抑菌測定 的英文怎麼說

中文拼音 [yìjūncèdìng]
抑菌測定 英文
bacteria inhibition assay
  • 抑 : Ⅰ動詞（向下按; 壓制） restrain; repress; curb Ⅱ連詞[書面語]1 （表示抉擇） or 2 （表示轉折） but3 ...
  • 菌 : 菌名詞1. （蕈） mushroom2. （姓氏） a surname
  • 測 : 動詞1. （測量） survey; fathom; measure 2. （測度; 推測） conjecture; infer
  • 定 : Ⅰ形容詞1 （平靜; 穩定） calm; stable 2 （已經確定的; 不改變的） fixed; settled; established Ⅱ動詞...
  • 測定 : determine; determination; setting-out; admeasurement; assignment; assay; finding
  1. In order to analyze the differences of the content of ergosterol in the imazalil - sensitive and imazalil - resistant isolates of p. digitatum, the technology of hplc was used. the results showed that the contents of ergosterol between imazalil - sensitive and imazalil - resistant isolates were not significantly defferent ( p = 0. 05, dmrt ) when they grew in the medium without imazalil. interestingly, when imazalil ( 0. 1 # g / ml ) was added to the medium, the content of the ergosterol in imazalil - resistant isolate ( pd07 ) was significantly higher than that in imazalil - sensitive isolate ( pd23 ) ( p = 0. 05, dmrt )

    結果表明，在抗性菌株pd07不加抑霉唑的情況下， pd07和pd23中游離麥角甾醇的含量採用duncan ' s新復極差測驗在5水平沒有明顯差異；但當pd07中加入0 . 1 g ml抑霉唑時，三次重復測定結果顯示抗性菌株pd07中麥角甾醇的含量明顯地要比敏感菌株pd23中的含量高，而且兩者在5水平上差異顯著。
  2. Based on the extensive studies of subtilisin - like protease ( prl ) of metarhizium anisopliae, extracellullar serine protease is suggested to be a key enzyme involved in the fimgal penetration to invertebrates. the investigation of serine protease in the nematode infected by owvtl may help to understand the mechanism of nematophagous fimgi as biological control agents. a 3l kda serine protease was isolated and purified from the liquid culture of h rhossiliensis owvtl challenged with nematode panagrellus redivivus

    本研究利用線蟲誘導下owvt - 1菌株液體發酵，通過粗分級分離、離子交換層析和凝膠過濾層析分離提純了一個分子量為31kda的絲氨酸蛋白酶，生物學測定表明其對大豆胞囊線蟲二齡幼蟲具有致死作用，同時測定了該酶理化特性，酶活力在75附近酶活力最高，隨著ph的增加酶的穩定性升高，與膽堿酯酶具有相似的ph曲線，對特異性底物aape （ suc - ala - ala - pro - glu - pna ）具有作用， ssi和ci - 2抑制該酶的活性。
  3. The fungistasis of dichloromethane extracts 7 plants from were tested by growth rate method with the common fungi such as rhizoctonia solani, cladosporium ucumerinum, alternaria solani and fusarium oxysporium

    摘要用生長速率法以辣椒絲核病菌、黃瓜黑星病菌、番茄早疫病菌和黃瓜枯萎病菌為供試菌種，對7種植物的12種二氯甲烷提取物進行了抑菌活性測定。
  4. But four enterococcus grew quickly and hadn " t delaying period, the final period of logarithm growing of all tested strains were 12 hour for i acidophilus pb1 and a878 ; 24 hour for bifidobacteria pba and inf ; 8 - 10 hour for enterococcus ml, pb2, a30, a31 and bacillus abticism2 the growth inhibition of escherichia coli, shigellosis, salmonell by the fermented liquor of eight probiotics bacteria was tested

    確定各菌株對數生長期末期分別為： pb1和a878 ： 12h ； inf和pba ： 24h ； pb2 、 m1 、 a30 、 a31 、 m2 ： 8 - 10h 。採用牛津杯法測定八種潛在益生菌對大腸桿菌、痢疾桿菌、沙門氏菌的抑制性，結果表明，嗜酸乳桿菌pb1 、 a878和雙歧桿菌pba 、 inf具有較強的抑菌能力，對三種致病菌能夠形成明顯的抑菌圈，而且對三種致病菌的抑菌能力明顯不同。
  5. Wood preservatives - determination of the effectiveness against soft rotting micro - fungi and other soil inhabiting micro - organisms

    木材防腐劑.防腐劑抗輕腐蝕微生黴菌和其他土壤抑制微生物有效性的測定
  6. The inhibition mechanisms of pb1, a878, pba, inf were some organic acids and antibacterial substance in fermented liquor. l. acidophilus strains pb1, a878 mixed with enterococcus strains ml, pb2, a30, a31 respectively in the ratio of 1 : 1 in the mrs cultures, co - cultural and single liquor inhibition to the enterpathogens were tested in the terminal fermentation

