Analysis of lambda receptor and beta-lactamase synthesis and export using cloned genes in a minicell system |
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Authors: | Jean-Marie Clement David Perrin and Joe Hedgpeth |
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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 |
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Abstract: | Summary We have cloned lamB, the gene for receptor (an outer membrane protein), on a small plasmid which also carries the gene for -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 receptor and -lactamase are made as full length precursors which are subsequently processed. We also show that the receptor precursor can be exported to the outer membrane before it is processed. Mature -lactamase is found only in the periplasm, suggesting that processing may be a requirement for export to the periplasm. |
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