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Studies on deoxyribonucleic acids and related compounds. V. Synthesis of pentadecanucleotide duplex containing the ideal Pribnow sequence of promoter by the phosphotriester method using a new phosphorylating reagent
Author(s) -
Eiko Ohtsuka,
Yoshio Taniyama,
Ryuji Marumoto,
Hiroko Sato,
Haruhisa Hirosaki,
Morio Ikehara
Publication year - 1982
Publication title -
nucleic acids research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/10.8.2597
Subject(s) - oligonucleotide , reagent , duplex (building) , biology , sequence (biology) , nucleotide , phosphorylation , oligonucleotide synthesis , dna , combinatorial chemistry , ideal (ethics) , nucleic acid sequence , biochemistry , stereochemistry , organic chemistry , chemistry , gene , philosophy , epistemology
A phosphorylating reagent o-chlorophenyl phosphoro-p-anisi-dochloridate was synthesized to phosphorylate the 3'-hydroxyl group of N, 5'-protected deoxynucleosides. These nucleotides served as 3'-terminal units for the synthesis of oligonucleotide blocks. By condensation of these oligonucleotide blocks the partially complementary deoxypentadecanucleotides dAGCTTATAATGC-TCG and dAGCTCGAGCATTATA, which contained the ideal Pribnow sequence TATAATG, were synthesized.

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