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一般描述
尿苷-5′-二磷酸葡萄糖焦磷酸化酶(UDP-glc-PPase)普遍存在于植物、酵母、细菌和哺乳动物中。这种酶是由八个相同亚基组成的八聚体。
应用
来自面包酵母的尿苷-5′-二磷酸葡萄糖焦磷酸化酶′已用于:
- 合成尿苷-5′-二磷酸葡萄糖(UDP-Glc)-13C9
- 量化水稻中蔗糖合酶(SUS)的活性
- 研究己糖激酶和糖原合成酶控制青蛙卵母细胞通量的作用
生化/生理作用
尿苷-5′-二磷酸葡萄糖焦磷酸化酶(UDP-glc-PPase)参与催化UDP-葡萄糖的合成。这种酶的活性需要二价阳离子,例如Mg2+、Ca2+、Mn2+、Ni2+。
单位定义
一个单位将在25℃和pH 7.6下,每分钟由尿苷-5′-二磷酸葡萄糖和无机焦磷酸盐形成1.0 μmole的1-磷酸葡萄糖。
外形
冻干粉,不含硫酸盐,含柠檬酸缓冲盐
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
法规信息
常规特殊物品
从最新的版本中选择一种:
Clinica chimica acta; international journal of clinical chemistry, 86(3), 329-332 (1978-06-15)
The concentration of pyrophosphate in urine has been determined using the enzyme uridine-5'-diphosphoglucose pyrophosphorylase. The technique is relatively quick and easy to perform. Reproducibility of results was good, and results from recovery experiments were excellent. The mean concentration of pyrophosphate
Molecular biology reports, 38(4), 2751-2760 (2010-11-26)
UDP-Glucose Pyrophosphorylase (EC 2.7.7.9, UGPase) plays an important role in Streptococcus equi subsp. zooepidemicus (S. zooepidemicus) cell envelope Hyaluronic acid (HA) biosynthesis and it is also recognized as a virulence determinant in several bacterial species. HA is valuable biopolymer used
Microbial drug resistance (Larchmont, N.Y.), 17(1), 75-81 (2010-12-07)
Prevalence of serotype 6B penicillin (PEN)-nonsusceptible Streptococcus pneumoniae significantly increased from 15.8% (1993-1997) to 67.3% (1998-2002) (p<0.001) in Argentina. Serogroup 6 ranks fourth among different capsular types within invasive isolates from Argentinean patients <6 years of age. To evaluate whether
Methods in enzymology, 500, 355-370 (2011-09-29)
In this chapter, we describe the steps needed to create a kinetic model of a metabolic pathway based on kinetic data from experimental measurements and literature review. Our methodology is presented by utilizing the example of trehalose metabolism in yeast.
Journal of biotechnology, 154(4), 212-215 (2011-06-15)
UDP-sugars are widely used as substrates in the synthesis of oligosaccharides catalyzed by glycosyltransferases. In the present work a metabolic engineering strategy aimed to direct the carbon flux towards UDP-glucose and UDP-galactose biosynthesis was successfully applied in Lactobacillus casei. The
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