Cloning, heterologous expression, and enzymatic characterization of a novel glucoamylase GlucaM from Corallococcus sp. strain EGB
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GlucaM shared no significant similarity with these glucoamylases (<10% identity), indicating that GlucaM may be a novel glucoamylase.

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The activity of GlucaM was independent of Ca2+.

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GlucaM is also highly resistant to high salt concentrations and various detergents.

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rGlucaM could act on different substrates and maltooligosaccharides, making it a good catalyst for production of glucose

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