Isoprenylation of transfer ribonucleic acid

A two-fold difference in the total N⁶-(Δ²-isopentenyl) adenosine content was found between the serine accepting tRNA fractions from adult and embryonic bovine liver. Elution profiles of benzoylated DEAE cellulose showed three peaks of adult tRNA were capable of accepting serine. Using gas-liquid chromatography, each peak had measurable amounts of N⁶-(Δ²-isopentenyl) adenosine. When the same techniques were applied to embryonic bovine tRNA, three peaks accepted serine; however, only one peak contained N⁶-(Δ²-isopentenyl) adenosine. These results can be interpreted to indicate that adult and embryonic tRNA differ in the N⁶-(Δ²-isopentenyl) adenosine content of tRNA^ser.     

Crystallization of transfer ribonucleic acids

A compilation of crystallization experiments of tRNAs published in literature as well as original results are given and discussed in this paper. Up to now 17 different tRNA species originating from Escherichia coli and from the yeast Saccharomyces cerevisiae have been crystallized. All structural tRNA families are represented, namely the tRNAs with large or small extra-loops and among them the initiator tRNAs. The tRNAs with small variable loops (4 to 5 nucleotides), e.g. tRNAAsp and tRNAPhe, yield the best diffracting crystals. Crystalline polymorphism is a common feature; about 100 different crystal forms have been observed, but only 6 among them enabled structure determination studies by X-ray diffraction. Crystallization strongly depends upon experimental parameters such as the presence of polyamines and magnesium as well as upon the purity and the molecular integrity of the tRNAs. Crystals are usually obtained by vapour diffusion methods using salts (e.g. ammonium sulfate), organic solvents (e.g. isopropanol, dioxane or 2-methyl-2,4-pentane diol) or polyethylene glycol as precipitants. A methodological strategy for crystallyzing new tRNA species is described.