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Directory UMM :Data Elmu:jurnal:P:PlantScience:PlantScience_Elsevier:Vol157.Issue2.2000:

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Table 188 kDa Debranching enzyme purification
Fig. 1. Purification of Chlamydomonas debranching enzymes.A. 400 mg of crude protein was loaded on a S-300 HR (1cm) gel filtration FPLC
Fig. 3. Hydrogen peroxide inhibition of ChlamydomonasDBEs 5 mg of either pullulan or glycogen were digested withpeak fraction volumes were used) of fraction containing,respectively the 95 kDa limit dextrinase (the anion exchange (Table 2) and the semi-pure
Fig. 4. Substrate specificity of debranching enzymes. A. 5 mg of substrate polysaccharide were digested with 50 �l of fractioncontaining the semi-pure 88 kDa polypeptide-containing DBE complex of Chlamydomonas (fraction 19–20 from the anionexchange (Table 1
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