glucuronidase 中文意思是什麼

glucuronidase 解釋
葡糖醛酸酶
  1. Β-glucuronidase is a notable exception.

    -葡糖苷酸酶是一個值得注意的例外。
  2. Deduced amino acid sequence of s1, s2, pvin were also highly homologous each other ( 98 %, 99 % in each case ). the stilbene synthase genes were excised from the plasmids by bamh i and sac i digestion and intergrated into a binary vector, pbi121 and pev2, from which the p - glucuronidase ( gus ) gene sequence had been removed by the same digestion to prepare a 35s promoter - stilbene synthase 2 - nopaline synthase polyadenylation site construct and a tfp2 promoter - stilbene synthase 1 - nopaline synthase polyadenylation site construct. the recombinant plasmids were called pbs2, pev2s 1. respectively

    用bamhi和saci同時酶切ps2 （ s2表示來自雷司令的芪合酶基因） 、 ps1 （ s1表示來自粉紅玫瑰的芪合酶基因）以及pbi121 、 pev2 ，使得s2 、 s1分別插入替代pbi121 、 pev2中的gus基因，構建成植物表達載體pbs2 、 pev2s1 ， pbs2中含camv35s組成型啟動子，使s2基因能在番茄植株的各個部位表達； pev2s1則含有果實特異性啟動子tfp2 ，使s1基因只在番茄果實中表達。
  3. We clone a 1. 3kb promoter sequence of the homologous gene in arabidopsis by pcr. this promoter is shown to direct the specific expression of the reporter gene, b - glucuronidase ( gus ), in trichomes of arabidopsis. promoter deletion analysis reveal that the region from - 300 - - 1 bp is sufficient to direct trichome - specific expression

    對其進行缺失突變，構建5個缺失表達載體轉基因擬南芥，葉片gus定量測定分析表明- 300bp ? - 1bp序列就可以指導gus基因在表皮毛細胞中特異表達，說明這段序列可能含有指導此啟動子在擬南芥表皮毛細胞進行特異表達的核心序列。
  4. Agobacterium tumefaciens strain a311 carrying the plant tranfer vector pb1121, which contains the neomycin phosphotransferasell gene ( nptll ) and p - glucuronidase reporter gene ( gus ) both under the control of the camv 35s promoter, was used in the establishment of the genetic tranformation of white clover

    選用苗齡4 5天的帶柄子葉作為外植體，先將外植體預培2天，再與根癌農桿菌a311共培養3 4天後，轉入附加有40mg l ~ （ - 1 ）卡那黴素和400mg
  5. Distribution of - glucuronidase activity in macaca mulatta tissues

    葡糖醛酸酶在恆河猴組織中的分
  6. Microbiology of food and animal feeding stuffs - horizontal method for the enumeration of - glucuronidase - positive escherichia coli - colony - count technique at 44 c using 5 - bromo - 4 - chloro - 3 - indolyl - d - glucuronide

    食品和動物飼料的微生物學.葡糖苷酸酶陽性大腸桿菌計數的水平方法. 44下用5溴- 4氯3吲哚- - d葡糖苷酸的菌落記數技術
  7. Microbiology of food and animal feeding stuffs - horizontal method for the enumeration of - glucuronidase - positive escherichia coli - colony - count technique at 44 c using membranes and 5 - bromo - 4 - chloro - 3 - indolyl - d - glucuronide

    食品和動物飼料的微生物學.葡糖苷酸酶陽性大腸桿菌計數的水平方法. 44下用隔膜和5溴- 4氯3吲哚- - d葡糖苷酸的菌落記數技術
  8. Microbiology of food and animal feeding stuffs - horizontal method for the enumeration of beta - glucuronidase positive escherichia coli using 5 - bromo - 4 - chloro - 3 - indolyl beta - d - glucuronide by colony count technique at 44 oc - routine method

    食物和動物飼料的微生物學. 44時通過菌落計數法用5 -溴- 4 -氯- 3 -吲哚- d -葡糖苷酸對-葡糖苷酸酶陽性大腸桿菌計數的水平法.常規法
  9. Microbiology of food and animal feeding stuffs - horizontal method for the enumeration of b ? ta - glucuronidase positive escherichia coli - part 1 : colony - count technique at 44 o c using membranes and 5 - bromo - 4 - chloro - 3 - indolyl beta - d - glucoronide

