell and fibric cell increased ; conducting tissue and mechanical tissue developed well ; bundle sheath appeared

    實驗研究的兩種菊科( compositae )植物(準噶爾沙蒿( artemisiasongaricaschrenk )和沙漠絹蒿( seriphidiumsantolinum ( schrenk ) poljak . ) ) ,形態解剖方面的變化表現為:隨日齡增加,根長/高比值日益增大;根系逐漸發達;體積與葉面積比逐漸增大;表皮細胞體積變小;角質層增厚;根外部出現加厚的木栓層;氣孔下陷;葉、莖部的表皮毛布,柵欄組織日益發達;而細胞間隙日漸變小;海綿組織逐漸消失;葉面結構常為典型旱生結構? ?等葉面;晶細胞及纖維細胞數目增多;輸導組織、機械組織日漸發達;具有維管束鞘等等。
  6. According to these problems, we adopt to the method of mending material, optimize to fermentation media and partly ferment condition. finally, we excogitate a kind of fermentation technology that is suitable for target gene efficiency expressed and is advantageous of product purified. with the plasmid pbv220 - ifnr, pbv220 - hgfa, pbv220 - hgfb, pbv220 - hpk5 that expresses serve as the model, adopting the biostat - c15l of b. braun company, utilize the method of mending material to ferment, through optimization fermentation media and optimization partly ferment condition ( ventilate quantity, stir speed, mend material speed ), eventually establishment a kind of fermentation technology that is suitable for target gene efficiency expressed and is advantageous of product purified

    以我室構建並穩定表達的重組質粒pbv220 - - ifn 、 pbv220 - hgf 、 pbv220 - hgf 、 pbv220 - hpk5為模型,分別從不同的表達宿主菌中篩選出一種適合大規模生產的菌種bl21 ( de3 ) ,該工程菌連續傳代100代表達質粒不丟失,表達量穩定;採用b . braun公司的biostat - c15l自控發酵罐,運用分批補料技術分別進行四種工程菌的高度發酵,通過優化工程菌發酵的培養基配方及優化部分發酵條件(通氣量、攪拌速度、補料速度) ,最終建立一種適于目的基因高效表達的高度發酵工藝模式。
  7. In this paper, first strand cdna of 3abc gene was synthesized using template rna extracted from cells infected with fmdv. the complete 3abc gene about isoobp was amplified by pcr and ligated into pgem - t easy vector. after transforming e. coli dh5 a, ampicillin resistant colonies were isolated and plasmid dna was prepared and analyzed by restriction analysis and pcr. presence of the full length 3abc gene was verified by nucleotide sequence analysis and the plasmid containing the expected sequence was named as pgem - 3abc. comparing the aquired sequence of 3abc with that of reference strains, the homology is more than 99 percent. the pgem - 3abc was digested with sal i and bgl ii and ligated into xho i and bgl ii - digested expression vector ptriex - 4 neo. lt was identified by restriction analysis and pcr and sequencing that this fragment had a 17bp deletion hi the nucleotide sequence 708bp of 3abc gene, which happened to form a terminator codon behind 3ab gene, but it contained the complete open reading frame ( orf ) of 3ab gene. positive clones were selected and induced with lmmol / l isopropyl - d - galactoside ( iptg ), bacteria were detected by sds - page and western blotting after properly treated. the results showed that the 3ab gene expressed successfully in e. coli and 33. 5ku fusion protein can be recognized by the positive bovine serum of fmdv. the amount of target protein is over 26 % of the total bacteria protein by gel thin layer scanning analysis

    擴增產物連接到pgem - teasy載體中,轉化大腸桿菌dh5菌,篩選氨芐青霉素抗性菌落,提取質粒經酶切鑒定、 pcr分析以及確證性測序證明,所克隆的1500bp左右的片段含有完整的3abc基因,與國外參考序列相比,同源性在99以上。將重組質粒pgem - 3abc和表達載體ptriex - 4neo分別用sal和bgl與xho和bgl消化后,亞克隆3abc基因至原核表達載體ptriex - 4neo中,通過酶切鑒定、 pcr擴增以及序列分析,發現克隆到ptriex - 4neo載體上的片段於3abc基因708bp處出現了17bp的缺失,碰巧在3ab基因后形成一終止碼子,但3ab基因的閱讀框架完整,選出含有3ab基因完整閱讀框架的陽性克隆,用iptg誘導表達,收集菌液進行sds - page電泳、 westernblotting分析,結果表明, 3ab基因在大腸桿菌中成功表達,其表達產物為分子量33 . 5ku的融合蛋白,並能被口蹄疫病毒陽性血清識別。經薄層掃描分析,表達量占總蛋白量的26以上。
  8. The optimum density is difficult to specify in terms of trees per acre.

    很難定論究竟每英畝多少樹為最適度。
  9. In two other outbuildings, police found a sophisticated and costly set - up for growing plants, which was supporting no less than 1, 534 cannabis plants

    在另外兩間附屬建物中,警方查獲精且昂貴的作物栽種棚架,用來支撐不少於1534的大麻作物。
  10. With extension of the stolon, changes of the internode length, branching intensity and ramet length were fit to exponential model. it seemed to " flexibly " adapting to the habitat because the clonal architecture of s. vulgaris had both the traits of " guerilla " and " phalanx "

    長度、間隔物長度和分枝強度隨匍匐莖延伸呈指數模型變化,其克隆構型兼有「游擊」型和「集」型的特點,能比較「靈活」的適應環境。
  11. Description : perennial herbs, 5 - 20 cm tall, densely white villose ; roots slender, terete, up to 40 cm long, fleshy, stem buried in sand with apical part emerged above ground

