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Analysis of lambda receptor and beta-lactamase synthesis and export using cloned genes in a minicell system
Authors:Jean-Marie Clement  David Perrin and Joe Hedgpeth
Institution:(1) Institut Pasteuer, 28 rue du Dr. Roux, Paris, France;(2) Howard Hughes Medical Inst., Department of Biochemistry, Univ. of California, 94143 San Francisco, CA, USA;(3) Present address: Howard Hughes Medical Institute, Department of Biochemistry and Biophysics, University of California, San Francisco;(4) HSE 1504, University of California, San Francisco, 94143 San Francisco, CA, USA
Abstract:Summary We have cloned lamB, the gene for lambda receptor (an outer membrane protein), on a small plasmid which also carries the gene for beta-lactamase (a periplasmic protein). We have identified a promoter in the region of malK, the gene immediately preceding lamB, which is active in minicells but relatively inactive in vitro. Using a minicell system, we have found that both lambda receptor and beta-lactamase are made as full length precursors which are subsequently processed. We also show that the lambda receptor precursor can be exported to the outer membrane before it is processed. Mature beta-lactamase is found only in the periplasm, suggesting that processing may be a requirement for export to the periplasm.
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