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Search Purification (Commentary)

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Results 1 - 8 of 8
EC Number Purification (Commentary) Reference
Display the word mapDisplay the reaction diagram Show all sequences 3.4.22.14- 684521, 752807
Display the word mapDisplay the reaction diagram Show all sequences 3.4.22.14Act d 1 is purified from kiwifruit extracts by covalent chromatography using activated thiopropyl sepharose 6B 700290
Display the word mapDisplay the reaction diagram Show all sequences 3.4.22.14actinidin can be separated into six proteases, named KP1, KP2, KP3, KP4, KP5 and KP6 81474
Display the word mapDisplay the reaction diagram Show all sequences 3.4.22.14Actinidin is purified from the soluble fraction of kiwi fruit by ion exchange chromatography on DE-52 and Mono-Q columns 698404
Display the word mapDisplay the reaction diagram Show all sequences 3.4.22.14ammonium sulfate precipitation and DEAE-Sephadex gel filtration 709327
Display the word mapDisplay the reaction diagram Show all sequences 3.4.22.14DEAE-Sephadex A-50 gel filtration and SP-Sephadex C-50 gel filtration 717622, 718203
Display the word mapDisplay the reaction diagram Show all sequences 3.4.22.14multiple forms 81492
Display the word mapDisplay the reaction diagram Show all sequences 3.4.22.14the enzyme fraction is precipitated from kiwifruit extract by 60% saturation of ammonium sulfate. The precipitate is redissolved in 50 mM citrate buffer (pH 5.5) and dialyzed overnight against this buffer. The dialyzate is loaded into a DEAE-Sepharose Fast Flow column, which pre-equilibrated with the same buffer. The adsorbed fractions are eluted with 0.0-1 M linear gradient of sodium chloride in the buffer 684521
Results 1 - 8 of 8