Abstract
Alginate-entrapped cells of M. pruriens were able to convert a number of parasubstituted monophenolic compounds into the corresponding catechols. All catechols produced were released into the medium, which offered the opportunity to isolate these products via a relatively simple procedure. Prepurification was performed on a Sephadex G10 gel and catechols were concentrated on Affigel 601. The identity of all products was confirmed with combined liquid chromatography/mass spectrometry (LC/MS) or MS using the desorption chemical ionization technique, depending on the catechol. For the entrapped cells and for a cell homogenate prepared of the same cell line ofM. pruriens the substrate specificities were qualitatively identical when judged on initial rates of synthesis calculated on protein basis.
Original language | English |
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Pages (from-to) | 15-26 |
Number of pages | 12 |
Journal | Plant cell tissue and organ culture |
Volume | 13 |
Issue number | 1 |
DOIs | |
Publication status | Published - 1988 |