Separation of cell wall associated enzyme solution of sour cherry (Prunus cerasus L.)
Kovacs E.; Nemeth-Szerdahelyi E. and Horvath S.
5th International Postharvest Symposium . Volume of Abstract . Verona, Italy 6-11 June 2004. p 97.
2004
บทคัดย่อ
Different sour cherry cultivars (…rdi bitermi Kantorjanosi, Pandy 279) were investigated at harvest. Enzyme solution was prepared by Kavacs et.al. (1997). SDS-PAGE was performed using a mini gel system (Mini-Protean II Dual Slab, Bio-Rad). The protein bands were evaluated by a Biotec Fisher video densitometer. For identification b-galactosidase from Saccharomyces fragilis (EC 3.2.1 23, Sigma) and molecular mass markers (Pharmacia) were used. Electrophoresis and Protein blotting was used for identification of b-galactosidase were used according to Kovacs and Nemeth-Szerdahelyi (2002). The total protein content was determined according to the method of
The main observations were: the activities of b-galactosidase were different among cultivars; the enzyme consisted of different protein bands (16 kDa, 22 kDa, 50 kDa) separating by SDS-PAGE. The isoelectric focusing pattern of the crude enzyme solution showed differences of cultivars (Pandy 279 has less protein bands, than the others).