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Characterization of the Pseudomonas aeruginosa alginate lyase gene (algL): cloning, sequencing, and expression in Escherichia coli.

机译:铜绿假单胞菌藻酸盐裂解酶基因(algL)的表征:大肠杆菌中的克隆,测序和表达。

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摘要

Mucoid strains of Pseudomonas aeruginosa produce a viscous exopolysaccharide called alginate and also express alginate lyase activity which can degrade this polymer. By transposon mutagenesis and gene replacement techniques, the algL gene encoding a P. aeruginosa alginate lyase enzyme was found to reside between algG and algA within the alginate biosynthetic gene cluster at 35 min on the P. aeruginosa chromosome. DNA sequencing data for algL predicted a protein product of ca. 41 kDa, including a 27-amino-acid signal sequence, which would be consistent with its possible localization in the periplasmic space. Expression of the algL gene in Escherichia coli cells resulted in the expression of alginate lyase activity and the appearance of a new protein of ca. 39 kDa detected on sodium dodecyl sulfate-polyacrylamide gels. In mucoid P. aeruginosa strains, expression of algL was regulated by AlgB, which also controls expression of other genes within the alginate gene cluster. Since alginate lyase activity is associated with the ability to produce and secrete alginate polymers, alginate lyase may play a role in alginate production.
机译:铜绿假单胞菌的粘液状菌株产生称为藻酸盐的粘性胞外多糖,并且还表达可以降解该聚合物的藻酸盐裂合酶活性。通过转座子诱变和基因替换技术,发现铜绿假单胞菌藻酸盐裂解酶的algL基因在35分钟的铜绿假单胞菌染色体上位于藻酸盐生物合成基因簇内的algG和algA之间。针对algL的DNA测序数据预测了约一个蛋白质产物。 41 kDa,包括27个氨基酸的信号序列,与其在周质空间中的可能定位一致。 algL基因在大肠杆菌细胞中的表达导致藻酸裂解酶活性的表达和新的ca蛋白的出现。在十二烷基硫酸钠-聚丙烯酰胺凝胶上检测到39 kDa。在黏液状铜绿假单胞菌菌株中,algL的表达受AlgB调节,AlgB也控制藻酸盐基因簇中其他基因的表达。由于藻酸盐裂解酶活性与产生和分泌藻酸盐聚合物的能力有关,因此藻酸盐裂解酶可能在藻酸盐生产中起作用。

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