
In order to improve the production of the cytotoxic lignan podophyllotoxin, seven precursors from the phenylpropanoid-routing and one related compound were fed to cell suspension cultures derived from the rhizomes of Podophyllum hexandrum Royle. These cell cultures were able to convert only coniferin into podophyllotoxin, maximally a 12.8 fold increase in content was found. Permeabilization using isopropanol, in combination with coniferin as a substrate, did not result in an extra increase in podophyllotoxin accumulation. Concentrations of isopropanol exceeding 0.5% (v/v) were found to be rather toxic for suspension growth cells of P. hexandrum. When coniferin was fed in presence of such isopropanol concentrations, beta-glucosidase activity was still present, resulting in the formation of the aglucon coniferyl alcohol. In addition, podophyllotoxin was released into the medium under these permeabilization conditions. Entrapment of P. hexandrum cells in calcium-alginate as such or in combination with the feeding of biosynthetic precursors, did not improve the podophyllotoxin production. Cell-free medium from suspension cultures at later growth stages incubated with coniferin, resulted in the synthesis of the lignan pinoresinol.
BIOCONVERSION, PODOPHYLLOTOXIN, PODOPHYLLUM-HEXANDRUM, CONIFERIN, L-DOPA, ALGINATE-ENTRAPPED CELLS, PERMEABILIZATION, PHENYLPROPANOID PRECURSORS, LIGNAN BIOSYNTHESIS, MUCUNA-PRURIENS, LIGNANS, ETOPOSIDE, BIOSYNTHESIS, PELTATUM
BIOCONVERSION, PODOPHYLLOTOXIN, PODOPHYLLUM-HEXANDRUM, CONIFERIN, L-DOPA, ALGINATE-ENTRAPPED CELLS, PERMEABILIZATION, PHENYLPROPANOID PRECURSORS, LIGNAN BIOSYNTHESIS, MUCUNA-PRURIENS, LIGNANS, ETOPOSIDE, BIOSYNTHESIS, PELTATUM
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