indicated strain 中文意思是什麼

indicated strain 解釋
指示應變
  • indicated : 表計的
  • strain : vt 1 用力拉，拉緊，抽緊，扯緊。2 使緊張；盡量使用（肌肉等）。3 強迫，強制；濫用，盡量利用。4 拉傷...
  1. The blastn results show that gyn - 15 is closely related to a symbiont of anemones, s. californium, and the free - living strain, gymnodinium varians. sequence comparison show that the similarities among each part of the sequences from these three strains are all above 99 %. phylogenetic reconstruction with neighbor - joining ( nj ) method using sequences of variable regions ( v1 + v2 + v3 ) of ssu rdna indicated that gyn - 15, s. californium and g. varians form a new clade with 100 % bootstrap support

    以ssurdna序列中的三個可變區（ vz + vz + v3 ）和鄰接法困eighbor一joiningmethod ， nj法）構建共生甲藻屬的系統進化樹表明， gyn一巧與5 . cal扣rnium和g . varian :在共生甲藻屬內構成一個獨立的、自檢支持百分率為100 %的子類群（ clade ） ，根據這些結果可將gyn一巧初步鑒定為屬于共生甲藻屬。
  2. 5. exploring fermentation synthesis of quinic acid ( qa ) using bioengineering strain under shake flask conditions synthesis of qa using recombinant e. coli constructs was examined in m9 accumulation medium. the result indicated that qa was produced from d - glucose in the culture supernatant, but it is necessary to explore further the consequences of fermentation in next work

    工程菌搖瓶發酵產酸初步觀察初步探索了奎尼酸工程菌在m9積累培養基中的發酵產酸條件，結果表明工程菌經直接發酵由葡萄糖產生了奎尼酸，但尚須進一步優化發酵條件提高產酸率。
  3. The microbial agent ' s ability in straw degradation was detected by potted experiment and scanning electron microscope. the result indicated that after 15d the structure of straw was destroyed and did not float longer, which did not affect crop ' s rootage ; furthermore the effect on the next crop ' s growth was studied, and the results shown that the microbial agent could accelerate the next crop ' s growth. the strain b3 secreted incretion iaa and aba by tlc and immunological analysis

    通過盆栽試驗和掃描電鏡觀察檢測了秸稈降解劑對秸稈的降解效果，結果發現，該降解劑在15d內就能破壞秸稈的結構，使秸稈不再漂浮，不影響作物的生根；進一步檢測其對后季作物生長的影響發現，該降解劑還能促進后季作物的生長，薄板層析和免疫學檢測均顯示菌株b3分泌了iaa和aba 。
  4. Abstract : the therortical calculation of the bending stress of the root and experimental stress analysis on the modified profile and the standard involute tooth profile were made with the finite element method and the electric resistance strain film method. this indicated that the modified profile was supe rior to the standard involute profiles in terms of the bending strength

    文摘:分別用有限元和電阻應變片法對修形齒形和漸開線齒形進行齒根彎曲應力計算與實驗應力分析.結果證明在彎曲強度方面修形齒形比標準漸開線齒形更優越
  5. 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。
  6. Sequence comparison indicated that the nucleotide homologies between the ha gene and those from eight other h3 subtype sfv isolates from china are over 95 %, and nucleotide identities between h3 sfv isolates in china and a typical h3 subtype avian influenza virus ( aiv ) strain dkuk1 - 63 are 95 % to 100 %. these might tell us that the ha gene of all h3 subtype sives isolated in china was originally from aiv although the vaccine based on ha do not protect against different subtype of influenza virus, it can provide favorable resistance to infection with antigenic variants within a subtype

    通過與其它7株國內siv分離株和6株genebank中的h3流感病毒ha序列比較分析，結果表明分離自我國不同地區的8株h3siv核苷酸序列同源性均在95 %以上，且與禽流感病毒（ aiv ）經典代表株dkuk - 63序列同源性在95 - 100 %之間，證實我國h3sivha基因來源於禽的流感病毒。
  7. It is indicated in the test that the influence of loading to strain in the grout was about in the range of 5 ~ 6m, and very weak beyond 4m. the distributions of strain and bond stress in the grout are attenuated in the minus exponential rule

