Skip to main content
Log in

DNA sequence and transcription of an endoglucanase gene fromPrevotella (Bacteroides) ruminicola AR20

  • Published:
Molecular and General Genetics MGG Aims and scope Submit manuscript

Summary

The endoglucanase gene was sequenced fromPrevotella ruminicola AR20, isolated as clone pJW4. The endoglucanase (BrEND) is encoded by an open reading frame (ORF1) of 501 codons, corresponding to a protein of calculated molecular weight 55.7 kDa. Analysis of proteins on SDS-PAGE revealed a protein corresponding to the calculated molecular weight of the processed BrEND. The protein showed substantial homology to members of the A4 sub-family cellulases. Primer extension studies revealed that transcription ofcelA is initiated at different sites inEscherichia coli andPrevotella ruminicola. E. coli σ70 recognition sequences were identified, which were located upstream from the transcription initiation site (TIS) functional inE. coli. A longer extension product was identified using RNA fromP. ruminicola, indicating that the gene may normally be transcribed as part of a polycistronic message. The end of the primer extension product corresponded to a site beyond the 5′ boundary of the cloned fragment, thus preventing identification of native promoter sequences. A second ORF of 110 codons (ORF2) was identified on the antisense strand, and primer extension indicated that transcription through ORF2 was initiated at an identical site in bothE. coli andP. ruminicola. E. coli-like consensus sequences were located at positions −10 and −35 upstream from this site, suggesting that some promoter sequences inP. ruminicola are similar toE. coli consensus sequences, although others recognized byE. coli are non-functional inP. ruminicola. The presence of a strong potential ribosome-binding site at nucleotide positions 25–38 of the antisense transcript could indicate that ORF2 is translated inP. ruminicola; however, a protein corresponding to this ORF was not detected on SDS-PAGE. This suggests that it is more likely that ribosomal binding of the antisense transcript plays a part in translational regulation of endoglucanase expression.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Asmundson RV, Huang C-M, Kelly WJ, Yu P-L, Curry MM (1990) The cellulase ofRuminococcus flavefaciens strain 186: characterization, cloning and use in ruminant nutrition In: Akin DE, Ljungdahl LG, Wilson JR, Harris PJ (eds) Microbial and plant opportunities to improve lignocellulose utilization by ruminants. Elsevier, New York, pp 401–409

    Google Scholar 

  • Béguin P (1990) Molecular biology of cellulose degradation. Annu Rev Microbiol 44:219–248

    Google Scholar 

  • Berger E, Jones WA, Jones DT, Woods DR (1989) Cloning and sequencing of an endoglucanase (end1) gene fromButyrivibrio fibrisolvens H17c. Mol Gen Genet 219:193–198

    Google Scholar 

  • Berger E, Jones WA, Jones DT, Woods DR (1990) Sequencing and expression of a cellodextrinase (ced1) gene fromButyrivibrio fibrisolvens H17c cloned inEscherichia coli. Mol Gen Genet 223:310–318

    Google Scholar 

  • Brosius J (1984) Plasmid vectors for the selection of promoters. Gene 27:151–160

    Google Scholar 

  • Cavicchioli R, Watson K (1991) The involvement of transcriptional read-through from internal promoters in the expression of a novel endoglucanase gene inFibrobacter succinogenes AR1. Nucleic Acids Res 19:1661–1669

    Google Scholar 

  • Cavicchioli R, East PD, Watson K (1991)endA FS, a novel family E endoglucanase gene fromFibrobacter succinogenes. J Bacteriol 173:3265–3268

    Google Scholar 

  • Chomczynski P, Sacchi N (1987) Single step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction. Anal Biochem 162:156–159

    Google Scholar 

  • Devereux J, Haeberli P, Smithies O (1984) A comprehensive set of sequence analysis programs for the VAX. Nucleic Acids Res 12:387–395

    Google Scholar 

  • Dower WJ, Miller JF, Ragsdale CW (1988) High efficiency transformation ofE. coli by high voltage electroporation. Nucleic Acids Res 16:6127–6145

    Google Scholar 

  • Flint HJ, Thomson AM (1991) The genetic manipulation of rumen bacteria with special reference to fibre digestion. Anim Feed Sci Technol 32:123–129

    Google Scholar 

  • Fukumori F, Ohishi K, Kudo T, Horikoshi K (1987) Tandem location of the cellulase genes on the chromosome ofBacillus sp. strain N-4. FEMS Microbiol Lett 48:65–68

    Google Scholar 

  • Gibson TJ (1984) Studies on the Epstein-Bar virus genome. PhD Thesis, Cambridge University, UK

