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. 1996 Mar;178(6):1539–1547. doi: 10.1128/jb.178.6.1539-1547.1996

Cloning, sequencing, and expression of the gene encoding a large S-layer-associated endoxylanase from Thermoanaerobacterium sp. strain JW/SL-YS 485 in Escherichia coli.

S Y Liu 1, F C Gherardini 1, M Matuschek 1, H Bahl 1, J Wiegel 1
PMCID: PMC177836  PMID: 8626279

Abstract

The gene (xynA) encoding a surface-exposed, S-layer-associated endoxylanase from Thermoanaerobacterium sp. strain JW/SL-YS 485 was cloned and expressed in Escherichia coli. A 3.8-kb fragment was amplified from chromosomal DNA by using primers directed against conserved sequences of endoxylanases isolated from other thermophilic bacteria. This PCR product was used as a probe in Southern hybridizations to identify a 4.6-kb EcoRI fragment containing the complete xynA gene. This fragment was cloned into E. coli, and recombinant clones expressed significant levels of xylanase activity. The purified recombinant protein had an estimated molecular mass (150 kDa), temperature maximum (80 degrees C), pH optimum (pH 6.3), and isoelectric point (pH 4.5) that were similar to those of the endoxylanase isolated from strain JW/SL-YS 485. The entire insert was sequenced and analysis revealed a 4,044-bp open reading frame encoding a protein containing 1,348 amino acid residues (estimated molecular mass of 148 kDa).xynA was preceded by a putative promoter at -35 (TTAAT) and -10 (TATATT) and a potential ribosome binding site (AGGGAG) and was expressed constitutively in E. coli. The deduced amino acid sequence showed 30 to 96% similarity to sequences of family F beta-glycanases. A putative 32-amino-acid signal peptide was identified, and the C-terminal end of the protein contained three repeating sequences 59, 64, and 57 amino acids) that showed 46 to 68% similarity to repeating sequences at the N-terminal end of S-layer and S-layer-associated proteins from other gram-positive bacteria. These repeats could permit an interaction of the enzyme with the S-layer and tether it to the cell surface.