    試驗結果表明，加載對錨固段內的應變影響范圍大致在5 6m左右， 4m以外很微弱；錨固段注漿體內的應變與粘結應力分佈按照負指數規律衰減。
  8. . moreover, some samples appeared several active bands in the gel, which indicated the existence of different types of sod or multi - subunits of sod in these samples. the bacterial strain 276 is a gram - negative rod bacterium and there are more than 3 polar flagella, which observed after the gram ' s staining and flagellum staining

    同時，利用非變性聚丙烯酰胺凝膠（ page ）電泳后的凝膠顯色反應，發現一些樣品出現了多條活性帶，這可能是因為在這些細菌提取物樣品中含有不同類型的sod分子，或是同一類型的sod含有多個亞基組成。
  9. The sequence of quinolone resistant determing regions ( qrdr ) of gyrase subuint a of salmonella analysis indicated that the gyra gene of strain sll - 3 share 95. 8 % respectively identities with the sequence that griggs reported which showed a high homology between the strains

    對1株耐藥菌株的染色體pcr擴增產物進行了測序，與griggs等在genbank中注冊的沙門氏菌gyra基因qrdr的編碼序列進行比較，同源率為95 . 8 。
  10. Morphological properties and 16s rdna sequence analysis indicated that the strain is a novel species related to the genus myxococuus. the absorption by the myxococuus sp. nust03 is equilibrated in five minutes at ph 6. 0

    通過對菌株的形態結構、生理生化特性和基於16srdna序列的系統學分析初步認定此菌株為粘球菌屬的一個種（ myxococuussp . nusto3 ） 。
  11. The supernatant fraction and the precipitation fractions were analyzed by western blotfor strain dh5 a / pkkfpga, 5 - 10 % pga precursors formed as inclusion bodies in the cytoplasm while no inclusion bodies formed in the periplasm, this suggested most pga precursors were transported to the periplasm and matured to active pga and indicated that the maturation of pga in strain dh5 / pkkfpga was limited by the translocation step

    Western印跡分析表明對于菌株dh5 pkkfpga ， 5 - 10的原前體青黴g素酰化酶在胞內形成了包涵體，說明其成熟的限速步驟在胞內的運輸階段，而菌株dh5 psmlfpga則無明顯包涵體形成，說明菌株dh5 psmlfpga改善了青霉素g酰化酶的合成流，因而其表達能力高於菌株dh5 pkkfpga 。
  12. The results also indicated that the virulence of the most ibdv field collected in recent years was between the typical very virulent and standard virulent strains. a very virulent strain gx8 / 99 of ibdv was studied for its mortality in spf chickens and commercial egg - type chickens at different age inoculated with bursal suspension of 20 - 2000 eld50 in repeated experiments

    選擇致病性最強的來自廣西的gx8 99株，在對法氏囊懸液中病毒用雞胚半數致死量（ eld _ （ 50 ） ）定量測定后，在不同年齡的spf雞和商品代蛋用型塢多次重復地比較研究了該毒株的致病性。
  13. 16s rdna sequence analysis of three strains of 050642, 060386 and 060524 whose id50 is above 1200 indicated they also belong to streptomyces genus and strain 050642 is suspected to be a novel streptomyces. spp with the highest similarity to streptomyces colicolor, at 95 %

    對三株有較強活性的菌株050642 、 060386和060524進行了16srdna序列分析，初步確定這三株菌都屬鏈黴菌屬，其中菌株050642與其親緣關系最近菌株的相似性僅為95 ，極有可能是鏈黴菌屬的一個新種。
  14. The expression conditions of e2 gene in p. pastoris were optimized, the results indicated that the peak obtained after 72 hours ; pattern of inhibition / induction could improve expression level ; the best ph value were between 7. 5 and 8. 0 and the optimized methanol - induced concentration was 2 % - 3 % the e2 genes of the prevalent strain ( guangxi yulin strain ) and c strain derived from rabbit spleen tissue were amplified and cloned into e. coli the expression vector pproex - htb respectively, the recombinant plasmids pproex - gxyl and pproex - c were obtained and then were transformed into the dh5a e. coli competent bacteria respectively, the recombinant bacteria could express the major antigen region of e2 gene, the expression yields amount to 35 % and 38 % repectively

