青變菌 的英文怎麼說

中文拼音 [qīngbiànjūn]
青變菌 英文
blue-stain fungi
  • 青 : Ⅰ形容詞1 （藍色或綠色） blue or green 2 （黑色） black : 青布 black cloth; 青牛 black ox3 （年輕...
  • 菌 : 菌名詞1. （蕈） mushroom2. （姓氏） a surname
  1. E. coli xl1 - blue cells were tansformed by psurfpga and phages were rescued by m13ko7 helper phage particles. results showed that the heterodimeric enzyme was expressed as a fusion protein that matures to an active biocatalyst connected to the coat protein of phage fd

    以構建的噬菌粒psurfpga轉化具有琥珀突變的大腸桿菌xl1 - blue ，以輔助噬菌體m13k07超感染，進行青霉素g酰化酶基因的表達和在噬菌體表面的展示。
  2. This fact suggested that dndb and dndc were directly involved in the novel dna modification in wild type s. lividans

    這兩個突變株均喪失了dnd表型，暗示這些基因與變鉛青鏈黴菌的異常修飾直接相關。
  3. Hau3r gene of s. lividans 1326 is directly related to its resistance to actinophage hau3

    野生型變鉛青鏈黴菌1326中的hau3 ~ r基因與1326對噬菌體hau3的抗性直接相關。
  4. When phz2057 was introduced into s. lividans zx1, it could confer partial resistance to actinophage hau3 on s. lividans zx1

    將phz2057轉入變鉛青鏈黴菌zx1 ，能賦予變鉛青鏈黴菌zx1對噬菌體hau3的部分抗性。
  5. Analysis of the sequence revealed that adda resembled nifs of nitrogen - fixing bacteria and dnda. the entire add gene cluster showed 78 % identity to dnd gene cluster from s. lividans

    同源性比較揭示add基因簇的adda基因與固氮酶基因nifs高度同源， add與變鉛青鏈黴菌dnd核苷酸的同一性為78 。
  6. Through screening a lot of mutants with the method of transparent zones and culture filtrate, the best four were obtained with high - yield of stable phb depolymerase, named as 02, 04, 09 and 14

    以青黴（ penicillium . sp ） ds9701為出發菌株，通過紫外線誘變分生孢子，採用透明圈初篩和搖瓶培養復篩的方法，獲得4個能穩定遺傳的phb解聚酶高產菌株。
  7. The study shows that the early and late seed rains of constructive tree species in evergreen broadleaved forest at chongqing simian mountain had no activity. the bigger the seeds of the species and the earlier or later the seeds of the species matured, the higher the proportion of the seed rain damaged by animals. the quantitative variation of seed rain, active seed rain and seed bank did not take place at the same time. at early time, the number of seed banks of castanopsis fargesii, lithocarpus glabra, quercus myrsinrefolia, castanopsis plasyacantha, cinamomum subavenium. which own more active seed rain increased by geomitric series. the seed banks of castanopsis orthacantha and schima argentea were small, only survived a short time, and did not sprout next year. the quantitative dynamics of seed banks and their increasing or decreasing rates were decided by the proportion damaged by animals, dying speed of seeds and their resistance to pathogens and adverse circumstances, and the state of seed germination

    對重慶四面山常綠闊葉林建群種種子雨、種子庫的研究表明，建群種早期和晚期的種子雨無活力;種子偏早或偏晚成熟及大籽粒的樹種，其種子雨被取食的比例大;種子雨、有活力種子雨、種子庫三者的數量變化不一致;有活力種子雨量較大的栲、石櫟、小葉青岡、扁刺栲、香桂等，其種子庫密度在早期以近幾何級數的方式增長，元江栲、銀木荷種子庫小，存在時間短，翌年無一年生萌發苗;種子庫數量動態、消減率動態決定於種子被取食的強度、種子衰老的速度以及種子對病菌、逆境的抗性和種子萌發的整齊性
  8. Wait for the green vegetables to change dry, cut into the segments, put on thick salt, mix with the hot pepper, wild pepper, ginger, eight capes, xiaogoxiang and anticipate these seasonings of the wine, since can suppress the germ, antisepsis, and then increased various flavor

    待青菜變蔫后，切段，撒上粗鹽，拌以辣椒花椒生薑八角小茴香和些許料酒這些作料，既可抑菌防腐，又增添了各種香味。
  9. Streptomyces low copy number plasmid scp2 * is also employed for the cloning and recovery of large dna fragment from streptomyces. as scp2 * can accommodate large dna insertions and is efficiently transmissible among its permissive hosts such as s. lividansbut seemed to be unable to replicates in streptomyces sp. fr - 008, it might be a suitable vector for the cloning of the entire fr - 008 pks gene cluster through gene replacement followed by conjugation with 5

    Scp2 *可以在變鉛青鏈黴菌等許可宿主內復制並在許可宿主間有效轉移，但似乎不能夠在鏈黴菌fr - 008中復制，因此可能適合於在鏈黴菌fr - 008中通過進行基因置換及隨后的鏈黴菌fr - 008和變鉛青鏈黴菌間的接合過程來克隆完整的fr - 008生物合成基因簇。
  10. The dnd cluster seemed to express when it was carried by the high copy - number plasmid because complementation of individual dnda, dndb or dndc mutation could be observed and such expression did not seem to influence the normal dnd expression in wild type s. lividans 1326