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Selected References

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  1. Ames G. F., Prody C., Kustu S. Simple, rapid, and quantitative release of periplasmic proteins by chloroform. J Bacteriol. 1984 Dec;160(3):1181–1183. doi: 10.1128/jb.160.3.1181-1183.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Biely P., Markovic O., Mislovicová D. Sensitive detection of endo-1,4-beta-glucanases and endo-1,4-beta-xylanases in gels. Anal Biochem. 1985 Jan;144(1):147–151. doi: 10.1016/0003-2697(85)90096-x. [DOI] [PubMed] [Google Scholar]
  3. Birnboim H. C., Doly J. A rapid alkaline extraction procedure for screening recombinant plasmid DNA. Nucleic Acids Res. 1979 Nov 24;7(6):1513–1523. doi: 10.1093/nar/7.6.1513. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Bowditch R. D., Baumann P., Yousten A. A. Cloning and sequencing of the gene encoding a 125-kilodalton surface-layer protein from Bacillus sphaericus 2362 and of a related cryptic gene. J Bacteriol. 1989 Aug;171(8):4178–4188. doi: 10.1128/jb.171.8.4178-4188.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. 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]
  6. Brockman R. W., Heppel L. A. On the localization of alkaline phosphatase and cyclic phosphodiesterase in Escherichia coli. Biochemistry. 1968 Jul;7(7):2554–2562. doi: 10.1021/bi00847a016. [DOI] [PubMed] [Google Scholar]
  7. Clarke J. H., Laurie J. I., Gilbert H. J., Hazlewood G. P. Multiple xylanases of Cellulomonas fimi are encoded by distinct genes. FEMS Microbiol Lett. 1991 Oct 15;67(3):305–309. doi: 10.1016/0378-1097(91)90493-t. [DOI] [PubMed] [Google Scholar]
  8. Coughlan M. P., Hazlewood G. P. beta-1,4-D-xylan-degrading enzyme systems: biochemistry, molecular biology and applications. Biotechnol Appl Biochem. 1993 Jun;17(Pt 3):259–289. [PubMed] [Google Scholar]
  9. Devereux J., Haeberli P., Smithies O. A comprehensive set of sequence analysis programs for the VAX. Nucleic Acids Res. 1984 Jan 11;12(1 Pt 1):387–395. doi: 10.1093/nar/12.1part1.387. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Egelseer E., Schocher I., Sára M., Sleytr U. B. The S-layer from Bacillus stearothermophilus DSM 2358 functions as an adhesion site for a high-molecular-weight amylase. J Bacteriol. 1995 Mar;177(6):1444–1451. doi: 10.1128/jb.177.6.1444-1451.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Engel A. M., Cejka Z., Lupas A., Lottspeich F., Baumeister W. Isolation and cloning of Omp alpha, a coiled-coil protein spanning the periplasmic space of the ancestral eubacterium Thermotoga maritima. EMBO J. 1992 Dec;11(12):4369–4378. doi: 10.1002/j.1460-2075.1992.tb05537.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Etienne-Toumelin I., Sirard J. C., Duflot E., Mock M., Fouet A. Characterization of the Bacillus anthracis S-layer: cloning and sequencing of the structural gene. J Bacteriol. 1995 Feb;177(3):614–620. doi: 10.1128/jb.177.3.614-620.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Faraldo M. M., de Pedro M. A., Berenguer J. Sequence of the S-layer gene of Thermus thermophilus HB8 and functionality of its promoter in Escherichia coli. J Bacteriol. 1992 Nov;174(22):7458–7462. doi: 10.1128/jb.174.22.7458-7462.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Freier Doris, Mothershed Cheryle P., Wiegel Juergen. Characterization of Clostridium thermocellum JW20. Appl Environ Microbiol. 1988 Jan;54(1):204–211. doi: 10.1128/aem.54.1.204-211.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Fujino T., Béguin P., Aubert J. P. Organization of a Clostridium thermocellum gene cluster encoding the cellulosomal scaffolding protein CipA and a protein possibly involved in attachment of the cellulosome to the cell surface. J Bacteriol. 1993 Apr;175(7):1891–1899. doi: 10.1128/jb.175.7.1891-1899.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Gilkes N. R., Henrissat B., Kilburn D. G., Miller R. C., Jr, Warren R. A. Domains in microbial beta-1, 4-glycanases: sequence conservation, function, and enzyme families. Microbiol Rev. 1991 Jun;55(2):303–315. doi: 10.1128/mr.55.2.303-315.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Gosalbes M. J., Pérez-González J. A., González R., Navarro A. Two beta-glycanase genes are clustered in Bacillus polymyxa: molecular cloning, expression, and sequence analysis of genes encoding a xylanase and an endo-beta-(1,3)-(1,4)-glucanase. J Bacteriol. 1991 Dec;173(23):7705–7710. doi: 10.1128/jb.173.23.7705-7710.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Grépinet O., Chebrou M. C., Béguin P. Nucleotide sequence and deletion analysis of the xylanase gene (xynZ) of Clostridium thermocellum. J Bacteriol. 1988 Oct;170(10):4582–4588. doi: 10.1128/jb.170.10.4582-4588.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Hall J., Hazlewood G. P., Huskisson N. S., Durrant A. J., Gilbert H. J. Conserved serine-rich sequences in xylanase and cellulase from Pseudomonas fluorescens subspecies cellulosa: internal signal sequence and unusual protein processing. Mol Microbiol. 1989 Sep;3(9):1211–1219. doi: 10.1111/j.1365-2958.1989.tb00271.x. [DOI] [PubMed] [Google Scholar]