    豬瘟病毒ez基因的原核表達： pcr擴增出當前豬瘟流行野毒株，中國豬瘟兔化弱毒（ c株）兔脾組織毒ez基因的主要抗原區，將其克隆到原核大腸桿菌表達載體pproex htb中誘導表達，經sds page檢測表明，重組質粒能表達ez基因主要區蛋白， westernblot檢測表明，誘導表達蛋白與豬瘟陽性血清發生特異性反應，表達量為35和38 ，可用於基因工程診斷抗原。
  15. Sequence analysis indicated that the opening reading frame of ns1 gene is 1056nt in length, encoding 352 amino acids, identical to the sequence of strain sa 14 - 14 - 2 deposited in genbank. ns1 gene in the pmd18 - t - ns1 was cut by bamhi and hindiii, was cloned into the expression plasmid pet - 30b ( + ) treated with the same enzymes, resulting in a recombinant plasmid pet - 30b - ns1. the pet - 30b - ns1 was identified by pcr, restriction digestion, and sequencing

    通過序列分析結果表明， jev - ns1基因編碼區核苷酸序列長度為1056bp ，編碼352個氨基酸，序列分析和比較表明本實驗克隆到的ns1蛋白基因與genbank中收錄的疫苗株sa14 - 14 - 2的核苷酸序列一致，表明盡管該疫苗株在我國應用多年，但ns1基因並未發生變異，提示該疫苗株遺傳性狀比較穩定，是一株優良的疫苗株。
  16. The gene recombinant strain no. 42 ca n ' t generate ampramycin, which indicated that the cloned gene is involved in apramycin biosynthesis in s. tenebrarius

    通過接合轉移的方法將質粒pzxb014導入黑暗鏈黴菌h6中，篩選基因發生重組的菌株。
  17. The comparative analysis of sequences indicated that the sequences of meq in different pathotypes are relatively conserved and the homology of the amino acid sequences is very high. the significant differences include two mutations in both mdv - 1 vaccine strains cvi988 / rispens and 814 strain : the deletion of a proline ( no. l93aa ), and this mutation is just exactly located in a 15 - amino - acid ( eelcaqlcstppppi ) repeat sequence within the c - terminal transactivation domain of meq protein ; and a point mutation with a shift from alanine ( a ) of all virulent strains to serine ( s ) was occurred on the no. 71 aa

    結果發現， mdv不同致病型的meq基因序列相對比較保守，它們相互間核苷酸和氨基酸序列的同源性均很高；但是，與所有七個致瘤性的mdv毒株相比，二個型弱毒疫苗cv1988 rispens株和814株均出現了兩個特徵性的突變：即第194位的p缺失性突變和第71位氨基酸由a變成了s的位點突變；缺失性突變恰恰位於meq基因中轉錄激活域內的一個多脯氨酸的重復序列（ pppp ）之中。
  18. Using erwinia carotovora strain scg1 as pathogen, the effect of b. thuringiensis strain 4d1 culture was detected on the rot soft disease. the results indicated that 4d1 culture inhibited the pathogenicity of scg1 in 24 hours when the cell density of scg1 was lower than odeoonm = 0. 55, but when the incubation time after infection was longer than 24 hours, the effect decreased

    以胡蘿卜軟腐歐文氏菌菌株scg1為例，當菌株scg1的細胞濃度od _ （ 600nm ） < 0 . 55時，經蘇雲金芽胞桿菌菌株4d1培養物處理后感染馬鈴薯，在24小時內，可完全抑制軟腐病斑，但隨著培養時間的延長，其抑制作用逐漸減弱。
  19. In the same time, this paper applied the plane strain fem based on biot theory to analyzed calculated result and observation information hi scene. finally, this paper put forward a settlement forecast model based on the modified gaomujunjie method, using by inversion analysis theory to compare and analyze the settlement process of vhlcp. result indicated that the model inosculated with the fact data and the consolidation degree have finished 86 %, back - work settlement was 87mm

    最後，根據實測沉降資料，採用一維反演分析法，推導最終沉降量計算公式，結合改進后的高木俊介固結度計算方法，建立真空堆載聯合預壓的沉降預測模型，並根據計算結果，對比實際沉降過程，對比表明：所建沉降預測模型與實測數據吻合，由此所得現場試驗的地基平均固結度達86 ，剩餘沉降為87mm ，滿足高速公路質量要求。
  20. The stress - strain behavior of the remolding sample indicated that the failure of residual soil slopes is not caused by static liquefaction

    土體的應力應變特性表明土體破壞不是靜力液化機制所致。
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