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Genetics and Molecular Biology

Print version ISSN 1415-4757On-line version ISSN 1678-4685

Genet. Mol. Biol. vol.30 no.1 São Paulo  2007

https://doi.org/10.1590/S1415-47572007000100018 

GENETICS OF MICROORGANISMS
SHORT COMMUNICATION

 

Structural characterization of the bglH gene encoding a beta-glucosidase-like enzyme in an endophytic Bacillus pumilus strain

 

 

Andréa C. BogasI; Maria Angelica E. WatanabeI; Aneli BarbosaII; Laurival A. Vilas-BoasI; Ana C. BonattoIII; Robert DekkerII; Emanuel M. SouzaIII; Maria Helena P. FungaroI

ICentro de Ciências Biológicas, Universidade Estadual de Londrina, Londrina, PR, Brazil
IICentro de Ciências Exatas, Universidade Estadual de Londrina, Londrina, PR, Brazil
IIIDepartamento de Bioquímica e Biologia Molecular, Universidade Federal do Paraná, Curitiba, PR, Brazil

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ABSTRACT

A beta-glucosidase-like enzyme-encoding gene (bglH) of an endophytic Bacillus pumilus strain (CL16) was cloned using a shotgun genomic library constructed in Escherichia coli. The nucleotide sequence of the entire cloned fragment (2484 bp) was determined and characterized. An incomplete open reading frame (ORF) of 534 bp (ORF1) designated bglP and a complete ORF of 1419 bp (ORF2) designated bglH, located in the fragment, are organized in an operon. The protein deduced from 1419 bp (ORF2) had 472 amino acid residues without a characteristic signal peptide sequence, suggesting that the enzyme is localized in the cytoplasm. The amino acid sequence deduced from bglH gene had high similarity with b-glucosidases from the glycosyl hydrolase family 1. Over-expression of the B. pumilus bglH gene in E. coli showed a 54 kDa protein whose identity was confirmed by mass spectrometry (MALDI-TOF).

Key words: Bacillus pumilus, bglH, glucosidase, glycosyl hydrolase 1, PTS.


 

 

Cellulose comprises the major carbohydrate polymer of the plant cell wall. It is an unbranched polymer composed of anhydro-1,4-D-glucopyranoside units linked by b-glucosidic bonds. Enzymatic degradation of cellulose within the polysaccharide matrix of the cell wall requires the synergism of multiple enzymes such as the cellulases, exo- (cellobiohydrolase) and endo-b-1,4-glucanases, and b-glucosidases (cellobiases) (Knauf and Moniruzzaman, 2004). The b-glucosidases are widespread in microorganisms where they metabolize various carbohydrate substrates, including cellobiose, produced as a consequence of cellulose hydrolysis, and aromatic b-glucosides such as arbutin and salicin that are produced by a variety of plants (Tajima et al., 2001; Spiridonov and Wilson, 2001; Park et al., 2002; Marques et al., 2003; An et al., 2005).

Considerable polymorphism in b-glucosidase forms, functions and kinetics has been reported (Ogunseitan, 2003). Although several cellulolytic enzymes released by phytopathogens have already been well-characterized, knowledge on the uptake and hydrolysis of carbohydrates by endophytic microorganisms is limited. Endophyte microorganisms colonize inner plant tissues, living symbiotically with the host species (Azevedo et al., 2000). These microorganisms have been investigated as a source of new genes and proteins for use in industrial processes (Stamford et al., 2001, 2002; Pleban et al., 1997; Reddy et al., 1996; Moy et al., 2002; Lima et al., 2004).

Recently, 15 endophytic strains of Bacillus spp. isolated from Citrus were evaluated for cellulolytic activity (Lima et al., 2004). The Bacillus pumilus strain CL16 showed high cellulase activity and was selected for further studies. We have cloned the b-1,4-endoglucanase eglA gene from strain CL16 and expressed it in E. coli. The endo-1,4-b-glucanase EglA has high thermostability, an important feature in biotechnical processes that require high temperatures (Lima et al., 2004).

During the study described in the present paper we isolated and characterized a new locus of b-glucoside sugar utilization genes from the endophytic B. pumilus CL16 strain.

