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. 1995 Nov;177(21):6033–6040. doi: 10.1128/jb.177.21.6033-6040.1995

Isolation and characterization of two genes encoding proteases associated with the mycelium of Streptomyces lividans 66.

C Binnie 1, M J Butler 1, J S Aphale 1, R Bourgault 1, M A DiZonno 1, P Krygsman 1, L Liao 1, E Walczyk 1, L T Malek 1
PMCID: PMC177439  PMID: 7592364

Abstract

A strain of Streptomyces lividans 66 deleted for a major tripeptidyl aminopeptidase (Tap) was used as a host to screen an S. lividans genomic library for clones overexpressing activity against the chromogenic substrate Ala-Pro-Ala-beta-naphthylamide. In addition to reisolation of the tap gene, clones representing another locus, slpD, were uncovered. slpD was analyzed by deletion subcloning to localize its functional sequence. Nucleotide sequence determination revealed an open reading frame encoding a 55-kDa protein exhibiting significant amino acid sequence homology to Tap, particularly around the putative active-site serine residue. No secreted protein was observed for strains harboring the slpD clone, but inspection of the predicted protein sequence revealed a putative lipoprotein signal peptide (signal peptidase II type), suggesting a mycelial location for the SlpD proteinase. In an attempt to isolate an endoprotease known to be active against some heterologous proteins, a second clone was isolated by using a longer substrate (t-butyloxycarbonyl [Boc]-APARSPA-beta-naphthylamide) containing a chemical blocking group at the amino terminus to prevent aminopeptidase cleavage. This locus, slpE, appeared to also encode a 55-kDa mycelium-associated (lipoprotein) proteinase, whose predicted protein sequences showed significant amino acid homology to Tap and SlpD, particularly around the putative active-site serine residues. Chromosomal integration and deletion analysis in both the wild-type and Tap-deficient backgrounds appeared to indicate that SlpD was essential for viability and SlpE was required for growth on minimal media.

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Selected References

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  1. Anné J., Van Mellaert L. Streptomyces lividans as host for heterologous protein production. FEMS Microbiol Lett. 1993 Dec 1;114(2):121–128. doi: 10.1111/j.1574-6968.1993.tb06561.x. [DOI] [PubMed] [Google Scholar]
  2. Blow D. Enzymology. More of the catalytic triad. Nature. 1990 Feb 22;343(6260):694–695. doi: 10.1038/343694a0. [DOI] [PubMed] [Google Scholar]
  3. Brawner M., Poste G., Rosenberg M., Westpheling J. Streptomyces: a host for heterologous gene expression. Curr Opin Biotechnol. 1991 Oct;2(5):674–681. doi: 10.1016/0958-1669(91)90033-2. [DOI] [PubMed] [Google Scholar]
  4. Butler M. J., Bergeron A., Soostmeyer G., Zimny T., Malek L. T. Cloning and characterisation of an aminopeptidase P-encoding gene from Streptomyces lividans. Gene. 1993 Jan 15;123(1):115–119. doi: 10.1016/0378-1119(93)90549-i. [DOI] [PubMed] [Google Scholar]
  5. Butler M. J., Binnie C., DiZonno M. A., Krygsman P., Soltes G. A., Soostmeyer G., Walczyk E., Malek L. T. Cloning and characterization of a gene encoding a secreted tripeptidyl aminopeptidase from Streptomyces lividans 66. Appl Environ Microbiol. 1995 Aug;61(8):3145–3150. doi: 10.1128/aem.61.8.3145-3150.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Butler M. J., Davey C. C., Krygsman P., Walczyk E., Malek L. T. Cloning of genetic loci involved in endoprotease activity in Streptomyces lividans 66: a novel neutral protease gene with an adjacent divergent putative regulatory gene. Can J Microbiol. 1992 Sep;38(9):912–920. doi: 10.1139/m92-148. [DOI] [PubMed] [Google Scholar]
  7. Doggett P. E., Blattner F. R. Personal access to sequence databases on personal computers. Nucleic Acids Res. 1986 Jan 10;14(1):611–619. doi: 10.1093/nar/14.1.611. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Haandrikman A. J., Meesters R., Laan H., Konings W. N., Kok J., Venema G. Processing of the lactococcal extracellular serine proteinase. Appl Environ Microbiol. 1991 Jul;57(7):1899–1904. doi: 10.1128/aem.57.7.1899-1904.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Henderson G., Krygsman P., Liu C. J., Davey C. C., Malek L. T. Characterization and structure of genes for proteases A and B from Streptomyces griseus. J Bacteriol. 1987 Aug;169(8):3778–3784. doi: 10.1128/jb.169.8.3778-3784.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Ingram C., Brawner M., Youngman P., Westpheling J. xylE functions as an efficient reporter gene in Streptomyces spp.: use for the study of galP1, a catabolite-controlled promoter. J Bacteriol. 1989 Dec;171(12):6617–6624. doi: 10.1128/jb.171.12.6617-6624.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Krieger T. J., Bartfeld D., Jenish D. L., Hadary D. Purification and characterization of a novel tripeptidyl aminopeptidase from Streptomyces lividans 66. FEBS Lett. 1994 Oct 3;352(3):385–388. doi: 10.1016/0014-5793(94)00988-0. [DOI] [PubMed] [Google Scholar]
  12. Strickler J. E., Berka T. R., Gorniak J., Fornwald J., Keys R., Rowland J. J., Rosenberg M., Taylor D. P. Two novel Streptomyces protein protease inhibitors. Purification, activity, cloning, and expression. J Biol Chem. 1992 Feb 15;267(5):3236–3241. [PubMed] [Google Scholar]
  13. Vos P., Simons G., Siezen R. J., de Vos W. M. Primary structure and organization of the gene for a procaryotic, cell envelope-located serine proteinase. J Biol Chem. 1989 Aug 15;264(23):13579–13585. [PubMed] [Google Scholar]
  14. von Heijne G. The structure of signal peptides from bacterial lipoproteins. Protein Eng. 1989 May;2(7):531–534. doi: 10.1093/protein/2.7.531. [DOI] [PubMed] [Google Scholar]

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