  20. Ito K., Ikemasu T., Ishikawa T. Cloning and sequencing of the xynA gene encoding xylanase A of Aspergillus kawachii. Biosci Biotechnol Biochem. 1992 Jun;56(6):906–912. doi: 10.1271/bbb.56.906. [DOI] [PubMed] [Google Scholar]
  21. Kellett L. E., Poole D. M., Ferreira L. M., Durrant A. J., Hazlewood G. P., Gilbert H. J. Xylanase B and an arabinofuranosidase from Pseudomonas fluorescens subsp. cellulosa contain identical cellulose-binding domains and are encoded by adjacent genes. Biochem J. 1990 Dec 1;272(2):369–376. doi: 10.1042/bj2720369. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Kuen B., Sleytr U. B., Lubitz W. Sequence analysis of the sbsA gene encoding the 130-kDa surface-layer protein of Bacillus stearothermophilus strain PV72. Gene. 1994 Jul 22;145(1):115–120. doi: 10.1016/0378-1119(94)90332-8. [DOI] [PubMed] [Google Scholar]
  23. Laemmli U. K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970 Aug 15;227(5259):680–685. doi: 10.1038/227680a0. [DOI] [PubMed] [Google Scholar]
  24. Lee Y. E., Lowe S. E., Henrissat B., Zeikus J. G. Characterization of the active site and thermostability regions of endoxylanase from Thermoanaerobacterium saccharolyticum B6A-RI. J Bacteriol. 1993 Sep;175(18):5890–5898. doi: 10.1128/jb.175.18.5890-5898.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Lee Y. E., Lowe S. E., Zeikus J. G. Gene cloning, sequencing, and biochemical characterization of endoxylanase from Thermoanaerobacterium saccharolyticum B6A-RI. Appl Environ Microbiol. 1993 Sep;59(9):3134–3137. doi: 10.1128/aem.59.9.3134-3137.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Lever M. Colorimetric and fluorometric carbohydrate determination with p-hydroxybenzoic acid hydrazide. Biochem Med. 1973 Apr;7(2):274–281. doi: 10.1016/0006-2944(73)90083-5. [DOI] [PubMed] [Google Scholar]
  27. Lin L. L., Thomson J. A. Cloning, sequencing and expression of a gene encoding a 73 kDa xylanase enzyme from the rumen anaerobe Butyrivibrio fibrisolvens H17c. Mol Gen Genet. 1991 Aug;228(1-2):55–61. doi: 10.1007/BF00282447. [DOI] [PubMed] [Google Scholar]
  28. Lupas A., Engelhardt H., Peters J., Santarius U., Volker S., Baumeister W. Domain structure of the Acetogenium kivui surface layer revealed by electron crystallography and sequence analysis. J Bacteriol. 1994 Mar;176(5):1224–1233. doi: 10.1128/jb.176.5.1224-1233.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Lüthi E., Jasmat N. B., Bergquist P. L. Xylanase from the extremely thermophilic bacterium "Caldocellum saccharolyticum": overexpression of the gene in Escherichia coli and characterization of the gene product. Appl Environ Microbiol. 1990 Sep;56(9):2677–2683. doi: 10.1128/aem.56.9.2677-2683.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Lüthi E., Love D. R., McAnulty J., Wallace C., Caughey P. A., Saul D., Bergquist P. L. Cloning, sequence analysis, and expression of genes encoding xylan-degrading enzymes from the thermophile "Caldocellum saccharolyticum". Appl Environ Microbiol. 1990 Apr;56(4):1017–1024. doi: 10.1128/aem.56.4.1017-1024.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Mannarelli B. M., Evans S., Lee D. Cloning, sequencing, and expression of a xylanase gene from the anaerobic ruminal bacterium Butyrivibrio fibrisolvens. J Bacteriol. 1990 Aug;172(8):4247–4254. doi: 10.1128/jb.172.8.4247-4254.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Matuschek M., Burchhardt G., Sahm K., Bahl H. Pullulanase of Thermoanaerobacterium thermosulfurigenes EM1 (Clostridium thermosulfurogenes): molecular analysis of the gene, composite structure of the enzyme, and a common model for its attachment to the cell surface. J Bacteriol. 1994 Jun;176(11):3295–3302. doi: 10.1128/jb.176.11.3295-3302.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Messner P., Sleytr U. B. Crystalline bacterial cell-surface layers. Adv Microb Physiol. 1992;33:213–275. doi: 10.1016/s0065-2911(08)60218-0. [DOI] [PubMed] [Google Scholar]
  34. Morosoli R., Durand S., Moreau A. Cloning and expression in Escherichia coli of a xylanase-encoding gene from the yeast Cryptococcus albidus. Gene. 1992 Aug 1;117(1):145–150. doi: 10.1016/0378-1119(92)90504-i. [DOI] [PubMed] [Google Scholar]
  35. Ozaki K., Shikata S., Kawai S., Ito S., Okamoto K. Molecular cloning and nucleotide sequence of a gene for alkaline cellulase from Bacillus sp. KSM-635. J Gen Microbiol. 1990 Jul;136(7):1327–1334. doi: 10.1099/00221287-136-7-1327. [DOI] [PubMed] [Google Scholar]
  36. Panbangred W., Kondo T., Negoro S., Shinmyo A., Okada H. Molecular cloning of the genes for xylan degradation of Bacillus pumilus and their expression in Escherichia coli. Mol Gen Genet. 1983;192(3):335–341. doi: 10.1007/BF00392172. [DOI] [PubMed] [Google Scholar]
