芽晶 的英文怎麼說

中文拼音 [yájīng]
芽晶 英文
germ crystal
  • 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
  • 晶 : Ⅰ形容詞（光亮） brilliant; glittering Ⅱ名詞1. （水晶） quartz; （rock） crystal 2. （晶體） any crystalline substance
  1. Fig. 4 cholesterol granuloam in early stage. the granulation tissue matrix containing chronic hemorrhage, fewer cholesterol crystals and multinucleated giant cells ( he 200 )

    3成熟膽固醇肉芽腫：炎性肉芽組織基質中含有大量膽固醇結晶和多核巨細胞（ he染色100 ） 。
  2. 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。
  3. The recombinant b. thuringiensis subsp. israelensis b - pmpx2 can produce a rhombus crystalline inclusion body during its sporulation sds - page analysis proved that cytlaa had overexpressed during the sporulation of the recombinant. it was found that b - pmpx2 strain remained stable toxicity, whatever during vegetative phase or sporulation phase, which was similar to the expression of mtxl gene in the strain of protease ( s ) - deficient b. sphaericus

    同時，將來源於蘇雲金芽孢桿菌以色列亞種（ b . thuringiensissubsp . israelensis ， b . t . i ）的cytlaa基因和p20伴侶蛋白基因克隆連接到質粒pmt9中，並轉化到蘇雲金芽孢桿菌無晶體型中得到重組轉化子b - pmpx2 ，電鏡觀察發現重組轉化子b - pmpx2形成一菱形晶體。
  4. 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
  5. After the acet is vaporized, the active substance in water is gotten. and which is vaporized at low temperature. then the crude active substance is purified by column chromatography on sephadex g - 75. after a series of purifications again, we could get some white powder at last. though the active substance is diluted to50 g / ml, the activity is still checkeded - up through phyto phtnora casicileon. the purified active substance is insensitive to heat, resistant to chloroform 、 ethanol and the orhers. in addition, the active substance is sensitive to high ph ( 10 ~ 14 ), but it is not sensitive to low ph ( 1 ~ 5 ). furthermre, when the ph is made to low again, the activity of it ' s comes back

    用蒸餾水對菌體稀釋；加入適量吸附樹脂在150rpm 、 28下振蕩吸附4h ， 80 %的丙酮解吸，過濾解吸液得到活性物質的澄清溶液，旋轉蒸發儀旋轉蒸發去處丙酮，經sephadexg - 75分子篩層析得單一活性峰，收集峰值部分樣品液經冷凍乾燥得到淡褐色粉末，該活性物質用丙酮充分洗滌、甲醇-乙醚重結晶獲得略帶微黃的白色粉末，該活性物質50 g / ml仍可對蘇雲金芽孢桿菌hd - 1產生明顯的抑制作用。
  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. It is easily convert your mobilephone communication into this in - car solution, talking through its build - in high quality speaker and external microphone

    易地將您手機上的通訊轉移到此耳機上，本產品內含csr bc02藍芽晶片及
  8. 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。
  9. 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。
  10. 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。
  11. 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。
  12. Effect of cry3a promoter on expression by using resolution vector, the cry1ac and cry1c genes with cry3a promoter or it itself promoter were introduced into b. thuringiensis crystal negative strains. the expression of these strains is quit similar, however, the expression of cry 1 ac and crylc with different promoter in same cell has no complete inhibition

    Cry3a啟動子對基因表達的影響利用解離載體將帶cry3a啟動子的crylac10和crylc基因導入蘇雲金芽胞桿菌無晶體突變株，基因的表達和殺蟲活性與帶自身啟動子的基因的表達相近。
  13. Kustaki : ori44, oriw30 and ori2062 were chosen to construct the gfp resolution vector. there were 9 kinds of gfp resolution vector. all of the recombinant plasmids were introduced into crystal negative b. thuringiensis 8mb 171. the fluorescence of the 9 kinds engineered strain can be detected by the fluorescent microscope

    將得到的9種gfp解離載體電轉化到蘇雲金芽胞桿菌無晶體突變株bmb171中，熒光顯微鏡鏡檢顯示9株含gfp的蘇雲金芽胞桿菌重組菌在波長為300nm - 510nm的激發光下可發射綠色熒光。
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