芽胞體 的英文怎麼說

中文拼音 [yábāotǐ]
芽胞體 英文
brood gemma
  • 芽 : 名詞（植物剛長出來的可以發育成莖、葉或花的部分） bud; sprout; shoot
  • 胞 : Ⅰ名詞1 （胞衣） afterbirth2 （同一個國家或民族的人） fellow countryman; compatriot Ⅱ形容詞（同胞...
  • 體 : 體構詞成分。
  1. 3. the effect of sporulation - independent promotor on toxicity of natural strain in order to study the effect of sporulation - independent promotor ( p3a ), p3a was spliced with the cry1c gene, then inserted into the shuttle vector pht304, and then recombinated plasmid pbmb827 was obtained. after transferring pbmb827 into strain ybt - 1520, it was surprising that the transformants had almost no potency against all lepidopteran larvae tested

    3非依賴芽胞形成icp的cry3a啟動子（ p _ （ 3a ） ）對野生菌株特性的影響帶p _ （ 3a ）和cry1c基因的重組質粒pbmb827轉入ybt - 1520 ，轉化子對所測昆蟲的毒力下降非常明顯，芽胞和晶體也很難脫落。
  2. Two main parts were included in the present thesis. part i. cloning and expression cryigenes of bacillus thuringiensis in different host strains

    一、蘇雲金芽胞桿菌殺蟲晶體蛋白基因在不同受體菌中的表達1
  3. The results were unambiguous : two minutes of microwaing on full power mode killed or inactiated more than 99 percent of all the liing pathogens in the sponges and pads, although the bacillus cereus spores required four minutes for total inactiation

    結果是非常明了的：在高能量模式下經過兩分中微波可以殺死或者滅活99以上的所有在海綿和洗滌墊中的病原體，盡管蠟樣芽胞桿菌總體滅活時間需要4分鐘。
  4. A new resolution vector based on tnpi - mediated site - specific recombination system of b. thuringiensis transposon tn4430 was developed. the crylac10 or other target dna, and the gene ori1030, from a plasmid of wide type b. thitringiensis subsp

    利用轉座因子構建解離載體的可行性利用蘇雲金芽胞桿菌轉座子tn4430的解離區構建了解離載體。
  5. Kurstaki strain hd73, were inserted into two copy sets of res sites. the res sites have same direction. when - the recombinant plasmid was introduced into crystal negative b. thuringiensis host bmb171, antibiotic resistance genes and other non - 5, thuringiensis dna can be selectively eliminated after the selection by antibiotic resistance marker

    將crylac10基因或壯觀黴素基因和蘇雲金芽胞桿菌的質粒復制起始區oril030連接在一起，置於兩個同向的解離區之間，再將基因操作中所必需的大腸桿菌質粒復制起始區和抗生素標記基因等與之相連構成解離載體。
  6. The acrystalliferous and plasmid - free derivatives of bacillus thuringiensis were screened with ethidium bromide treatment, elevating growth temperature from 42 to 44 then to 46 by degrees, and treating it with 0. 05 % sodium docecyl sulphate ( sds ) as the plasmid - curing agent at 46

    分別用溴化乙錠誘變處理、逐級升溫培養以及用sds處理等三種方法對蘇雲金芽胞桿菌無晶體（ cry ~ - ）和無質粒突變株進行了篩選研究。
  7. Furthermore, we found some embryogenesis - related proteins during somatic embryogenesis of aralia elate ( miq. ) seem, which promoted the occur and development of embryoids

    在龍芽?木體細胞胚發生過程中，我們發現了若干胚胎發生相關蛋白。
  8. Seem in order to explain the molecular mechanism of somatic embryogenesis. in the light of the expression model, many soluble proteins were expressed dynamically in an specially temporal - spatial sequence

    龍芽?木體細胞胚發生過程中可溶性蛋白表達模型的建立，從整體上體現了可溶性蛋白表達的時空特異性。
  9. In this study, two kinds of specific promoter of b. thuringiensis : cry 3a promoter and btl - btll promoter were chosen to construct fusion genes to drive the expression of gfp gene in b. thuringiensis strain

    本研究在構建蘇雲金芽胞桿菌質粒克隆載體pbmbi105的基礎上，克隆了菌株ybt一1520的質粒，獲得6 . 6kb的dna片段。
  10. The research results are summarized as following : 1. the relationship between gene types and the toxicity against s. exigua in order to construct satisfactory genetically engineered strain, it is first necessary to understand the relationship between gene types and the toxicity. nine strains containing crylc were chosen for study for this purpose

    研究結果總結如下： 1菌株對甜菜夜蛾的毒力與基因類型的關系pcr擴增檢測了九個蘇雲金芽胞桿菌菌株所含殺蟲晶體蛋白（ insecticidalcrystalprotein ， icp ）基因，根據擴增結果將它們分為5種基因類型。
  11. The recombinant plasmids pbmb121l, pbmb9821l and pbmb986l were constructed after transferring bacillus thuringiensis icps gene crylaal, crylaclo and crylca from their original plasmid vectors to different plasmid vector. the relevant recombinant strains were obtained after introducing the 3 recombinant plasmids into bacillus thuringiensis plasmid - free mutant strain 8mb 171 by electroporation. the transformation and expression properties of 8mb 171 were studied

