Abstract
1. Aminoacyl-transfer-RNA synthetase activity in extracts prepared from tobacco leaf was increased 3–5-fold when sodium thioglycollate (30mm) and magnesium chloride (16mm) were included in the extraction medium. Omitting sucrose (0·45m) from the extraction medium did not alter the activity. 2. Activity was a linear function of enzyme concentration up to 1 disk (30mg. fresh wt.)/ml. and was not affected by dialysis at any concentration. 3. Activity increased about 13-fold above control values when a mixture of 21 amino acids and amides (1mm) was added to the reaction mixture. 4. Under the conditions used in the standard assay for aminoacyl-transfer-RNA synthetase activity Km (ATP) was 0·65mm and Km (l-amino acids) was 70μm. 5. Activity above the control value was found with all amino acids and amides tested except alanine, arginine, glutamic acid, glutamine and hydroxyproline. Activity was highest with leucine, isoleucine, valine, cysteine and histidine. Total activity with a mixture of 21 amino acids and amides was 20% lower than the total activity of the enzymes assayed separately.
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- Allen R. J. The estimation of phosphorus. Biochem J. 1940 Jun;34(6):858–865. doi: 10.1042/bj0340858. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Anderson J. W., Rowan K. S. Activity of aminoacyl-transfer-ribonucleic acid synthetases in tobacco-leaf tissue in relation to senescence and to the action of 6-furfurylaminopurine. Biochem J. 1966 Oct;101(1):15–18. doi: 10.1042/bj1010015. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Anderson J. W., Rowan K. S. Activity of peptidase in tobacco-leaf tissue in relation to senescence. Biochem J. 1965 Dec;97(3):741–746. doi: 10.1042/bj0970741. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Attwood M. M., Cocking E. C. The purification and properties of the alanyl-transfer ribonucleic acid synthetase of tomato roots. Biochem J. 1965 Sep;96(3):616–625. doi: 10.1042/bj0960616. [DOI] [PMC free article] [PubMed] [Google Scholar]
- BOVE J., RAACKE I. D. Amino acid-activating enzymes in isolated chloroplasts from spinach leaves. Arch Biochem Biophys. 1959 Dec;85:521–531. doi: 10.1016/0003-9861(59)90520-x. [DOI] [PubMed] [Google Scholar]
- CLARK J. M., Jr Amino acid activation in plant tissues. J Biol Chem. 1958 Aug;233(2):421–424. [PubMed] [Google Scholar]
- ELLIOTT W. H., COLEMAN G. A method for studying amino acid activation in crude enzyme preparations. Biochim Biophys Acta. 1962 Feb 26;57:236–244. doi: 10.1016/0006-3002(62)91116-2. [DOI] [PubMed] [Google Scholar]
- ELLMAN G. L. The biuret reaction: changes in the ultraviolet absorption spectra and its application to the determination of peptide bonds. Anal Biochem. 1962 Jan;3:40–48. doi: 10.1016/0003-2697(62)90042-8. [DOI] [PubMed] [Google Scholar]
- FRANCKI R. I., BOARDMAN N. K., WILDMAN S. G. PROTEIN SYNTHESIS BY CELL-FREE EXTRACTS FROM TOBACCO LEAVES. I. AMINO ACID INCORPORATING ACTIVITY OF CHLOROPLASTS IN RELATION TO THEIR STRUCTURE. Biochemistry. 1965 May;4:865–872. doi: 10.1021/bi00881a011. [DOI] [PubMed] [Google Scholar]
- FRANCKI R. I., BOARDMAN N. K., WILDMAN S. G. PROTEIN SYNTHESIS BY CELL-FREE EXTRACTS FROM TOBACCO LEAVES. I. AMINO ACID INCORPORATING ACTIVITY OF CHLOROPLASTS IN RELATION TO THEIR STRUCTURE. Biochemistry. 1965 May;4:865–872. doi: 10.1021/bi00881a011. [DOI] [PubMed] [Google Scholar]
- HELE P., FINCH L. R. Amino acid-activating systems from pig liver. Biochem J. 1960 May;75:352–363. doi: 10.1042/bj0750352. [DOI] [PMC free article] [PubMed] [Google Scholar]
- MARCUS A. Amino acid dependent exchange between pyrophosphate and adenosine triphosphate in spinach preparations. J Biol Chem. 1959 May;234(5):1238–1240. [PubMed] [Google Scholar]
- MOUSTAFA E. PURIFICATION AND PROPERTIES OF VALINE-ACTIVATING ENZYME FROM WHEAT GERM. Biochim Biophys Acta. 1963 Oct 15;76:280–285. [PubMed] [Google Scholar]
- NOVELLI G. D. Protein synthesis in microorganisms. Annu Rev Microbiol. 1960;14:65–82. doi: 10.1146/annurev.mi.14.100160.000433. [DOI] [PubMed] [Google Scholar]
- Peterson P. J., Fowden L. Purification, properties and comparative specificities of the enzyme prolyl-transfer ribonucleic acid synthetase from Phaseolus aureus and Polygonatum multiflorum. Biochem J. 1965 Oct;97(1):112–124. doi: 10.1042/bj0970112. [DOI] [PMC free article] [PubMed] [Google Scholar]
- SHAW J. G. ENZYMIC DEGRADATION OF ADENOSINE TRIPHOSPHATE TO ADENINE BY TOBACCO LEAF EXTRACTS, AND ITS RELATIONSHIP TO MEASUREMENTS OF POLYRIBONUCLEOTIDE SYNTHESIS. Arch Biochem Biophys. 1965 Mar;109:627–633. doi: 10.1016/0003-9861(65)90410-8. [DOI] [PubMed] [Google Scholar]
- SPENCER D., WILDMAN S. G. THE INCORPORATION OF AMINO ACIDS INTO PROTEIN BY CELL-FREE EXTRACTS FROM TOBACCO LEAVES. Biochemistry. 1964 Jul;3:954–959. doi: 10.1021/bi00895a019. [DOI] [PubMed] [Google Scholar]
- Spencer D. Protein synthesis by isolated spinach chloroplasts. Arch Biochem Biophys. 1965 Aug;111(2):381–390. doi: 10.1016/0003-9861(65)90200-6. [DOI] [PubMed] [Google Scholar]