    而在高拷貝質粒上的dnd基因似乎是李愛英變鉛青鏈黴菌dna異常修飾系統的分子生物學研究能表達的，因為它能紅補分別在dn劇、 dndb和咖jc發生單個基因突變的菌株，而且這種表達似乎也不會影響野生型菌株1326中原有的dnd基因簇的表達。
  11. S. lividans mutant strains zx1 ( dnd cluster deleted ) and zx64 ( dnda disrupted ) had pleiotropic mutations including low mel expression and poor sporulation. it was speculated that dnda together with its downstream dna ( 2. 5kb ) might be involved in these two phenotypes because dnda together with its downstream dna could restore normal sporulation and mel expression to zx64, while dndb and dndc had no such effect because lai and la2 showed no obvious difference in these two phenotypes from wild type s. lividans 1326

    另外通過比較這幾個突變株及野生型菌株在產孢和黑色素基因（ mel ）表達方面的差異，推測dnda及其下游區域與變鉛青鏈黴菌的產孢和刺激外源黑色素基因的表達有關，而dndb和dndc則與之無關，因為la1和la2在這兩種表型上與野生型菌株無明顯差異。
  12. Using these vectors, expression of the pks gene was achieved both in streptomyces lividans and in e. coli in a heat - dependent manner, suggesting that the lambda promoter and temperature - sensitive lambda represser functioned in s. lividans as well as in e. coli

    利用這些質粒在變鉛青鏈黴菌和大腸桿菌中均表達出pks蛋白，兩種宿主中的表達都是熱依賴的。暗示噬菌體啟動子和溫敏型阻遏物在變鉛青鏈黴菌和大腸桿菌中都具有功能。
  13. In this study, the suitable parameters for the introduction of plasmids phz1358 and pset152 into s. nanchangensis ns3226 from e. coli were tested for developing an conjugation system for s. nanchangensis ns3226. a dnd gene cluster, which encodes an unknown modification system for 5 hvidans 1326 and renders its dna susceptible to site - specific double - strand dna cleavage during electrophoresis was conjugated from e. coli into s. nanchangensis ns3226

    將克隆在整合型載體pset152上的變鉛青鏈黴菌1326的dnd基因簇通過接合轉移導入野生型南昌鏈黴菌ns3226中進行異源表達，觀察到接合轉移子的dna獲得了在含fe ~ （ 2 + ）的電泳緩沖液中電泳時降解的表型。
  14. Eleven strains of penicillium, i. e. pt95 strain and its 4 mutants as well as 6 standard strains bought from institute of microbiology, academia sinica, have been analyzed for their rapd genotype

    運用rapd技術對pt95菌株、 4株pt95的突變株和6株標準青黴菌株進行了比較。
  15. Also the ci represser was expressed, presumably from its own phage promoter and prevented transcription from pr at low temperature. moreover, s. lividans strains expressing the c. 100 kda pks were different in sporulation and antibiotic production compared to strains without the 2. 7 kb pks gene, suggesting that the pks protein was active in an unknown manner in streptomyces

    表達pks的變鉛青鏈黴菌菌株在孢子形成和抗生素產生方面與沒有2 . 7kbpks基因的菌株相比較是有區別的，因而推測在鏈黴菌中表達的雙功能結構域pks蛋白具有活性。
  16. The expression of hau3r gene was leaky in s. lividans zx57, and hau3r gene was highly expressed when zx57 ( phz2085 ) was induced with thiostrepton at the concentration of 5 g / ml

    克隆的hau3 ~ r基因在變鉛青鏈黴菌zx57中獲得高效表達，且以可溶形式存在。
  17. No, she repeated, and continued sauntering on, pausing, at intervals, to muse over a bit of moss, or a tuft of blanched grass, or a fungus spreading its bright orange among the heaps of brown foliage ; and, ever and anon, her hand was lifted to her averted face

    「不， 」她又說，繼續向前閑蕩著，間或停下來，望著一點青苔，或一叢變白的草，或是在棕黃色的成堆的葉子中間散布著鮮艷的橘黃色的菌沉思著，時不時地，她的手總是抬起到她那扭轉過去的臉上去。
  18. This unusual modification causes wild type s. lividans 1326 dna sensitive to site - specific oxidative double - strand cleavage ( dnd phenotype ). preliminary study revealed that such dna modification involves incorporation of sulphur. the entire functional dnd cluster, 8. 3kb in size, including 3 orfs - dnda, dndb and dndc was involved in this dna modification

    野生型變鉛青鏈黴菌具有一種不同於甲基化修飾的新型dna硫修飾系統，使dna在電泳時易遭到氧化雙鏈切割而導致降解（ dnd ， dnadegradation ）表型（ zhouetal . ， 1988 ， 1994 ， 1999 ） 。
  19. Phz621 - phz622, the new gene replacement vector system, had been constructed through the insertion of the 1. 0kb and 1. 4kb flanking sequences of hau3r gene from wild - type s. lividans in the same natural orientation

    預期在攜帶有大插入片段的基因置換yac分子進入野生型變鉛青鏈黴菌后， yac分子將通過1 . 4kb或1
  20. The application of scp2 * derivied vectors requires that the physical map of a specific gene cluster is known and scp2 * derivatives are suicidal in the host earring the gene cluster

    在新載體系統phz能1一phz622中，我們不但同向插入了來自於野生型變鉛青鏈黴菌中hau3r基因兩側的1
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