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. 1994 Jun 1;300(Pt 2):599–603. doi: 10.1042/bj3000599

Cloning and expression in Bacillus subtilis of the npr gene from Bacillus thermoproteolyticus Rokko coding for the thermostable metalloprotease thermolysin.

M J O'Donohue 1, B P Roques 1, A Beaumont 1
PMCID: PMC1138203  PMID: 8002967

Abstract

We report the isolation, cloning and expression, in Bacillus subtilis, of the gene coding for thermolysin, a thermostable metalloprotease which is produced by Bacillus thermoproteolyticus Rokko. The nucleotide sequence has revealed that, like neutral proteases produced by other members of the Bacillus species, thermolysin is probably produced as a preproenzyme carrying a typical N-terminal membrane signal sequence. Further, the thermolysin gene shares a strong homology with two other previously cloned genes from two different strains of Bacillus stearothermophilus. The sequence of the mature secreted protease, inferred from the DNA sequence, is, with two exceptions, identical with the previously published protein sequence of thermolysin [Titani, Hermodson, Ericsson, Walsh and Neurath (1972) Nature (London) 238, 35-37]. The exceptions are Asn37 and Gln119, originally reported to be Asp and Glu respectively. The biochemical characterization of the secreted recombinant protein shows that it is indistinguishable from the wild-type thermolysin.

