Summary
The synthesis of the bacteriocin cloacin DF13 and its release into the culture medium were genetically uncoupled by subcloning the gene encoding the bacteriocin release protein (BRP) from pCloDF13. The gene was cloned under the control of the IPTG-inducible lpp-lac promoter-operator system on the expression vector pINIIIA1, giving pJL1. A 4 kb DNA fragment of pJL1, containing the tandem lpp-lac promoter, the BRP gene and lacI (BRP cassette), was cloned into the pCloDF13 derivative plasmid pJN67, which encodes cloacin DF13 but not the release protein. Furthermore, the pCloDF13 immunity protein gene was subcloned downstream of the temperature-inducible P L promoter of the expression vector pPLc236, together with the BRP cassette. Growth, induction and excretion experiments with Escherichia coli cells harbouring the constructed plasmids revealed that: i) the BRP is the only pCloDF13-derived gene product responsible for the observed growth inhibition and apparent lysis of strongly induced cells. This growth inhibition and lysis can be prevented by Mg2+ ions added to the culture medium, and involves induction of phospholipase A activity. (ii) The expression of the BRP gene can be regulated by varying the IPTG concentration. (iii) A separately controlled and moderate induced BRP synthesis can be used to bring about the release of large amounts of cloacin DF13 under conditions that allow a strong induction of the bacteriocin and which do not result in lysis of cells. (iiii) Preliminary results indicated that the BRP can stimulate the release of immunity protein in the absence of cloacin or cloacin fragments.
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References
Birnboim HC, Doly J (1979) A rapid alkaline extraction procedure for screening recombinant plasmid DNA. Nucleic Acids Res 7:6727–6738
Casadaban M, Cohen SN (1980) Analysis of gene control signals by DNA fusion and cloning in Escherichia coli. J Mol Biol 138:179–207
Cavard D, Crozel V, Gorvel JP, Pattus F, Baty D, Lazdunski C (1986) A molecular genetic and immunological approach to the functioning of colicin A, a pore-forming protein. J Mol Biol 187:449–459
Chang ACY, Cohen SN (1978) Construction and characterization of amplifiable multicopy DNA cloning vehicles derived from the P15A cryptic miniplasmid. J Bacteriol 134:1141–1156
Cole ST, Saint-Joanis B, Pugsley AP (1985) Molecular characterization of the colicin E2 operon and identification of its products. Mol Gen Genet 198:465–472
Dagert M, Ehrlich SD (1979) Prolonged incubation in calcium chloride improves the competence of Escherichia coli cells. Gene 6:23–28
De Geus P, Van Die I, Bergmans H, Tommassen J, De Haas G (1983) Molecular cloning of pldA the structural gene for outer membrane phospholipase of E. coli K12. Mol Gen Genet 140:150–155
De Graaf FK, Klaasen-Boor P (1977) Purification and characterization of a complex between cloacin and its immunity protein isolated from Enterobacter cloacae (CloDF13). Eur J Biochem 73:107–114
De Graaf FK, Klaasen-Boor (1974) Purification and characterization of the cloacin DF13 immunity protein. FEBS Microbiol Lett 40:293–296
De Graaf FK, Oudega B (1986) Production and release of cloacin DF13 and related colicins. Curr Top Microbiol Immunol 125:183–205
De Graaf FK, Stukart MJ, Boogert FC, Metselaar K (1978) Limited proteolysis of cloacin DF13 and characterization of the cleavage products. Biochemistry 17:1137–1142
Doi D, Ohki M, Nojima S (1972) Two kinds of phospholipase A and lysophospholipase in Escherichia coli. Biochim Biophys Acta 260:244–258
Hakkaart MJJ, Veltkamp E, Nijkamp HJ (1981a) Protein H encoded by plasmid CloDF13 involved in lysis of the bacterial host. I. Localization of the gene and identification and subcellular localization of the gene H product. Mol Gen Genet 183:318–325
Hakkaart MJJ, Veltkamp E, Nijkamp HJJ (1981b) Protein H encoded by plasmid CloDF13 involved in lysis of the bacterial host. II. Functions and regulation of synthesis of the gene H product. Mol Gen Genet 183:326–332
Krone WJA, De Vries P, Koningstein G, De Jong AJR, De Graaf FK, Oudega B (1986) Uptake of cloacin DF13 by susceptible cells: removal of immunity protein and fragmentation of cloacin molecules. J Bacteriol 166:260–268
Luirink J, Van der Sande C, Tommassen J, Veltkamp E, De Graaf FK, Oudega B (1986) Effects of divalent cations and of phospholipase A activity on excretion of cloacin DF13 and lysis of host cells. J Gen Microbiol 132:825–834
