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The transcription start sites for the tatABCD and tatE loci, encoding components of the Tat (twin-arginine translocase) protein export pathway, have been identified. Expression studies indicate that the tatABCD and tatE transcription units are expressed constitutively. Translational fusion experiments suggest that TatA is synthesized at a much higher level than the other Tat proteins.

Original publication

DOI

10.1128/JB.183.5.1801-1804.2001

Type

Journal article

Journal

J Bacteriol

Publication Date

03/2001

Volume

183

Pages

1801 - 1804

Keywords

Aerobiosis, Anaerobiosis, Base Sequence, Carrier Proteins, Escherichia coli, Escherichia coli Proteins, Gene Expression Regulation, Bacterial, Membrane Transport Proteins, Molecular Sequence Data, Transcription, Genetic