    Google Scholar 

  • Gierasch LM (1989) Signal sequences. Biochemistry 28:923–929

    Google Scholar 

  • Green PJ, Pines O, Inouye M (1986) The role of antisense RNA in gene regulation. Annu Rev Biochem 55:569–597

    Google Scholar 

  • Gregg K (1989) Genetic engineering of rumen bacteria. In: Rogers GE, Reis PJ, Ward KA, Marshall RC (eds) The biology of wool and hair. Chapman and Hall, London, pp 417–424

    Google Scholar 

  • Hall J, Hazlewood GP, Barker PJ, Gilbert HJ (1988) Conserved reiterated domains inClostridium thermocellum endoglucanases are not essential for catalytic activity. Gene 69:29–38

    Google Scholar 

  • Hall J, Hazlewood GP, Huskisson NS, Durrant AJ, Gilbert HJ (1989) Conserved serine-rich sequences in xylanase and cellulase fromPseudomonas fuorescens subspeciescellulosa: internal signal sequence and unusual protein processing. Mol Microbiol 3:1211–1219

    Google Scholar 

  • Hanahan D (1985) Techniques for transformation ofE. coli. In: DNA cloning: A practical approach, vol 1, pp 109–135

    Google Scholar 

  • Hawley DK, McClure WR (1983) Compilation and analysis ofEscherichia coli promoter DNA sequences. Nucleic Acids Res 11:2237–2255

    Google Scholar 

  • Hazlewood GP, Davidson K, Laurie JI, Romaniec MPM, Gilbert HJ (1990) Cloning and sequencing of thecelA gene encoding endoglucanase A ofButyrivibrio fibrisolvens strain A46. J Gen Microbiol 136:2089–2097

    Google Scholar 

  • Henrissat B, Claeyssens M, Tomme P, Lemesle L, Mornon J-P (1989) Cellulase families revealed by hydrophobic cluster analysis. Gene 81:83–95

    Google Scholar 

  • Higgins DG, Sharp PM (1988) CLUSTAL: a package for performing multiple sequence alignment on a microcomputer. Gene 73:237–244

    Google Scholar 

  • Janssen PJ, Jones DT, Woods DR (1990) Studies onClostridium acetobutylicum glnA promoters and antisense RNA. Mol Microbiol 4:1575–1583

    Google Scholar 

  • Kellett LE, Poole DM, Ferreira LMA, Durrant AJ, Hazlewood GP, Gilbert HJ (1990) Xylanase B and an arabinofuranoside fromPseudomonas fluorescens subsp.cellulosa contain identical cellulose-binding domains and are encoded by adjacent genes. Biochem J 272:369–376

    Google Scholar 

  • Laemmli UK (1970) Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 227:680–685

    Google Scholar 

  • Lin L-L, Rumbak E, Zappa H, Thomson JA, Woods DR (1990) Cloning, sequencing and analysis of expression of aButyrivibrio fibrisolvens gene encoding a β-glucosidase. J Gen Microbiol 136:1567–1576

    Google Scholar 

  • Maniatis T, Fritsch EF, Sambrook J (1982) Molecular cloning: A laboratory manual. Cold Spring Harbour Laboratory, Cold Spring Harbour, NY

    Google Scholar 

  • Matsushita O, Russell JB, Wilson DB (1990) Cloning and sequencing of aBacteroides ruminicola B14 endoglucanase gene. J Bacteriol 172:3620–3630

    Google Scholar 

  • Matsushita O, Russell JB, Wilson DB (1991) ABacteroides ruminicola 1,4,-β-D-endoglucanase is encoded in two reading frames. J Bacteriol 173:6919–6926

    Google Scholar 

  • McGavin MJ, Forsberg CW, Crosby B, Bell AW, Dignard D, Thomas DY (1989) Structure of thecel-3 gene fromFibrobacter succinogenes S85 and characteristics of the encoded gene product, endoglucanase 3. J Bacteriol 171:5587–5595

    Google Scholar 

  • Mead DA, Szczesna-Skorupa E, Kemper B (1986) Single-stranded DNA ‘blue’ T7 promoter plasmids: a versatile tandem promoter system for cloning and protein engineering. Protein Engineering 1:67–74

    Google Scholar 

  • Moser B, Gilkes NR, Kilburn DG, Warren RAJ, Miller RC Jr (1989) Purification and characterization of endoglucanase C ofCellulomonas fimi, cloning of the gene, and analysis of in vivo transcripts of the gene. Appl Environ Microbiol 55:2480–2487

    Google Scholar 

  • Ohmiya K, Kajino T, Kato A, Shimizu S (1989) Structure of aRuminococcus albus endo-1,4-β-glucanase gene. J Bacteriol 171:6771–6775

