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glucosidase造句

"glucosidase"是什么意思  
造句与例句手机版
  • Study on - glucosidase inhibitors in morus alba
    葡萄糖苷酶抑制作用研究
  • Inhibition of polygonum multiflorum thunb on - glucosidase activity
    葡萄糖苷酶活性的抑制作用
  • Purification and properties of - glucosidase from chaetomium thermophilum
    葡萄糖苷酶的分离纯化及特性
  • Screening for - glucosidase inhibitors from extracts of traditional chinese medicine
    葡萄糖苷酶抑制剂的筛选
  • The expression of oligo - 1 , 6 - glucosidase from bacillus subtilis in pichia pastoris
    基因在毕赤酵母中的表达及酶学性质研究
  • W - 20 dentified as aspergillus sp . , has high a - glucosidase inhibitory activity
    124mg ml ,显示了相当高的a葡萄糖f酶抑制活性。
  • P - glucosidase ( - glc ) take a very important function to tea aroma and stress
    -葡萄糖苷酶在茶叶香气和抗逆性方面有着举足轻重的作用。
  • Methods for the inspection of escherichia coli in food for export . fluorescence measurement of glucosidase
    出口食品中大肠杆菌葡萄糖苷酶荧光检验方法
  • Relationship of seminal fructose concentration , activity of neutral alpha - glucosidase , acid phosphatase with semen parameters
    糖苷酶和酸性磷酸酶活性与精液参数关系研究
  • Ganodermataceae is a new , important resource for antimicrobial , antitumor and a - glucosidase inhibitory agents
    灵芝真菌是重要的抗菌、抗肿瘤和-葡萄糖苷酶抑制剂的新菌源。
  • It's difficult to see glucosidase in a sentence. 用glucosidase造句挺难的
  • The alpha - glucosidase breaks down carbohydrates into glucose molecules which are then absorbed into the blood stream
    阿尔法-葡萄糖苷酶可以将碳水化合物分解成葡萄糖,葡萄糖会被吸收到血液中去。
  • The anti - diabetic drug miglitol , an alpha - glucosidase inhibitor , was the first choice for the therapy of type ii diabetes
    摘要米格列醇作?一种新型-葡糖苷酶抑制剂,能够有效治疗型糖尿病, ?已迅速成?首选药物。
  • Continue metformin . additionally continue sulfonylureas when starting basal insulin therapy . - glucosidase inhibitors may also be continued
    继续应用二甲双胍。开始应用基础胰岛素治疗时还可以继续应用磺脲类药物。 -糖苷酶抑制剂也可以继续使用。
  • Pycnogenol ? was shown to inhibit the intestinal enzymes ( alpha - glucosidase ) involved in the digestion of complex carbohydrates such as starch and normal table sugar
    碧萝芷?可以抑制肠道内的负责如淀粉和白糖等复合碳水化合物的消化的酶(阿尔法-葡萄糖苷酶)的活动能力。
  • The activity of crude enzyme prepared from the jasmine flower enlarged at 23 : 00 and lowed at the late stage . 3 - glucosidase activity rose slightly at 2 0 : 00 . this suggested that p - glucosidase participated in the aroma releasing
    酯酶同工酶中rf值为0 . 325的酶可能与开放释香成负相关性,而rf值为0 . 83的酶可能参与了茉莉花的开放释香。
  • 854 % macrofungi have a - glucosidase inhibitory activity and belong to polyporaceae , ganodermataceae and sclerodermataceae , and 71 . 4 % of which have high bioactivity ( inhibitory percentage > 65 % ) . their activitise are as good as acarbose ' s
    4的种具有较高的生物活性,菌体提取液( 5ml g )的生物活性接近甚至超过拜糖平25mg ml时的抑制水平。
  • Ganoderma sp . 24 , ganoderma australe ( fr . ) pat . 60 and ganoderma sanmingense zhao et zhang 63 show high activities of inhibiting kb or hl - 60 cells , and ganoderma sp . 24 and ganoderma sanmingense zhao et zhang 63 have a - glucosidase inhibitory activities in vitro
    树舌24和南方树舌60的氯仿相对kb细胞和hl - 60细胞摘要都有抑制活性:而三明树舌63 “的乙酸乙酯相对b细胞有一定的抑制活性。
  • In the study , four models were applied and used for prescreening antimicrobial , antitumor and the a - glucosidase inhibitory agents from medicinal fungi including filamentous fungi and macro fungi in fujian ; we studied the antimicrobial , antitumor and a - glucosidase inhibitory activities of three kinds of ganoderma sp . ; as well as we studied the a - glucosidase inhibitor from filamentous fungi w - 20 and its physical and chemical properties . there are abundant antimicrobial , antitumor and a - glucosidase inhibitory agents in filamentous fungi and macrofungi
    本课题以福建省的药用真菌资源为对象,应用了抗菌、抗肿瘤和-葡萄糖苷酶抑制剂的体外筛选模型,进行了药(食)用曲的丝状真菌和大型真菌生物活性物质的筛选;对3种灵芝真菌的抗菌抗肿瘤、 -葡萄糖苷酶抑制活性,以及丝状真菌w - 20抑制-葡萄糖苷酶的活性物质及其理化性质进行了初步研究,为我省药用资源的开发利用打基础。
  • 3 . 2 . 1 . 4 ) which was prepared by precipitation of the water extract of the culture of aspergillus niger with ammonium sulfate and desalted by sephadex g - 25 , and was further fractionated by two steps of deae - toyopearl 650m and one step of poros 20pi chromatography . the other was a p - glucosidase ( ec . 3 . 2 . 1 . 21 ) which was prepared by the above g - 25 fractions and was further fractionated by two steps of deae - toyopearl 650m chromatography . the specific activity of the endoglucanase with sodium carboxymethyl cellulose was estimated to be 433 . 38 hj / mg
    -葡萄糖苷酶对水杨素的比活力为597 . 12iu mg ,并对其专一,不能水解棉花和羧甲基纤维素钠;分子量为117 . 5kda ,加dtt后分子量不变;该组分最适ph和温度分别为4 . 5和70 ,在ph5 . 0 、 50下对水杨素钠的米氏常数km为3 . 73mg ml ,最大反应速度vm为0 . 088mg葡萄糖( ml ? min ) ;与文献中从黑曲霉中分离的-葡萄糖苷酶比较后发现,该组分是一个新的-葡萄糖苷酶。
  • Its km for sacilin at50 andph5 . owas3 . 73mg / ml . with the analysis of kinetics , the p - glucosidase showed synergistic action to the endoglucanase and the endoglucanase inhibited the p - glucosidase . the mechanism for their interaction was explained that the endoglucanase was combined with its products and the inhibition of these products to endoglucanase was removed by its hydrolysis by p - glucosidase
    经两组分共同作用的酶反应动力学分析后发现,两组分这种相互作用机制的核心是:内切酶和?葡萄糖苷酶与内切酶的水解产物,也是其底物类似物? ?纤维二糖和纤维寡糖的结合以及-葡萄糖苷酶对该产物的水解。
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