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  1. Aoki T., Noguchi N., Sasatsu M., Kono M. Complete nucleotide sequence of pTZ12, a chloramphenicol-resistance plasmid of Bacillus subtilis. Gene. 1987;51(1):107–111. doi: 10.1016/0378-1119(87)90481-1. [DOI] [PubMed] [Google Scholar]
  2. Bode W., Gomis-Rüth F. X., Huber R., Zwilling R., Stöcker W. Structure of astacin and implications for activation of astacins and zinc-ligation of collagenases. Nature. 1992 Jul 9;358(6382):164–167. doi: 10.1038/358164a0. [DOI] [PubMed] [Google Scholar]
  3. Bradford M. M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem. 1976 May 7;72:248–254. doi: 10.1006/abio.1976.9999. [DOI] [PubMed] [Google Scholar]
  4. Chang S., Cohen S. N. High frequency transformation of Bacillus subtilis protoplasts by plasmid DNA. Mol Gen Genet. 1979 Jan 5;168(1):111–115. doi: 10.1007/BF00267940. [DOI] [PubMed] [Google Scholar]
  5. Cheng Y., Prusoff W. H. Relationship between the inhibition constant (K1) and the concentration of inhibitor which causes 50 per cent inhibition (I50) of an enzymatic reaction. Biochem Pharmacol. 1973 Dec 1;22(23):3099–3108. doi: 10.1016/0006-2952(73)90196-2. [DOI] [PubMed] [Google Scholar]
  6. Eijsink V. G., Vriend G., Van Den Burg B., Venema G., Stulp B. K. Contribution of the C-terminal amino acid to the stability of Bacillus subtilis neutral protease. Protein Eng. 1990 Oct;4(1):99–104. doi: 10.1093/protein/4.1.99. [DOI] [PubMed] [Google Scholar]
  7. Gomis-Rüth F. X., Stöcker W., Huber R., Zwilling R., Bode W. Refined 1.8 A X-ray crystal structure of astacin, a zinc-endopeptidase from the crayfish Astacus astacus L. Structure determination, refinement, molecular structure and comparison with thermolysin. J Mol Biol. 1993 Feb 20;229(4):945–968. doi: 10.1006/jmbi.1993.1098. [DOI] [PubMed] [Google Scholar]
  8. Kubo M., Imanaka T. Cloning and nucleotide sequence of the highly thermostable neutral protease gene from Bacillus stearothermophilus. J Gen Microbiol. 1988 Jul;134(7):1883–1892. doi: 10.1099/00221287-134-7-1883. [DOI] [PubMed] [Google Scholar]
  9. Nicoletti V. G., Condorelli D. F. Optimized PEG method for rapid plasmid DNA purification: high yield from "midi-prep". Biotechniques. 1993 Apr;14(4):532-4, 536. [PubMed] [Google Scholar]
  10. Nishiya Y., Imanaka T. Cloning and nucleotide sequences of the Bacillus stearothermophilus neutral protease gene and its transcriptional activator gene. J Bacteriol. 1990 Sep;172(9):4861–4869. doi: 10.1128/jb.172.9.4861-4869.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Pauptit R. A., Karlsson R., Picot D., Jenkins J. A., Niklaus-Reimer A. S., Jansonius J. N. Crystal structure of neutral protease from Bacillus cereus refined at 3.0 A resolution and comparison with the homologous but more thermostable enzyme thermolysin. J Mol Biol. 1988 Feb 5;199(3):525–537. doi: 10.1016/0022-2836(88)90623-7. [DOI] [PubMed] [Google Scholar]
  12. Roques B. P., Beaumont A. Neutral endopeptidase-24.11 inhibitors: from analgesics to antihypertensives? Trends Pharmacol Sci. 1990 Jun;11(6):245–249. doi: 10.1016/0165-6147(90)90252-4. [DOI] [PubMed] [Google Scholar]
  13. Roques B. P., Fournié-Zaluski M. C., Soroca E., Lecomte J. M., Malfroy B., Llorens C., Schwartz J. C. The enkephalinase inhibitor thiorphan shows antinociceptive activity in mice. Nature. 1980 Nov 20;288(5788):286–288. doi: 10.1038/288286a0. [DOI] [PubMed] [Google Scholar]
  14. Roques B. P., Noble F., Daugé V., Fournié-Zaluski M. C., Beaumont A. Neutral endopeptidase 24.11: structure, inhibition, and experimental and clinical pharmacology. Pharmacol Rev. 1993 Mar;45(1):87–146. [PubMed] [Google Scholar]
  15. Sanger F., Nicklen S., Coulson A. R. DNA sequencing with chain-terminating inhibitors. Proc Natl Acad Sci U S A. 1977 Dec;74(12):5463–5467. doi: 10.1073/pnas.74.12.5463. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Simonen M., Palva I. Protein secretion in Bacillus species. Microbiol Rev. 1993 Mar;57(1):109–137. doi: 10.1128/mr.57.1.109-137.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Takagi M., Imanaka T., Aiba S. Nucleotide sequence and promoter region for the neutral protease gene from Bacillus stearothermophilus. J Bacteriol. 1985 Sep;163(3):824–831. doi: 10.1128/jb.163.3.824-831.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Vogel Z., Altstein M. The adsorption of enkephalin to porous polystyrene beads: a simple assay for enkephalin hydrolysis. FEBS Lett. 1977 Aug 15;80(2):332–336. doi: 10.1016/0014-5793(77)80469-9. [DOI] [PubMed] [Google Scholar]
  19. Waksman G., Bouboutou R., Devin J., Besselievre R., Fournie-Zaluski M. C., Roques B. P. Binding of the bidentate inhibitor [3H]HACBO-Gly to the rat brain neutral endopeptidase "enkephalinase". Biochem Biophys Res Commun. 1985 Aug 30;131(1):262–268. doi: 10.1016/0006-291x(85)91797-8. [DOI] [PubMed] [Google Scholar]
  20. Yanisch-Perron C., Vieira J., Messing J. Improved M13 phage cloning vectors and host strains: nucleotide sequences of the M13mp18 and pUC19 vectors. Gene. 1985;33(1):103–119. doi: 10.1016/0378-1119(85)90120-9. [DOI] [PubMed] [Google Scholar]
  21. van den Burg B., Enequist H. G., van der Haar M. E., Eijsink V. G., Stulp B. K., Venema G. A highly thermostable neutral protease from Bacillus caldolyticus: cloning and expression of the gene in Bacillus subtilis and characterization of the gene product. J Bacteriol. 1991 Jul;173(13):4107–4115. doi: 10.1128/jb.173.13.4107-4115.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]

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