A6306
琼脂水解酶 来源于大西洋假单胞菌
lyophilized powder, ≥5,000 units/mg protein (Lowry)
别名:
β-琼脂水解酶, 琼脂糖 4-溶菌酶
生物来源
bacterial (Pseudomonas atlantica)
质量水平
表单
lyophilized powder
比活
≥5,000 units/mg protein (Lowry)
储存温度
2-8°C
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外形
产品由磷酸盐缓冲盐、牛血清白蛋白和琼胶酶配制而成。 总蛋白质含量范围在10 – 30% w/w之间。
其他说明
一个单位将在40°C 、 pH 6.0 下每分钟从琼脂产生 1.0μg 还原糖（以 D -半乳糖测量）。
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
法规信息
常规特殊物品
此项目有
历史批次信息供参考:
分析证书(COA)
Lot/Batch Number
Chulhong Oh et al.
Journal of bacteriology, 193(19), 5538-5538 (2011-09-15)
We report here the annotated genome sequence of the marine bacterium Alteromonas sp. S89 and the identification of six genes coding for agar-degrading enzymes. The sequenced Alteromonas sp. S89 genome is composed of a 3,864,871-bp circular chromosome that includes 3,236
Li Liao et al.
Applied and environmental microbiology, 77(19), 7077-7079 (2011-08-09)
A new agarase, AgaA(CN41), cloned from Vibrio sp. strain CN41, consists of 990 amino acids, with only 49% amino acid sequence identity with known β-agarases. AgaA(CN41) belongs to the GH50 (glycoside hydrolase 50) family but yields neoagarotetraose as the end
Aiming Ren et al.
Acta crystallographica. Section F, Structural biology and crystallization communications, 66(Pt 12), 1635-1639 (2010-12-09)
AgaB from Pseudoalteromonas sp. CY24 is a novel agarase that hydrolyzes agarose to generate products with inverted anomeric configuration and that has been proposed to have a larger catalytic cleft than other β-agarases. Here, the expression, purification, crystallization and data
Young Hoon Oh et al.
Journal of microbiology and biotechnology, 21(8), 818-821 (2011-08-31)
An agar-degrading bacterium was isolated from the guts of spiny turban shells. It was identified as a Pseudoalteromonas species and named Pseudoalteromonas sp. JYBCL 1. The viscosity of the inoculated agar medium decreased by more than 60% after 20 h
Michael-Paul Vockenhuber et al.
Microbiology (Reading, England), 158(Pt 2), 424-435 (2011-11-15)
Transcriptional regulation of primary and secondary metabolism is well-studied in Streptomyces coelicolor, a model organism for antibiotic production and cell differentiation. In contrast, little is known about post-transcriptional regulation and the potential functions of small non-coding RNAs (sRNAs) in this
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