Abstract
Zein, a corn protein, is a mixture of the polypeptides α-, γ-, β-, and δ-zein. α-Zein and γ-zein comprise 70–85% and 10–20% of total zein mass, respectively. Both peptides have similar amino acid composition, except γ-zein is rich in cysteine. The presence of cysteine has been associated with gelation of zein solutions. A common solvent for zein is aqueous ethanol. Preliminary results suggested that pH and ethanol content affect the rheology of zein solutions. Our objective was to investigate the effect of ethanol content (65–90%) and pH of the solvent (2, 6, and 12) on rheological properties of zein solutions (20% w/w) containing γ-zein. Steady shear tests and oscillatory time sweeps were performed to determine flow behavior and gelation time of zein solutions. Results indicated that α-zein solutions were nearly Newtonian while those containing γ-zein showed shear thinning behavior. At high pH, γ-zein increased the consistency index (K) and shortened gelation time. Results were attributed to the cysteine in γ-zein. High pH promoted formation of disulfide bonds leading to higher K values and shorter gelation times. Results of this work are expected to be useful in the design of zein extraction processes and the development of new zein applications.
Published Version
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