    通過將蘇雲金芽胞桿菌殺蟲晶體蛋白基因cry1aal 、 cry1ac10和cry1ca轉移至不同質粒載體上，分別構建了重組質粒pbmb121l 、 pbmb9821l和pbmb986l ，並分別導入無質粒突變株bmb171 ，篩選得到攜帶相應icps基因的重組菌株。
  12. 4. effect of resolution vector on the expression of pesticidal crystal protein genes this work successfully introduced pesticidal crystal protein genes into crystal negative strain bmb171 by using resolution shuttle vectors. after resolution, the expression of cry1ac and cry 1c genes have no obvious change, but the expression of cry3a genes has great increase in the same condition

    解離反應對殺蟲晶體蛋白基因表達的影響成功地利用解離載體將crylac10 ， crylc和cry3a基因導入蘇雲金芽胞桿菌無晶體突變株， crylac和crylc基因解離前後的表達量和殺蟲毒力未見明顯變化， cry3a基因在相同條件下則表達量有所提高，至於為何只對基因cry3a有作用尚不清楚，國內外也未見有人作相關報道。
  13. Microcalorinetric study on b. thuringiensis by using an lkb - 2277 bioacitivity monitor, the thermogenic curves of different b thuringiensis strains ybt - 833 and ybt - 833 - 2 - i, have been determined. the metabolism heat output revealed the heat output was correlated to the yield of the protein, the higher yield protein, the less heat output. a microcalorimetric technique based on the bacterial heat - output was explored to evaluate the effect of various promoters and different plasmid original replicons on the expression of gfp

    不同蘇雲金芽胞桿菌基因工程菌的微量熱變化利用生物活性檢測器lkb - 2277研究殺蟲晶體蛋白含量不同的兩株菌ybt - 833 、 ybt - 833 - 2 - 1的熱動力學變化，發現菌體合成殺蟲晶體蛋白的過程是一個耗能的過程，殺蟲晶體蛋白產量高的菌株向外釋放的代謝熱少，反之亦然。
  14. The dissertation mainly concerns the construction of resolution vector based on bacillus thuringiensis transposon tn4430. the research results are summarized as following : 1

    本論文主要圍繞構建蘇雲金芽胞桿菌解離載體而開展研究工作，研究結果如下： 1
  15. The dissertation mainly concerns the construction of resolution vector with green fluorescent protein. the research results are summarized as following. 1

    本研究主要圍繞構建高效表達的gfp解離載體標記蘇雲金芽胞桿菌而開展的研究工作，主要研究結果如下： 1
  16. The optimized parameters of high - frequency in bacillus thuringiensis plasmid - free mutant bmb171 by electroporation was studied. it showed that a highest electro - transformation frequency could be obtained, when sg solution was used as the buffer, and a 10. 0 kv / cm of field strength, one time of pulse as well as a growth phase of recipient cells at the exponential phase ( od650nm value was 0. 2 - 0. 3 ) were selected

    對用電脈沖法轉化蘇雲金芽胞桿菌受體菌bmb171優化條件的研究結果表明，採用sg溶液作電脈沖緩沖液，用10 . 0kv cm的脈沖場強和1次電脈沖（ 4 . 6ms ） ，以及採用對數前期（ od _ （ 650 ）約0 . 2 0 . 3 ）收獲的受體菌，可以達到最高轉化頻率。
  17. 1. expression of cry genes located in native plasmid in different flagella serotype strains to study cloning and expression of icps genes, an ecor i - f fragment of cryla ( a ) gene from pesi was inserted into pselect - 1 with t7 rna polymerase promoter in vitro. the plasmids of bacillus thuring fensisybt - 803 and ybt - 791 were analyzed by southern hybridization using an rna probe of ecori - f fragment and by pcr identification with cryl mixture primers

    將cry基因的高保守區的cry a （ a ） ecog - f片段插入帶有t7rna聚合酶啟動子的質粒pselect - 1 ，獲得了能在體外轉錄的rna探針載體pbpl - 1 ，用該載體制備的rna探針具有特異強，背景清楚，省時省力等優點，已成功地用於蘇雲金芽胞桿菌的分子生物學研究和特異菌株的篩選。
  18. Aralia elate ( miq. ) seem is a kind of uncultivated vegetable from the mountain changbai. the process of somatic embryogenesis includes morphogenesis stage of calli, conversion stage of embryonic calli, embryogenetic stage and regeneration stage of plant in aralia elate (

    本論文採用sds -聚丙烯酰胺凝膠電泳技術，對龍芽?木體細胞胚發生過程中愈傷組織形態建成、胚性愈傷轉化、胚狀體發育和植株再生四個階段的可溶性蛋白的動態變化進行分析。
  19. Expression of aii gene expanded from vegetative stage to early stage of sporalation

    Aii基因位於染色體上，在培養初期開始轉錄，一直延續到芽胞形成前期。
  20. The dynamic changes of soluble proteins occurring in aforesaid stages were analyzed by sds - page. we established a expression model of specific proteins occurring in somatic embryogenesis of aralia elate ( miq. ) seem on the grounds of the sds - page result

    根據可溶性蛋白動態變化的特點，我們建立了龍芽?木體細胞胚發生過程的蛋白質表達模型，並找到了一些與體細胞胚發生相關的特異性蛋白。
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