Transfer RNA-dependent amino acid biosynthesis:: An essential route to asparagine formation

被引:79
作者
Min, B
Pelaschier, JT
Graham, DE
Tumbula-Hansen, D
Söll, D
机构
[1] Yale Univ, Dept Mol Biophys & Biochem, New Haven, CT 06520 USA
[2] Yale Univ, Dept Chem, New Haven, CT 06520 USA
[3] Virginia Polytech Inst & State Univ, Dept Biochem, Blacksburg, VA 24061 USA
关键词
D O I
10.1073/pnas.012027399
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Biochemical experiments and genomic sequence analysis showed that Deinococcus radiodurans and Thermus thermophilus do not possess asparagine synthetase (encoded by asnA or asnB), the enzyme forming asparagine from aspartate. Instead these organisms derive asparagine from asparaginyl-tRNA, which is made from aspartate in the tRNA-dependent transamidation pathway [Becker, H. D. & Kern, D. (1998) Proc. Natl. Acad. Sci. USA 95, 12832-12837; and Curnow, A. W., Tumbula, D. L., Pelaschier, J. T., Min, B. & 5611, D. (1998) Proc. Natl. Acad. Sci. USA 95, 12838-12843]. A genetic knockout disrupting this pathway deprives D. radiodurans of the ability to synthesize asparagine and confers asparagine auxotrophy. The organism's capacity to make asparagine could be restored by transformation with Escherichia coli asnB. This result demonstrates that in Deinococcus, the only route to asparagine is via asparaginyl-tRNA. Analysis of the completed genomes of many bacteria reveal that, barring the existence of an unknown pathway of asparagine biosynthesis, a wide spectrum of bacteria rely on the tRNA-dependent transamidation pathway as the sole route to asparagine.
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页码:2678 / 2683
页数:6
相关论文
共 40 条
[1]  
ADACHI J, 1996, COMPUT SCI MONOGR, V28, P1
[2]   Thermus thermophilus contains an eubacterial and an archaebacterial aspartyl-tRNA synthetase [J].
Becker, HD ;
Roy, H ;
Moulinier, L ;
Mazauric, MH ;
Keith, G ;
Kern, D .
BIOCHEMISTRY, 2000, 39 (12) :3216-3230
[3]   Existence of two distinct aspartyl-tRNA synthetases in Thermus thermophilus. Structural and biochemical properties of the two enzymes [J].
Becker, HD ;
Reinbolt, J ;
Kreutzer, R ;
Giege, R ;
Kern, D .
BIOCHEMISTRY, 1997, 36 (29) :8785-8797
[4]   Thermus thermophilus:: A link in evolution of the tRNA-dependent amino acid amidation pathways [J].
Becker, HD ;
Kern, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (22) :12832-12837
[5]   The many routes of bacterial transfer RNAs after aminoacylation [J].
Blanquet, S ;
Mechulam, Y ;
Schmitt, E .
CURRENT OPINION IN STRUCTURAL BIOLOGY, 2000, 10 (01) :95-101
[6]  
Bock A, 2000, Biofactors, V11, P77
[7]  
CEDAR H, 1969, J BIOL CHEM, V244, P4122
[8]   Glutamyl-tRNAGln amidotransferase in Deinococcus radiodurans may be confined to asparagine biosynthesis [J].
Curnow, AW ;
Tumbula, DL ;
Pelaschier, JT ;
Min, B ;
Söll, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (22) :12838-12843
[9]   IN-VIVO DAMAGE AND RECA-DEPENDENT REPAIR OF PLASMID AND CHROMOSOMAL DNA IN THE RADIATION-RESISTANT BACTERIUM DEINOCOCCUS RADIODURANS [J].
DALY, MJ ;
LING, OY ;
FUCHS, P ;
MINTON, KW .
JOURNAL OF BACTERIOLOGY, 1994, 176 (12) :3508-3517
[10]   FACTORS DETERMINING SPECIFICITY OF TERTIARY RNA AMINOACYLATION REACTION - NON-ABSOLUTE SPECIFICITY OF TERTIARY RNA-AMINOACYL TERTIARY RNA-SYNTHETASE RECOGNITION AND PARTICULAR IMPORTANCE OF MAXIMAL VELOCITY [J].
EBEL, JP ;
GIEGE, R ;
BONNET, J ;
KERN, D ;
BEFORT, N ;
BOLLACK, C ;
FASIOLO, F ;
GANGLOFF, J ;
DIRHEIMER, G .
BIOCHIMIE, 1973, 55 (05) :547-557