Using the degenerated primers DEG1F (5'-ATRACC TACTgNAARTTRgg-3') and DEG1R (5'gCRAANCCY AgHTARACggT-3') designed based on the amino acid regions conserved amongst b-glucosidases reported for Bacillus spp, a 560 bp B. pumilus fragment was obtained and successfully cloned in the pUC18 vector. Nucleotide sequence, determined using the DYEnamic ET DYE Terminator Cycle Sequencing Kit (Amersham Biosciences, Germany) on MegaBACE 1000 (Amersham Pharmacia Biotech, Germany), showed high similarity with the bglH gene from B. subtilis subsp. subtilis strain 168 (E value = 1e-17).

This fragment was successfully used as a probe for screening the bglH gene in a shotgun genomic library constructed from B. pumilus strain CL16 (Lima et al., 2004). Hybridization was done using the DIG High Prime DNA Labeling and Detection Starter Kit II, according to the manufacturer's instructions (Roche, Germany). Pre-hybridization (30 min) and hybridization (overnight) steps were at 42 ºC. Only one positive transformant was recovered from 2400 colonies. The recombinant plasmid isolated from this clone was denoted pMH2. The presence of the bglH gene was confirmed by two steps of sequencing. Firstly, using the M13 primers (Amersham Biosciences, Germany) and then with a set of new primers, GLICO1 F (5'-TCCAgAgATTCTTggACAAgT-3'), GLICO2 R (5'-CACTTggAACAAATTggTgATg-3') and GLm F (5'-gCATAAgCACggAATTgAgTC3-3') designed specifically for a bgl internal segment.

Two open reading frames (ORF) were found to compose the insert: an incomplete ORF of 534 bp (ORF1) and a complete one with 1419 bp (ORF2), which presented high similarity with the bglP and bglH genes, respectively, both from B. subtilis subsp. subtilis strain 168 (Kunst et al., 1997). The bglP gene from B. subtilis encodes an aryl-b-glucoside-specific enzyme II of the phosphoenolpyruvate sugar: phosphotransferase system (PTS), whereas the activity of BglH from B. subtilis was only recently directly demonstrated (Setlow et al., 2004). These authors showed that the bglH gene from B. subtilis encodes an aryl-phospho-b-D-glucosidase and that this gene was induced by aryl-b-D-glucosides.

The b-glucoside utilization pathways that rely upon the PTS for carbohydrate uptake have been characterized in several bacteria (Krüger and Hecker, 1995; Lai et al., 1997; Brown and Thomson, 1998; Brehm et al., 1999; Marasco et al., 1998; An et al., 2005), but not in B. pumilus. According to An et al. (2005) the discovery of new PTS-related sequences in bacterial genomes continues, and suggests that PTS enzymes might have additional unknown functions.

The nucleotide sequence of the entire insert (2484 bp) and the deduced protein sequence of the bglH gene from B. pumilus are shown in Figure 1. The ORF1 was upstream from ORF2, and separated by a 24 bp sequence. The absence of a promoter sequence between the ORFs identified by us, and their similarity with the operon described for B. subtilis strain 168 (Entrez Gene-NCBI server) suggest that they are organized into an operon. The nucleotide sequence downstream from ORF2 was compared to other sequences deposited at NCBI GenBank (BLASTX) but no similarity could be identified.

 

 

We found that the 1419-nucleotide-long ORF2 had a GC content of 41.6%. It was preceded by a potential ribosome binding site (AGGAGG) that was 9 bp upstream from the putative ATG start codon but, as expected, with no adjacent promoter sequence. Downstream from the TAA stop codon, no sequence resembling a rho-independent transcriptional terminator could be identified. The protein deduced from the ORF-complete sequence had 472 amino acid residues with an estimated molecular mass of 53.9 kDa and a isoelectric point of 4.97. The CDSearch program (NCBI server) revealed that BglH had a single domain consisting of the glycosyl hydrolase family 1 (GH1) sequence, covering 464 residues from amino acid 4 to 468.

The deduced B. pumilus BglH amino acid sequence was compared to other BglH sequences deposited at NCBI GenBank (Figure 2) and found to be highly similar to homologous enzymes from several Bacillus species: B. halodurans (gi 10173219), B. subtilis strain 168 (gi 7435440), B. cereus (gi 52144364), B. thuringiensis (gi 49477027), B. licheniformis (gi 52082495), B. clausii (gi 56965550). The Glu175 and Glu369 residues, the catalytic nucleophile, conserved in the B. pumilus BglH, are characteristic of family 1 proteins that hydrolyze glucosidic bonds by acid/base catalysis (Withers and Aebersold, 1995).

