Isolation and amino acid sequence of the 30S ribosomal protein S19 from Mycobacterium bovis BCG

FEBS Letters

Kimura, Makoto²  Yamada, Takeshi¹  Higashi, Yoshinori²  Ohara, Naoya¹ 

[1] Nagasaki University, School of Dentistry, 1-7-1 Sakamoto-machi, Nagasaki 852, Japan;Laboratory of Biochemistry, Faculty of Agriculture, Kyushu University, Fukuoka 812, Japan

关键词: Mycobacterium bovis BCG;    Ribosomal protein;    Amino acid sequence;    MboS19;    Mycobacterium bovis BCG ribosomal protein S19;    EcoS19;    Escherichia coli ribosomal protein S19;    BstS19;    Bacillus stearothermophilus ribosomal protein S19;    RP-HPLC;    reverse phase-high performance liquid chromatography;    TFA;    trifluoroacetic acid;    PVDF;    polyvinylidendifluoride;   

DOI  :  10.1016/0014-5793(93)80287-5

学科分类：生物化学/生物物理

来源: John Wiley & Sons Ltd.

【 摘 要 】

The 30S ribosomal proteins from Mycobacterium bovis BCG were separated by reverse phase-high performance liquid chromatography (RP-HPLC). The isolated proteins were analyzed by SDS-PAGE, blotted on PVDF-membranes and subjected to sequence analyses using a gas-phase sequencer to correlate them to those of the well studied Escherichia coli and Bacillus stearothermophilus ribosomes. Moreover, the internal amino acid sequence of one ribosomal protein, MboS19, which is homologous to E. coli ribosomal protein S19 (EcoS19) and B. stearothermophilus ribosomal protein S19 (BstS19), was further analyzed by sequencing its internal peptides and two segments from the N- and C-termini of the protein were selected to deduce the sequence of two oligonucleotide primers which were used in a polymerase chain reaction. Using the amplified DNA fragment thus obtained as a hybridization probe, the gene encoding protein S19 was identified and cloned. Sequence analysis of the DNA fragment, together with peptide sequence analysis could determine the complete amino acid sequence of MboS19. This sequence proved to be 64% and 71% identical to those of the corresponding S19 proteins from the eubacteria E. coli, and B. stearothermophilus, respectively; 33% of the residues of MboS19 were identical to those in the archaebacteral ribosomal protein HmaS19.

【 授权许可】

Unknown