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- W2392372783 abstract "A novel deoxyribonuclease from the fruiting bodies of Ganoderma lucidum has been purified and designated as GLDNase.It was purified by ammonium sulphate precipitation,Blue Sepharose 6 Fast Flow and SP Sepharose Fast Flow.GLDNase showed a single protein band on SDS-PAGE.It showed a major mass peak of 13807 u analyzed in an electrospray-mass analyzer.Amino acid analysis of the N-terminus indicated that the sequence was PLDTGRYHIYTW/T/CDGG.GLDNase acted on both ssDNA and dsDNA.Its optimum pH and temperature were 8.4 and 40 ℃ respectively.It was a kind of non-restriction-endonuclease.Mg2+ was required for the endonuclase activity as a co-factor.The activity of the purified enzyme was completely inhibited by 10 mmol·L-1 EDTA.The oligonucleotides produced by GLDNase had a phosphate group at the 5'-termini and a hydroxyl group at the 3'-termini." @default.
- W2392372783 created "2016-06-24" @default.
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- W2392372783 date "2007-01-01" @default.
- W2392372783 modified "2023-09-23" @default.
- W2392372783 title "Purification and characterization of a novel deoxyriboendonuclease from Ganoderma lucidum" @default.
- W2392372783 hasPublicationYear "2007" @default.
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