 

 

The absence of a signal peptide sequence (SignalP 3.0 program) and the lack of potential transmembrane regions (TMPred program) in the BglH sequence suggest that the enzyme is localized in the cytoplasm, as is the case for most bacterial b-glucosidases (Bhatia et al., 2002 and references therein).

We constructed an expression plasmid for the over-production of b-glucosidase (Bgl) by amplifying the bgl open reading frame (ORF) using the polymerase chain reaction (PCR) and the MHF (5'-CACCATgAACAAgTT AgAAAAAACAT-3') and MHR (5'-TTAgTAATCCAA ATgTTCCCCATTTg5-3') primer pair. For DNA polymerization the AccuPrime Pfx enzyme (Invitrogen, USA) was used. The amplified product was cloned into the pENTR/ SD/D-TOPO plasmid producing the entry vector of the Gateway Cloning System (Invitrogen, USA). From the entry vector the bgl gene was transferred to the expression vector pET-DEST42 by in vitro site-specific recombination. The recombinant expression plasmid containing the bgl gene was named the pAB1 plasmid. The cloned fragment was completely sequenced to confirm that no mutations were introduced during the amplification procedures.

Transformed Escherichia coli BL21 CodonPlus (DE3) cells harboring the pAB1 expression vector were grown on Luria-Bertani medium (LB) supplemented with 250 µg mL-1 ampicillin and incubated at 37ºC until the log phase (OD600nm = 0.2). After induction with 0.5 mmol L-1 IPTG (isopropyl-beta-D-thiogalactopyranoside) a strong band of 54 kDa was detected by sodium dodecyl sulfate polyacrylamide gel electrophoreses (SDS-PAGE) analysis (Laemmli, 1970), suggesting the over-expression of the B. pumilus bglH gene in E. coli (Figure 3). This molecular mass is consistent with that predicted from the amino acid sequence of the BglH protein. The over-expressed protein was completely purified and subjected to digestion with trypsin followed by peptide fingerprint analysis by matrix assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF/MS), in order to confirm the protein identity. The provided peptide masses were equivalent to the ones predicted, confirming that the over-expressed 54 kDa-band was in fact the BglH protein of B. pumilus.

 

 

Crude protein extracts obtained from the E. coli cells harboring the pAB1 plasmid were assayed for activity against r-nitrophenyl-b-D-glucopyranoside and cellobiose. Each assay consisted of 0.5 mL 5 mM of r-nitrophenyl-b-D-glucopyranoside or 0.2% of cellobiose as substrate, 0.1 mL of 50 mM phosphate buffer (pH 5.8 to 7.5) or Mc'Ilvaine buffer (pH 3 to 7) and 0.05 mL of crude enzyme. The mixture was incubated for 1 h at 37 ºC and the activity of b-glucosidase towards r-nitrophenyl-b-D-glucopyranoside was estimated by measuring the amount of r-nitrophenol released at 400 nm. The activity of b-glucosidase toward cellobiose was estimated by measuring the glucose released by the glucose oxidase method (Glucose Enzyme Color Kit, Bio Diagnostica, Brazil). The enzymatic activity of Bgl against r-nitrophenyl-b-D-glucopyranoside was assayed in Mc'Ilvaine buffer (pH 7.0) using the same protocol. Little activity against synthetic aryl-b-D-glucosides and no activity against cellobiose were observed. The highest activity against r-nitrophenyl-b-D-glucopyranoside (0.106 µmol min-1 mL-1) was observed using Mc'Ilvaine buffer at pH 7.0. This low activity was also observed using purified Bgl. The B. subtilis BglH also showed very low activity against non-phosphorylated b-glucosides. The enzyme activity against aryl-phospho-b-D-glucosides was not measured because there was no commercial supplier for this substrate.

 

Acknowledgments

We would like to thank Dr. Fábio de Oliveira Pedrosa (GENOPAR Consortium Coordinator) for providing us with laboratory facilities. This work was partially supported by the Brazilian agency Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq). A.C. Bogas is grateful to the Brazilian agency Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) for a scholarship.

 

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Send correspondence to:
MHP Fungaro
Departamento de Biologia Geral
Centro de Ciências Biológicas
Universidade Estadual de Londrina
Caixa Postal 6001, 86100-990 Londrina, PR, Brazil
E-mail: fungaro@uel.br

Received: November 28, 2005; Accepted: August 17, 2006.

 

 

Associate Editor: Luis Carlos de Souza Ferreira

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