Maniatis T, Fritsch EF, Sambrook J (1982) Molecular cloning: a laboratory manual. Cold Spring Harbor Laboratory Press, New York
Masaki H, Ohta T (1985) Colicin E3 and its immunity genes. J Mol Biol 182:217–227
Masui Y, Mizuno T, Inouye M (1984) Novel high level expression cloning vehicles: 104-fold amplification of Escherichia coli minor protein. Biotechnology 2:81–85
Messing J, Crea R, Seeburg PH (1981) A system for shotgun DNA sequencing. Nucleic Acids Res 9:309–321
Ohno-Iwashita Y, Imahori K (1980) Assignment of the functional loci in colicin E2 and E3 molecules by the characterization of their proteolytic fragments. Biochemistry 19:652–659
Oudega B, Klaasen-Boor P, De Graaf FK (1975) Mode of action of the cloacin DF13 immunity protein. Biochim Biophys Acta 392:184–195
Oudega B, Klaasen-Boor P, Sneeuwloper G, De Graaf FK (1977) Interaction of the complex between cloacin and its immunity protein and of cloacin with the outer and cytoplasmic membranes of sensitive cells. Eur J Biochem 78:445–453
Oudega B, Stegehuis F, Van Tiel-Menkveld GJ, De Graaf FK (1982) Protein H encoded by plasmid CloDF13 is involved in excretion of cloacin DF13. J Bacteriol 150:1115–1121
Oudega B, Stegehuis F, De Graaf FK (1984a) Effect of glucose fermentation on the functioning of protein H in the excretion of cloacin DF13 by Escherichia coli. FEMS Microbiol Lett 21:125–131
Oudega B, Ykema A, stegehuis F, De Graaf FK (1984b) Detection and subcellular localization of mature protein H involved in excretion of cloacin DF13. FEMS Microbiol Lett 22:101–108
Pugsley AP, Schwartz M (1983) Expression of a gene in a 400 base pair fragment of plasmid Col E2-P9 is sufficient to cause host cell lysis. J Bacteriol 156:109–114
Pugsley AP, Schwartz M (1984) Colicin E2 release lysis, leakage or secretion? Possible role of phospholipase. EMBO J 3:2393–2397
Remaut E, Stanssers P, Fiers W (1981) Plasmid vectors for high-efficiency expression controlled by the PL promoter of coliphage lambda. Gene 15:81–93
Sanger F, Nicklen S, Coulson AR (1977) DNA sequencing with chain-terminating inhibitors. Proc Natl Acad Sci USA 74:5463–5467
Van den Elzen PJM, Gaastra W, Spelt CE, De Graaf FK, Veltkamp E, Nijkamp HJJ (1980a) Molecular structure of the immunity gene and immunity protein of the bacteriocinogenic plasmid CloDF13. Nucleic Acids Res 8:4349–4363
Van den Elzen PJM, Konings RHN, Veltkamp E, Nijkamp HJJ (1980b) Transpription of bacteriocinogenic plasmid CloDF13 in vivo and in vitro: structure of the cloacin-immunity operon. J Bacteriol 144:579–591
Van den Elzen PJM, Walters HBB, Veltkamp E, Nijkamp HJJ (1983) Molecular structure and function of the bacteriocin gene and bacteriocin protein of plasmid CloDF13. Nucleic Acids Res 11:2465–2477
Van Embden JDA, Veltkamp E, Nijkamp HJJ (1978) Integration of a transposable DNA sequence which mediate ampicillin resistance into CloDF13 plasmid DNA; determination of the sites and orientation of Tn901 insertions. Plasmid 1:204–217
Van Tiel-Menkveld GJ, Rezee A, De Graaf FK (1979) Production and excretion of cloacin DF13 by Escherichia coli harboring plasmid CloDF13. J Bacteriol 140:415–423
Van Tiel-Menkveld GJ, Veltkamp E, De Graaf FK (1981) Mitomycin C-induced synthesis of cloacin DF13 and lethality in cloacinogenic Escherichia coli cells. J Bacteriol 146:41–48
Veltkamp E, Stuitje AR (1981) Replication and structure of the bacteriocinogenic plasmids CloDF13 and ColE1. Plasmid 5:76–99
Warren GJ, Sherratt DJ (1978) Incompatibility and transforming efficiency of Col E1 and related plasmids. Mol Gen Genet 161:39–47
Yamada M, Ebina Y, Miyata T, Nakazawa T, Nakazawa A (1982) Nucleotide sequence of the structural gene for colicin E1 and predicted structure of the protein. Proc Natl Acad Sci USA 79:2827–2831
Yamada M, Nakazawa A (1984) Factors necessary for the export process of colicin E1 across cytoplasmic membrane of Escherichia coli. Eur J Biochem 140:249–255
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Luirink, J., de Graaf, F.K. & Oudega, B. Uncoupling of synthesis and release of cloacin DF13 and its immunity protein by Escherichia coli . Mol Gen Genet 206, 126–132 (1987). https://doi.org/10.1007/BF00326547
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DOI: https://doi.org/10.1007/BF00326547