On the Nucleic Acids of Microbial Origin Separated by Use of Continuous Paper Electrophoresis

Akashi, Shuzo; Yokoi, Hanako

doi:10.1093/oxfordjournals.jbchem.a126826

Cited by 4 publications

(2 citation statements)

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“…The pmr spectra of 5 '-A-(L-phenylalanyl)-5 '-amino-2',5'-dideoxyadenosine (4b) has been compared to a spectra of a mixture of 5'-amino-2',5'-dideoxyadenosine (1) and L-phenylalanine (Table II). The 0.15-0.3-ppm high-field shifts in 4b compare closely with the 0.1-0.25ppm shifts found for the comparisons of ApA vs. the mixture of 5 '-AMP and 3 '-AMP.36 These data provide evidence for phenyl and adenine ring stacking.…”

Section: Additionsmentioning

confidence: 99%

Nucleoside peptides. I. Synthesis of 5'-deoxy-5'amino-5'-N-aminoacyl peptide derivatives of guanosine, adenosine, and 2'-deoxyadenosine and their effect of cell-free protein synthesis

Robins¹,

Simon²,

Stout³

et al. 1971

J. Am. Chem. Soc.

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Several 5'-A-aminoacyl-5'-amino-5 '-deoxy-and 5'-amino-2',5 '-dideoxy-9-/3-D-ribofuranosylpurine nucleoside peptides have been synthesized which represent a new class of peptide nucleosides. Appropriately blocked amino acids and peptides have been coupled to the corresponding purine 5 '-amino-5 '-deoxynucleoside derivative by the active ester and DCC methods of peptide formation. These compounds have been studied to determine their effect on poly-U directed polyphenylalanine synthesis. In instances where the aminoacyl moiety was L-phenylalanine and the nucleoside was either 5 '-amino-5 '-deoxyadenosine or 5 '-amino-2 ',5 '-dideoxyadenosine,

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Section: Additionsmentioning

confidence: 99%

Nucleoside peptides. I. Synthesis of 5'-deoxy-5'amino-5'-N-aminoacyl peptide derivatives of guanosine, adenosine, and 2'-deoxyadenosine and their effect of cell-free protein synthesis

Robins¹,

Simon²,

Stout³

et al. 1971

J. Am. Chem. Soc.

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“…S-Adenosylmethionine, the cofactor responsible for methylation, is one example, as are a wide variety of nucleoside antibiotics (Suhadolnik, 1970). Amino acids were first shown to bind covalently to RNA in 1958 (Akashi & Yokoi, 1958). Covalent * Author to whom all correspondence should be addressed.…”

mentioning

confidence: 99%

Structure of N-[1'(9-adenyl)-β-D-ribofuranuronosyl]-L-phenylalanine water ethanol (1/0.5/0.25), C19H20N6O6.0.5H2O.0.25C2H6O

Takusagawa¹,

Berman²,

Dabrow³

et al. 1985

Acta Crystallogr C

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Abstract. M r = 448.94, monoclinic, P21, a = 9.207 (1), b= 10.503 (2), c= 22.208 (3),/k, fl= 101.4 (1) °, V = 2105.2 (9) •3, Z = 4, D x = 1.416 gcm -3, 2(Cu Ka) = 1-5418 A, ~t = 9.3 cm -1, F(000) = 942, T= 293 K. Final R =0.053 for 4132 observed intensities. Both independent molecules in the asymmetric unit are zwitterions. One molecule has an extended conformation with the base anti and the sugar C(2') endo (2E); the other molecule has a closed conformation with the base syn and the sugar C(3') endo (3E).

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Inaktivierung des Salmonella-Bakteriophagen P 22 durch Chloroform

Prell

1960

Archiv. Mikrobiol.

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On the Nucleic Acids of Microbial Origin Separated by Use of Continuous Paper Electrophoresis

Cited by 4 publications

References 0 publications

Nucleoside peptides. I. Synthesis of 5'-deoxy-5'amino-5'-N-aminoacyl peptide derivatives of guanosine, adenosine, and 2'-deoxyadenosine and their effect of cell-free protein synthesis

Nucleoside peptides. I. Synthesis of 5'-deoxy-5'amino-5'-N-aminoacyl peptide derivatives of guanosine, adenosine, and 2'-deoxyadenosine and their effect of cell-free protein synthesis

Structure of N-[1'(9-adenyl)-β-D-ribofuranuronosyl]-L-phenylalanine water ethanol (1/0.5/0.25), C19H20N6O6.0.5H2O.0.25C2H6O

Inaktivierung des Salmonella-Bakteriophagen P 22 durch Chloroform

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