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PMID:15555931

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Citation

Boshoff, A, Hennessy, F and Blatch, GL (2004) The in vivo and in vitro characterization of DnaK from Agrobacterium tumefaciens RUOR. Protein Expr. Purif. 38:161-9

Abstract

Molecular chaperones of the heat shock protein 70 family (Hsp70; also called DnaK in prokaryotes) play an important role in the folding and functioning of cellular protein machinery. The dnaK gene from the plant pathogen Agrobacterium tumefaciens RUOR was amplified using the polymerase chain reaction and the DnaK protein (Agt DnaK) was over-produced as a His-tagged protein in Escherichia coli. The Agt DnaK amino acid sequence was 96% identical to the A. tumefaciens C58 DnaK sequence and 65% identical to the E. coli DnaK sequence. Agt DnaK was shown to be able to functionally replace E. coli DnaK in vivo using complementation assays with an E. coli dnaK756 mutant strain and a dnaK52 deletion strain. Over-production and purification of Agt DnaK was successful, and allowed for further characterization of the protein. Kinetic analysis of the basal ATPase activity of purified Agt DnaK revealed a Vmax of 1.3 nmol phosphate released per minute per milligram DnaK, and a Km of 62 microM ATP. Thus, this is the first study to provide both in vivo and in vitro evidence that Agt DnaK has the properties of a molecular chaperone of the Hsp70 family.

Links

PubMed Online version:10.1016/j.pep.2004.06.039

Keywords

Adenosine Triphosphatases/metabolism; Adenosine Triphosphate/metabolism; Agrobacterium tumefaciens/genetics; Amino Acid Sequence; Bacterial Proteins/biosynthesis; Bacterial Proteins/genetics; Bacterial Proteins/isolation & purification; Escherichia coli Proteins/genetics; Gene Expression Regulation, Bacterial; Genetic Complementation Test; HSP70 Heat-Shock Proteins/biosynthesis; HSP70 Heat-Shock Proteins/genetics; HSP70 Heat-Shock Proteins/isolation & purification; Hydrolysis; Molecular Sequence Data; Sequence Homology, Amino Acid

Significance

Annotations

Gene product Qualifier GO Term Evidence Code with/from Aspect Extension Notes Status

RHIRD:Q6RSN6

GO:0016887: ATPase activity

ECO:0000314:

F

Direct ATPase activity after functional complementation of mutant with cloned gene as shown in Figure 5 on page 167.

complete
CACAO 5018


See also

References

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