    將pb1和a878分別與m1 、 pb2 、 a30 、 a31以1 : 1的比例混合發酵后，測定聯合菌株對致病菌的抑制性，結果表明pb1與各球菌聯合后，可以互利生長，其中復合較好的為pb1與m1和a30 。
  7. Optimization of process for ultrasonic extraction and primary determination of bacteriostatic activity of protein from flos trollii chinensis

    金蓮花蛋白超聲提取工藝優化及其抑菌活性的初步測定
  8. In escherichia coli, arog gene encodes phenylalanine - sensitive 3 - deoxy - d - arabino - heptulosonate - 7 - phosphate synthase isoenzyme arog that catalyzes the first committed step of shikimate pathway. here we study the essential amino acid residues involved in the formation of feedback inhibition site of arog, and the effects of n - terminus on feedback inhibition and its quaternary structure, and the importance of the structural " d2 " symmetry to allosteric inhibition

    本博士論文工作以大腸桿菌k - 12來源的arog為研究對象，通過定點突變、反饋抑制實驗和酶學動力學參數的測定，深入地研究了arog的反饋抑制位點的特性，並對arog的n -末端在反饋抑制機理和維持穩定四級結構中的作用，以及蛋白質結構的「 d2 」對稱性對酶功能的重要性等進行了具體的研究。
  9. Standard test method for determining bacterial retention of membrane filters utilized for liquid filtration

    測定液體過濾用膜過濾器的抑菌能力的標準試驗方法
  10. After plasmid and cherosome dna extraction and purification, the gyra of 16 isolates of salmonella gene was amplified by polymerase chain reaction ( pcr )

    測定了16株致病性沙門氏菌對12種抗菌藥物的最低抑菌濃度（ mic ） ，依照美國臨床實驗室標準委員會（ nccls ）標準（ 1990 ）判定菌株耐藥性。
  11. . water quality - determination of the inhibitory effect of water samples on the light emission of vibrio fischeri luminescent bacteria test - method using liquid - dried bacteria

    水質.水樣品對fischeri弧菌光發射抑制效果的測定
  12. . water quality - determination of the inhibitory effect of water samples on the light emission of vibrio fischeri luminescent bacteria test - method using freshly prepared bacteria

    水質.水樣品對fischeri弧菌光發射的抑制效果的測定
  13. 1. overexpression of the rate - limiting enzyme genes of e. coli strain e. coli w3110 chromosome dna and plasmid pg908 dna were separately used as template to amplfy genes arob and arog by pcr, the dna sequencing showed that the cloned genes were in agreement with the reported sequences

    大腸桿菌arog 、 arob基因的克隆與表達分別以大腸桿菌（ e . coli ） w3110染色體dna和質粒pg908dna為模板，用pcr方法擴增得到了arob基因和抗反饋抑制的arog基因，序列測定與文獻報道一致。
  14. Microplate luminometry for toxicity bioassay of environmental pollutant on a new type of fresh water luminescent bacterium vibrio - qinghaiensis sp. - q

    測定環境污染物對青海弧菌發光強度抑制的微板發光法研究
  15. The antibacterial activity test indicated that the ligands l1 ~ l4 and their complexes y1 ~ y ` 0 have good antibacterial activities against e. coli and s. aureus, in which the co ( ii ) complex is the best

    抑菌活性測定結果表明化合物對金黃色葡萄球菌和大腸桿菌均有一定的抑菌活性，其中以鈷配合物的抑菌活最好。
  16. The positive transformants with the integrates mn - sod gene was identified by zeocin - resistance, pcr screening and expression in p. pastoris. the recombinant mn - sod protein was successfully expressed in pichia pastoris based on the evidences that a relative molecular weight about 23kd appeard in sds - page, the obvious activity of sod existed in native - page and enzymatic activity test, and mn - sod activity was specific base on the inhibition with the mixture of chloroform - enthanol ( 3 : 5 / v : v ) and potassium cyanide. two secreted plasmids ppiczaa - sodm18 and ppiczaa - sodc were constructed and after there linearization were transferred into chromosome of pichia pastoris gs115 by electroporation

    Pcr鑒定及mut表型分析進一步說明，目標基因已經重組到宿主菌基因組染色體上； 0 . 5甲醇誘導表達后， sds - page結果顯示，表達的蛋白相對分子量約為23kd ，活性電泳出現明顯活性條帶；酶活性測定顯示，重組菌株sod活性比對照提高5倍左右；氯仿-乙醇（ 3 : 5 v : v ）和kcn （ 5mmol l ）抑制反應進一步證明，所表達的sod為錳超氧化物歧化酶。
分享友人
分享到 Line

分享到臉書