    食品和動物飼料的微生物學. -葡糖苷酸酶陽性大腸桿菌計數的水平方法.第1部分: 44時用薄膜材料和5 -溴代- 4氯- 3 -吲哚基- d -葡糖苷酸的菌落計數技術
  10. Microbiology of food and animal feeding stuffs - horizontal method for the enumeration of b - glucuronidase - positive escherichia coli - part 2 : colony - count technique at 44 oc using 5 - bromo - 4 - chloro - 3 - indolyl b - d - glucuronate

    食品和動物飼料的微生物學. b -葡糖苷酸-陽性大腸桿菌計數的水平方法.第2部分: 44時使用5 -溴代- 4 -氯- 3 -吲哚b - d -葡糖苷酸的計群技術
  11. Fig. 2 the changes of myocardial beta - glucuronidase of rats after 4000 - 4500m running on treadmill. * p < 0. 05 compared with control group

    圖2運動后大鼠心肌組織葡萄糖醛酸酶活力的動態變化。運動后即刻組酶活力顯著增高，運動后3小時組和運動后24小時組酶活力進一步增高。
  12. In transgenic tobacco plants, the analysis of transient expression by monitoring 3 - glucuronidase activity revealed that a chimeric gene construct containing a 1. 2 kb pdf1. 2 promoter fused to a gus reporter gene was induced by meja

    （ 1 ）從擬南芥基因組中擴增出長度約為1200bp的pdf1 . 2啟動子，與gus構建的融合基因在煙草中的表達受meja誘導。
  13. To investigate the molecular basis of the stresses - induced gene regulation, the acbadh promoter - / ? - glucuronidase chimeric gene constructs containing six deletions were introduce into tobacco by agrobacterium - mediated transformation

    對啟動子進行6禾缺夫構建，瞬時轉化煙草葉片表明， 6種構建都有活性。
  14. 2. an anther specific chimaeric male sterile gene expression box with a enhanced promoter ( ta29 ) driving coda gene was constructed and the expression box was inserted into binary vector p3301 that contains a l - phosphinothricin ( ppt ) - resistant selective marker gene and - glucuronidase ( gus ) reporter gene in t - dna region

    以增強的ta29啟動子驅動克隆的coda基因，構建成花藥特異性嵌合基因表達盒；將此表達盒插入雙元載體p3301 ，構建成以ppt抗性基因為選擇標記，以gus為報告基因的植物表達載體。
  15. Mature embryo - derived calli of japonica rice ( oryza sativa l. ) cultivars nipponbare were transformed using agrobacterium tumefaciens strain agl1 carrying a binary vector pcas04 harboring the marker gene, neomycin phosphotransferase gene ( nptii ), driven by a promoter from the ubiquitin gene in maize, a promoterless p - glucuronidase gene near to the left border of t - dna for trapping gene and a strong promoter, rice actin - gb promoter, near to the right border of t - dna as activation tagging. in this system, co - cultivation was simplified, special selection stages and pre - regeneration stage were omitted, the whole process was almost under continuous light at 30 ? except co - cultivation and transgenic plants began to generate only after 7 weeks calli were induced

    在一步轉化系統中，光照高溫條件下培養的水稻愈傷組織從誘導開始經過4周時間就可以達到轉化實驗的要求，並且簡化、優化了整個共培養過程，省去了一篩、二篩和預分化步驟，只用7周的時間就可以初步得到再生轉化植株；共191塊愈傷組織得到125塊抗性愈傷組織，轉化頻率達到65 . 4 ，最後共得到99棵獨立來源的再生植株，抗性愈傷組織再生頻率達到79 . 2 。
  16. Furthermore, by inserting " anther box " element to the mutated area of two site - mutation promoters, another two promoters, ipmas and ipmal, were created. in order to study the chemical - inducible capacity of wild and modified pr - la promoters, a coding sequence of gus ( | 3 - glucuronidase ) gene was fused to their downstre am, and the chimeric genes were cloned into pbin ! 9 - based plant expression vector

    為了檢測得到的啟動子驅動效率及誘導活性，將所得到的啟動子、定點突變啟動子和插入花藥盒的啟動子與gus基因連接，構建了6個植物表達載體，同時分別構建包含ipl barnase 、 ipml barnase 、 ipmal barnase嵌合基因的植物表達載體。
分享友人
分享到 Line

分享到臉書