Molecular Cloning and Optimization for High Level Expression of Cold-Adapted Serine Protease from Antarctic Yeast <i>Glaciozyma antarctica</i> PI12

<table>(a) Casein hydrolysis on skim milk agar plate. (b) Negative staining with enlargement of 10,000x, bar = 2 <i>μ</i>m. (c) Simple staining photograph. (d) Scanning electron microscopy (SEM) photograph with magnification 2500x. Bar = 10 <i>μ</i>m.</table>

Enzyme Research

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Figure 1

Figure 1: Molecular Cloning and Optimization for High Level Expression of Cold-Adapted Serine Protease from Antarctic Yeast <i>Glaciozyma antarctica</i> PI12 

Figure 1 | Molecular Cloning and Optimization for High Level Expression of Cold-Adapted Serine Protease from Antarctic Yeast Glaciozyma antarctica PI12 