L-Rhamnulose 1 -Phosphate Aldolase fromChiut, TehhsingProcedure, ExperimentalHeath, C
Catalog #Pkg SizePriceQuantityShopping Cart R-SG-0161￥ 1 结构式 基本信息产品描述参考文献相关文档 外观粉末或固体 分子量164.16 溶解度N/A CAS号87-96-7 质量控制95.00% 储存条件-20°C in the dark 保存时间1 year 其他信息价格1,就是价格现询 ...
英文名称:L-Rhamnulose 分子式:1 纯度:1% 产地:西安 包装规格:1 品牌:齐岳生物 货号:1 CAS编号:87-96-7 别名:1 cas87-96-7 ;L-Rhamnulose;Einecs 201-785-4;Fucopyranose, L- 英文名称:6-deoxy-L-galactopyranose 中文名称: MF:C6H12O5
This effect is not due to selection of mutants but to enzymic adaptation: induction of D -arabinose isomerase by L -rhamnose has been demonstrated.doi:10.1038/1841315a0FRONTALI, LAURATECCE, GIORGIONature Publishing Group UKNature
l-Rhamnulose 1-phosphate aldolase from Escherichia Coli. II. Characterization as a zinc metalloenzymel-Rhamnulose 1-phosphate aldolase from Escherichia Coli. II. Characterization as a zinc metalloenzymeMetal chelatorsAtomic absorption analysisZincMetallo...
cas:10030-85-0,L-Rhamnulose,L-鼠李糖 化学结构 L-Rhamnulose是一种酮糖,属于脱氧己糖的一种,是L-果糖的6位羟基被氢取代后的产物。 相关研究 酶学研究:L-Rhamnulose激酶和L-Rhamnulose-1-磷酸醛缩酶等酶在L-Rhamnulose的代谢中发挥重要作用,其结构和功能的研究有助于深入理解糖代谢机制。
L-Rhamnulose 1-phosphate aldolase is detected, after removal of nucleoproteins with MnCl2, with a coupled assay system. Two such mutants isolated used in the preparation described are: Rha-58 (kinaseless) and Rha-54 (aldolaseless). They are maintained on nutrient agar slants. The preparation...
(1991). Diastereoselective enzymatic aldol additions: L- rhamnulose and L-fuculose-l-phosphate aldolases from E. coli. Angew. Chem. Int. Ed. Engl. 30, 555-558.Diastereoselective Enzymatic Aldol Additions:L-Rhamnulose and L-Fuculose1-Phosphate Aldolases from E.coli. Fessner,W.D,Sinerius...
The optimal conditions for l-rhamnulose production from l-rhamnose were determined as pH 8.0, 60 °C, 300 g Ll-rhamnose as a substrate, and 0.6 h dilution rate. The half-life of the immobilized enzyme at 60 °C was 809 h. Under the optimal conditions, the immobilized enzyme produced ...
L-Rhamnulose-1-phosphate aldolase from Thermotoga maritima in organic synthesis: One-pot multistep reactions for the preparation of imino- and nitrocyclitols. Adv. Synth. Catal. 2015, 357, 1951-1960. [CrossRef]