    形態特徵:多年生草本,高5 - 20厘米,全被白色長柔毛;根細長,圓柱形,長達40厘米,肉質;莖大部埋藏於沙中,部分露出地面。
  12. The deleted mutant pap gene was also cloned into yeast secreted expression ppic9k vector to form ppic9k ~ 3, then the vector was transferred into pachia pastoris gs115 strain. the specific expression protein was secreted into the medium after inducing with methanol and the protein amount reached about 50 - 60 u g per millilitre measured by uv - absorbed methods in the supernatant of the medium via high density fermentation. sds - page results showed that there was one protein band in the gel which molecular weight was about 34ku

    將缺失型pap基因克隆于酵母分泌型表達載體ppicgk構成重組載體,然後導入畢赤酵母( p8chianastoris )菌gslls細胞中,在甲醇的誘導下,經過酵母高度發酵進行pap的表達,經sds page分析,結果表明,在培養基上清液中含有一明顯的特異性蛋臼條帶,大小為34ku ,經western blotting分析,該蛋白與法國pap抗血清有特異性反應,體外活性檢測表明該蛋白對tmv的侵染性具有高度的抑制性,說明該pap基因在畢赤酵母gs中也得到了正確表達。
  13. The space distribution of pigment gland density on eleven places was analyzed by allotetraploid of ( g. arboreum g. bickii ) and varieties with pigment gland of g. hirsutum g. barbadense and the progeny population which is crossed by allotetraploid of ( g. arboreum g. bickii ) g. hirsutum and ( g. arboreum g. bickii ) g. barbadense

    摘要利用(亞洲棉比克氏棉)異源四倍體和陸地棉、海島棉有色素腺體品種以及由(亞洲棉比克氏棉)異源四倍體為母本,以陸地棉和海島棉有色素腺體品種為父本,組配成的雜交後代群體,對植上十一個部位色素腺體度在群體內的分佈進行了初步分析。
  14. The great bustard selects the areas with abundant plant species. higher vegetative cover score. smaller proportion of bare area and taller plants to display on postfire grasslands ; the important factors that influence the great bustard to selection display fields are the proportion of hay, stipa baicalensis density and the thickness of hay on unburing grassland

    在火燒地,大鴇會選擇植物種類數較多、蓋度較大、裸地比例較小及植相對較高處進行求偶炫耀;在非火燒地,枯草比例、貝加爾針茅度及枯草厚度是影響其求偶場選擇的重要因素。
  15. By the technology of gene cloning, bioconversion of d - amino acids with engineered cells containing d - hydantoinase and d - carbamoylase would be expected to overcome the drawbacks presented by using the original strains described above. according to the reported amino acid sequence of d - hydantoinases, two primers were designed and synthesized

    本文根據文獻報道的海因酶基因序列及大腸桿菌對碼子的偏愛性分別設計了正向及反向引物,以基因組dna為模板,利用pcr技術擴增得到菌pseudomonasputidayz - 26和sinorhizobiummorelensess - ori的d -海因酶基因。
  16. When plotted on a page the information looks like a giant, bushy tree, hence the project ' s nickname

    將這些信息繪制到紙上時,它看起來就象一巨大茂的樹,所以這項工程起名「生命之樹」 。
  17. Great diversity in genomic dna of gastrodia elata bl. and armillaria mellea. was also demonstrated by completely different bands of the rapd between various growing periods of t8 and m. the complete different bands of the rapd between m and the tuber of t8 might revealed that the genetic matter of m did not invade the inter area of gastrodia elata bl

    2通過對同一不同生長時期的天麻與蜜環菌的rapd擴增結果的研究表明:同一天麻不同生長時期的dna不表現差異,而且與環菌沒有共同的條帶,這說明環菌與天麻的dna有較大的差異,特別是與塊莖之間的差異說明環菌的遺傳物質在天麻的生長過程中侵入天麻塊莖皮層以內的部位時已被同化。
  18. By changsha, zhuzhou and xiangtan developing knowledge intensive industries or capital intensive industries mainly, the other regions developing labor intensive industries or natural resource intensive industries mainly, cultivate mul - layer industrial clusters system of our province. implement favourable policy and carry out institutional innovation so as to improve regional soft and hard settings. introduce managers hard, exalt entrepreneur ' s quality and construct an entrepreneur team who take on internationally strategic eye - sight

    實施產業集群發展戰略必須採取相應的政策和措施,比如區分產業集群和產業政策觀點,實施鼓勵集群發展的政策;以長潭地區發展知識或資金集型產業為主,其他市州縣發展勞動或資源集型產業為主,培育和發展我省多層次產業集群體系;實施優惠政策,進行制度創新,改善區域軟硬環境;積極引進人才,提升企業家素質,建設一支具有國際戰略眼光的企業家隊伍;塑造信任、合作、創新的區域和集群文化;加大專業市場建設力度,努力打造區域品牌,推進區域營銷等。
  19. Seiko precision ( hong kong ) ltd. was founded in may of 1997 as a subsidiary 100 % owned by seiko precision inc. in order to distribute clock movements for all markets except for japan

    精工精(香港)有限公司於1997年5月成立,是日本的精工精密株式會社,設于香港的全資附屬公司,主要職務是營銷石英鐘機芯,市場對象是日本以外的其他國家和地區。
  20. Over a century passed since seiko precision inc. japan, formerly named seikosha co., ltd, started manufacturing clocks in japan in 1892

    始創於1892年,日本的精工精密株式會社,前名為精工舍式會社,累積跨越一個世紀生產時鐘的經驗。
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