  37. Peters J., Peters M., Lottspeich F., Baumeister W. S-layer protein gene of Acetogenium kivui: cloning and expression in Escherichia coli and determination of the nucleotide sequence. J Bacteriol. 1989 Nov;171(11):6307–6315. doi: 10.1128/jb.171.11.6307-6315.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  38. 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]
  39. Saul D. J., Williams L. C., Love D. R., Chamley L. W., Bergquist P. L. Nucleotide sequence of a gene from Caldocellum saccharolyticum encoding for exocellulase and endocellulase activity. Nucleic Acids Res. 1989 Jan 11;17(1):439–439. doi: 10.1093/nar/17.1.439. [DOI] [PMC free article] [PubMed] [Google Scholar]
  40. Shao W., Deblois S., Wiegel J. A High-Molecular-Weight, Cell-Associated Xylanase Isolated from Exponentially Growing Thermoanaerobacterium sp. Strain JW/SL-YS485. Appl Environ Microbiol. 1995 Mar;61(3):937–940. doi: 10.1128/aem.61.3.937-940.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  41. Shao W., Obi S., Puls J., Wiegel J. Purification and Characterization of the (alpha)-Glucuronidase from Thermoanaerobacterium sp. Strain JW/SL-YS485, an Important Enzyme for the Utilization of Substituted Xylans. Appl Environ Microbiol. 1995 Mar;61(3):1077–1081. doi: 10.1128/aem.61.3.1077-1081.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  42. Shao W., Wiegel J. Purification and characterization of two thermostable acetyl xylan esterases from Thermoanaerobacterium sp. strain JW/SL-YS485. Appl Environ Microbiol. 1995 Feb;61(2):729–733. doi: 10.1128/aem.61.2.729-733.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  43. Shareck F., Roy C., Yaguchi M., Morosoli R., Kluepfel D. Sequences of three genes specifying xylanases in Streptomyces lividans. Gene. 1991 Oct 30;107(1):75–82. doi: 10.1016/0378-1119(91)90299-q. [DOI] [PubMed] [Google Scholar]
  44. Simpson H. D., Haufler U. R., Daniel R. M. An extremely thermostable xylanase from the thermophilic eubacterium Thermotoga. Biochem J. 1991 Jul 15;277(Pt 2):413–417. doi: 10.1042/bj2770413. [DOI] [PMC free article] [PubMed] [Google Scholar]
  45. Sipat A., Taylor K. A., Lo R. Y., Forsberg C. W., Krell P. J. Molecular cloning of a xylanase gene from Bacteroides succinogenes and its expression in Escherichia coli. Appl Environ Microbiol. 1987 Mar;53(3):477–481. doi: 10.1128/aem.53.3.477-481.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  46. Teather R. M., Wood P. J. Use of Congo red-polysaccharide interactions in enumeration and characterization of cellulolytic bacteria from the bovine rumen. Appl Environ Microbiol. 1982 Apr;43(4):777–780. doi: 10.1128/aem.43.4.777-780.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  47. Thakur I. S. Fractionation and analysis of allergenicity of allergens from Prosopis juliflora pollen. Int Arch Allergy Appl Immunol. 1989;90(2):124–129. doi: 10.1159/000235013. [DOI] [PubMed] [Google Scholar]
  48. Tsuboi A., Uchihi R., Tabata R., Takahashi Y., Hashiba H., Sasaki T., Yamagata H., Tsukagoshi N., Udaka S. Characterization of the genes coding for two major cell wall proteins from protein-producing Bacillus brevis 47: complete nucleotide sequence of the outer wall protein gene. J Bacteriol. 1986 Oct;168(1):365–373. doi: 10.1128/jb.168.1.365-373.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  49. Vellanoweth R. L., Rabinowitz J. C. The influence of ribosome-binding-site elements on translational efficiency in Bacillus subtilis and Escherichia coli in vivo. Mol Microbiol. 1992 May;6(9):1105–1114. doi: 10.1111/j.1365-2958.1992.tb01548.x. [DOI] [PubMed] [Google Scholar]
  50. Watson M. E. Compilation of published signal sequences. Nucleic Acids Res. 1984 Jul 11;12(13):5145–5164. doi: 10.1093/nar/12.13.5145. [DOI] [PMC free article] [PubMed] [Google Scholar]
  51. Wong K. K., Tan L. U., Saddler J. N. Multiplicity of beta-1,4-xylanase in microorganisms: functions and applications. Microbiol Rev. 1988 Sep;52(3):305–317. doi: 10.1128/mr.52.3.305-317.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  52. Yang R. C., Mackenzie C. R., Bilous D., Seligy V. L., Narang S. A. Molecular Cloning and Expression of a Xylanase Gene from Bacillus polymyxa in Escherichia coli. Appl Environ Microbiol. 1988 Apr;54(4):1023–1029. doi: 10.1128/aem.54.4.1023-1029.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  53. Zhang H., Scholl R., Browse J., Somerville C. Double stranded DNA sequencing as a choice for DNA sequencing. Nucleic Acids Res. 1988 Feb 11;16(3):1220–1220. doi: 10.1093/nar/16.3.1220. [DOI] [PMC free article] [PubMed] [Google Scholar]
  54. Zhang J. X., Flint H. J. A bifunctional xylanase encoded by the xynA gene of the rumen cellulolytic bacterium Ruminococcus flavefaciens 17 comprises two dissimilar domains linked by an asparagine/glutamine-rich sequence. Mol Microbiol. 1992 Apr;6(8):1013–1023. doi: 10.1111/j.1365-2958.1992.tb02167.x. [DOI] [PubMed] [Google Scholar]

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