FIELD: biotechnology.
SUBSTANCE: invention relates to the field of biotechnology and pharmaceutical chemistry. Disclosed is a method of producing a salt α-D-ribofuranose-1-phosphate and salt α-2-D-deoxyribofuranoso-1-phosphate, selected from a barium, magnesium, calcium, sodium or dicyclohexylamine salt. Enzymatic phosphorolysis of 7-methylguanosine hydroiodide salt or 7-methyl-2'-deoxyguanosine hydroiodide salt is performed in the presence of inorganic phosphate or dicyclohexylamine hydrophosphate, and pNP from Enterobacter or E. coli. Obtained α-D-ribofuranose-1-phosphate or α-D-2-deoxyribofuranoso-1-phosphate is reacted with a water-ammonia solution of Ba2+, Mg2+ or Ca2+ acetate to obtain corresponding salt. To obtain sodium salt of dicyclohexylamine salt α-D-ribofuranose-1-phosphate or α-D-2-deoxyribofuranoso-1-phosphate is dissolved in water and ion-exchange resin Dowex-50 in Na+ form is added to solution.
EFFECT: invention provides stereo-specificity of the reaction, complete conversion of the starting compounds and avoids the use of large excess reagents, yield of the desired compounds is 74–96 %.
1 cl, 4 dwg, 10 ex
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Authors
Dates
2019-12-12—Published
2018-08-07—Filed