Vera J, Alvarez R, Murano E, Slebe JC, Leon O
Instituto de Bioquimica, Facultad de Ciencias, Universidad Austral de Chile, Valdivia, Chile.
Appl Environ Microbiol. 1998 Nov;64(11):4378-83. doi: 10.1128/AEM.64.11.4378-4383.1998.
The phenotypic and agarolytic features of an unidentified marine bacteria that was isolated from the southern Pacific coast was investigated. The strain was gram negative, obligately aerobic, and polarly flagellated. On the basis of several phenotypic characters and a phylogenetic analysis of the genes coding for the 16S rRNA, this strain was identified as Pseudoalteromonas antarctica strain N-1. In solid agar, this isolate produced a diffusible agarase that caused agar softening around the colonies. An extracellular agarase was purified by ammonium sulfate precipitation, gel filtration, and ion-exchange chromatography on DEAE-cellulose. The purified protein was determined to be homogeneous on the basis of sodium dodecyl sulfate-polyacrylamide gel electrophoresis, and it had a molecular mass of 33 kDa. The enzyme hydrolyzed the beta-1,4-glycosydic linkages of agar, yielding neoagarotetraose and neoagarohexaose as the main products, and exhibited maximal activity at pH 7. The enzyme was stable at temperatures up to 30 degreesC, and its activity was not affected by salt concentrations up to 0.5 M NaCl.
对从南太平洋海岸分离出的一种未鉴定海洋细菌的表型和琼脂分解特性进行了研究。该菌株革兰氏阴性,专性需氧,具极生鞭毛。基于几个表型特征以及对编码16S rRNA的基因进行系统发育分析,该菌株被鉴定为南极假交替单胞菌菌株N-1。在固体琼脂中,该分离株产生一种可扩散的琼脂酶,导致菌落周围的琼脂软化。通过硫酸铵沉淀、凝胶过滤和DEAE-纤维素离子交换色谱法纯化了一种胞外琼脂酶。根据十二烷基硫酸钠-聚丙烯酰胺凝胶电泳,纯化后的蛋白质被确定为均一的,其分子量为33 kDa。该酶水解琼脂的β-1,4-糖苷键,产生新琼脂四糖和新琼脂六糖作为主要产物,在pH 7时表现出最大活性。该酶在高达30℃的温度下稳定,其活性不受高达0.5 M NaCl盐浓度的影响。