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1.
Biosci Biotechnol Biochem ; 66(7): 1515-23, 2002 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-12224635

RESUMO

Escherichia coli SpoT protein, with 702 amino acid residues, is a bifunctional enzyme catalyzing both guanosine 5'-diphosphate 3'-diphosphate (ppGpp) degradation and its synthesis. First, we investigated how many domains are included in SpoT protein, by limited hydrolysis of the protein with serine proteases, alpha-chymotrypsin, and elastase. Based on the results, we deduced that SpoT protein is composed of two major domains, an N-terminal half domain from Met1 to Phe373 and a C-terminal half domain from Glu374 to Asn702 (C-terminal end). In addition, by a further alpha-chymotrypsin digestion, two cleaved sites were found at Arg196 in the N-terminal half domain (D12) and at Lys475 in the C-terminal half domain (D34), to produce four minor domains, D1, D2, D3, and D4. Next, plasmids expressing the two major domains (D12 and D34) and four minor domains (D1, D2, D3, and D4) were constructed. Consequently, the deduced SpoT minor domains as well as the major domains were expressed as stable protein units, except for D4. D4 may also be folded into a stable protein in E. coli cells, since high expression of D4 from a plasmid results in host cell lethality. E. coli relA -, spoT- double null strains expressing D1, D2, and D12 recovered cell growth in M9 minimal medium, but the transformants of D3, D4, and D34 did not grow in the minimal medium. This indicates that ppGpp synthetic activities could be restricted in the N-terminal half domain (D12, D1, and D2).


Assuntos
Escherichia coli/genética , Escherichia coli/metabolismo , Guanosina Tetrafosfato/biossíntese , Pirofosfatases/genética , Pirofosfatases/metabolismo , Western Blotting , Meios de Cultura , Primers do DNA , Eletroforese em Gel de Poliacrilamida , Escherichia coli/crescimento & desenvolvimento , Regulação Bacteriana da Expressão Gênica/genética , Plasmídeos/genética , Estrutura Terciária de Proteína/genética , Serina Endopeptidases/química
2.
Biosci Biotechnol Biochem ; 66(12): 2735-8, 2002 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-12596879

RESUMO

Amino acid substitutions were introduced into a structurally flexible and highly conserved region of Escherichia coli SpoT protein. SpoT protein changed from Asp to Ala at the 293rd position did not restore cell growth of E. coli CF8295 (delta relA, delta spoT) and did not accumulate ppGpp in the cell, suggesting that the Asp293 is indispensable for ppGpp synthesis of the protein.


Assuntos
Escherichia coli/enzimologia , Guanosina Tetrafosfato/metabolismo , Pirofosfatases/química , Pirofosfatases/metabolismo , Alanina/genética , Sequência de Aminoácidos , Substituição de Aminoácidos , Ácido Aspártico/genética , Divisão Celular , Escherichia coli/crescimento & desenvolvimento , Escherichia coli/metabolismo , Guanosina Tetrafosfato/biossíntese , Dados de Sequência Molecular , Mutação , Pirofosfatases/genética
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