Abstract |
A gene termed cbhE' was cloned from the QpH1 plasmid of Coxiella burnetii. Expression of recombinants containing cbhE' in vitro and in Escherichia coli maxicells, produced an insert-encoded polypeptide of approx. 42 kDa. The CbhE protein was not cleaved when intact maxicells were treated with trypsin. Hybridizations of total DNA isolated from the six strains of C. burnetii indicate that this gene is unique to C. burnetii strains associated with acute disease, i.e., Hamilton[I], Vacca[II], and Rasche[III]. The cbhE' gene was not detected in strains associated with chronic disease (Biotzere[IV] and Corazon[V]) or the Dod[VI] strain. The cbhE' open reading frame (ORF) is 1022 bp in length and is preceded by a predicted promoter/Shine-Dalgarno (SD) region of TCAACT(-35)-N16-TAAAAT(-10)-N14-AGAAGGA (SD) located 10 nucleotides (nt) before the presumed AUG start codon. The ORF ends with a single UAA stop codon and has no apparent Rho-factor-independent terminator following it. The cbhE' gene codes for the CbhE protein of 341 amino acid (aa) residues with a deduced Mr of 39,442. CbhE is predominantly hydrophilic with a predicted pI of 4.43. The function of CbhE is unknown. No nt or aa sequences with homology to cbhE' or CbhE, respectively, were found in searches of a number of data bases.
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Authors | M F Minnick, C L Small, M E Frazier, L P Mallavia |
Journal | Gene
(Gene)
Vol. 103
Issue 1
Pg. 113-8
(Jul 15 1991)
ISSN: 0378-1119 [Print] Netherlands |
PMID | 1879692
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)
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Chemical References |
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Topics |
- Acute Disease
- Amino Acid Sequence
- Bacterial Proteins
(biosynthesis, chemistry, genetics)
- Base Sequence
- Cloning, Molecular
- Coxiella
(genetics, pathogenicity)
- Gene Expression
(physiology)
- Molecular Sequence Data
- Nucleic Acid Hybridization
- Open Reading Frames
(genetics)
- Plasmids
(genetics)
- Promoter Regions, Genetic
(genetics)
- Q Fever
(microbiology)
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