    Google Scholar 

  • Ohmiya K, Takano M, Shimizu S (1990) DNA sequence of a β-glucosidase fromRuminococcus albus. Nucleic Acids Res 16:671

    Google Scholar 

  • Poole DM, Hazlewood GP, Laurie JI, Barker PJ, Gilbert HJ (1990) Nucleotide sequence of theRuminococcus albus SY3 endoglucanase genescelA andcelB. Mol Gen Genet 223:217–223

    Google Scholar 

  • Raleigh EA, Murray NE, Revel H, Blumenthal RM, Westaway AD, Rigby PWJ, Elhai J, Hanahan D (1988) McrA, McrB restriction phenotypes of someE. coli strains and implications for gene cloning. Nucleic Acids Res 16:1563–1575

    Google Scholar 

  • Russell JB, Wilson DB (1988) Potential opportunities and problems for genetically altered rumen microorganisms. J Nutr 118:271–279

    Google Scholar 

  • Sanger F, Nicklen S, Coulsen AR (1977) DNA sequencing with chain terminating inhibitors. Proc Natl Acad Sci USA 74:5463–5467

    Google Scholar 

  • Schwarz WH, Schimming S, Staudenbauer WL (1988) Isolation of aClostridium thermocellum gene encoding a thermostable β-1,3-glucanase (laminarinase). Biotechnol Lett 10:225–230

    Google Scholar 

  • Shah HN, Collins MD (1990)Prevotella, a new genus to includeBacteroides melaninogenicus and related species formerly classified in the genusBacteroides. Int J Syst Bacteriol 40:205–208

    Google Scholar 

  • Shine J, Dalgarno L (1974) The 3′ terminal sequence ofEscherichia coli 16S ribosomal RNA: complementarity to nonsense triplets and ribosome binding sites. Proc Natl Acad Sci USA 71:1342–1346

    Google Scholar 

  • Teather RM (1985) Application of gene manipulation to rumen microflora. Can J Anim Sci 65:563–574

    Google Scholar 

  • Teather RM (1990) Structure of β-glucanase genes from rumen bacteria. In: Akin DE, Ljungdahl LG, Wilson JR, Harris PJ (eds) Microbial and plant opportunities to improve lignocellulose utilization by ruminants. Elsevier, New York, pp 377–388

    Google Scholar 

  • Teather RM, Erfle JD (1990) DNA sequence of aFibrobacter succinogenes mixed linkage β-glucanase (1,3-1,4-β-D-glucan 4-glucanohydrolase) gene. J Bacteriol 172:3837–3841

    Google Scholar 

  • Utt EA, Eddy CK, Keshav KF, Ingram LO (1991) Sequencing and expression of theButyrivibrio fibrisolvens xylB gene encoding a novel bifunctional protein with β-D-xylosidase and α-L-arabi-nofuranosidase activities. Appl Environ Microbiol 57:1227–1234

    Google Scholar 

  • Wang W, Thomson JA (1990) Nucleotide sequence of thecelA gene encoding a cellodextrinase ofRuminococcus flavefaciens FD-1. Mol Gen Genet 222:265–269

    Google Scholar 

  • Watson MEE (1984) Compilation of published signal sequences. Nucleic Acids Res 12:5145–5164

    Google Scholar 

  • Weisburg WG, Oyaizu Y, Oyaizu H, Woese CR (1985) Natural relationship betweenBacteroides andFlavobacter. J Bacteriol 164:230–236

    Google Scholar 

  • Whitehead TR, Hespell RB (1990) The genes for three xylandegrading activities fromBacteroides ovatus are clustered in a 3.8-kilobase region. J Bacteriol 172:2408–2412

    Google Scholar 

  • Woods JR, Hudman F, Gregg K (1989) Isolation of an endoglucanase gene fromBacteroides ruminicola subsp.brevis. J Gen Microbiol 135:2543–2549

    Google Scholar 

  • Wynne EC, Pemberton JM (1986) Cloning of a gene cluster fromCellvibrio mixtus which codes for cellulose, chitinase, amylase, and pectinase. Appl Environ Microbiol 52:1362–1367

    Google Scholar 

  • Yanisch-Perron C, Vieira J, Messing J (1985) Improving M13 phage cloning vectors and host strains: nucleotide sequences of the M13mp18 and pUC19 vectors. Gene 33:103–119

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Vercoe, P.E., Gregg, K. DNA sequence and transcription of an endoglucanase gene fromPrevotella (Bacteroides) ruminicola AR20. Molec. Gen. Genet. 233, 284–292 (1992). https://doi.org/10.1007/BF00587590

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00587590

Key words

Navigation