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Previous Article | Next Article 
Applied and Environmental Microbiology, February 2005, p. 851-857, Vol. 71, No. 2
0099-2240/05/$08.00+0 doi:10.1128/AEM.71.2.851-857.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.
Karin Lanthaler,3
Geoff D. Robson,3
Jari Vehmaanperä,2,
Merja E. Penttilä,2 and
Christian P. Kubicek1
Research Area Gene Technology and Applied Biochemistry, Institute of Chemical Engineering, Vienna University of Technology, Vienna, Austria,1 VTT Biotechnology, Espoo, Finland,2 School of Biological Sciences, University of Manchester, Manchester, United Kingdom3
Received 28 May 2004/ Accepted 15 September 2004
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ABSTRACT |
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 Top Abstract IntroductionMaterials and MethodsResultsDiscussionReferences |
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bga1 strains grow more slowly and accumulate less biomass on lactose, but the cellobiohydrolase I and II gene expression and the final cellulase yields were comparable to those of the parental strain. Overexpression of bga1 under the control of the pyruvate kinase promoter reduced the lag phase, increased growth on lactose, and limited transcription of cellobiohydrolases. We detected an additional extracellular ß-galactosidase activity that was not encoded by bga1 but no intracellular ß-galactosidase activity. In conclusion, cellulase production on lactose occurs when ß-galactosidase activity levels are low but decreases as the ß-galactosidase activities increase. The data indicate that bga1-encoded ß-galactosidase activity is a critical factor for cellulase production on lactose. |
INTRODUCTION |
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TopAbstractIntroductionMaterials and MethodsResultsDiscussionReferences |
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A key enzyme in the induction of cellulase is galactokinase, since a galactokinase-negative mutant cannot induce cellulases during growth on lactose (30). Lactose can enter the cell after it is hydrolyzed extracellularly to D-glucose and D-galactose by a ß-galactosidase (lactase, ß-D-galactoside galactohydrolase; E.C 3.2.1.23), and the monosaccharides are then taken up by the respective permeases. Extracellular ß-galactosidases are known from several fungi, including Aspergillus niger, Aspergillus oryzae, and Penicillium canescens (5, 21, 26, 29). Alternatively, the lactose itself can be taken up by a specific lactose permease and hydrolyzed intracellularly. The latter mechanism has been demonstrated in the yeast Kluyveromyces lactis (6, 11), and Aspergillus nidulans is known to contain both an intracellular ß-galactosidase (12) and a lactose permease (L. Karaffa, B. Seiboth, and C. P. Kubicek, unpublished data). H. jecorina has been reported to have extracellular ß-galactosidase activity (25).
The objectives of the present work were to clone the bga1 gene encoding the extracellular ß-galactosidase of H. jecorina and to address the following questions. (i) Does H. jecorina contain other ß-galactosidases, in particular intracellular ß-galactosidases? (ii) Is the rate of extracellular lactose hydrolysis critical for induction of cellulases by lactose? And (iii) does manipulation of ß-galactosidase activity improve cellulase production on lactose? This information is needed to design and control industrial cellulase production with lactose as the carbon source.
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MATERIALS AND METHODS |
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TopAbstractIntroductionMaterials and MethodsResultsDiscussionReferences |
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For transcript analysis, strains were pregrown on glycerol (1%, wt/vol) for 20 h, mycelia were harvested by filtration and washed with tap water, equal amounts of mycelia were transferred to flasks containing the appropriate carbon source (1%, wt/vol), and cultivation was continued for 3 to 6 h. For lactose analysis, expression was analyzed without pregrowth on glycerol.
Escherichia coli strain NM538 (13) was used for library screening, and strains JM109 (Promega, Madison, Wis.) and XL1 Blue (Stratagene, La Jolla, Calif.) were used for plasmid propagation.
Fermentor cultivation.
The defined medium of Vogel (40) was used, except that lactose (10 g/liter) was used instead of sucrose as the carbon source and (NH4)2SO4 (1.65 g/liter) was used instead of NH4NO3 as the nitrogen source. Vogel's salts were prepared as a 50x solution and sterilized by membrane (pore size, 0.22 µm) filtration. The media for shake flask cultures contained Stabileze QM (methyl vinyl ether-maleic anhydride copolymer cross-linked with 1,9-decadien; ISP Technologies, Wayne, N.J.) or Junlon (18) to promote filamentous growth; the concentrations of Stabileze QM and Junlon used were 0.75 g/liter for cultures used for growth rate and enzyme determinations and 1.5 g/liter for precultures used for bioreactors. To prepare precultures, 40-ml batch cultures were grown in 250-ml Erlenmeyer flasks or 250-ml Nephlos flasks (36). The flasks were inoculated with 106 spores/ml (final concentration). The cultures were incubated on a rotary shaker at 200 rpm (throw, 2.5 cm) at 30°C. Fermentations were carried out in either an Applikon bioreactor (full working volume, 2.3 liters; FT Applikon Ltd., Tewkesbury, United Kingdom) or a B. Braun BIOSTAT M (full working volume, 2.1 liters; Sartorius BBI Systems, Melsungen, Germany) as previously described (42). The medium contained 10 g of lactose per liter as the sole carbon source. Cultures were inoculated with five 40-ml shake flask cultures which had been growing in medium containing 10 g of the same carbon source per liter for approximately 3 days. Fermentor cultures were maintained at 28 ± 1°C and pH 5.5 ± 0.1, agitated at 900 to 1,000 rpm with three six-blade (diameter, 48 mm) Rushton turbine impellers, and aerated with 0.7 liter of air liter of culture–1 min–1. Foaming was controlled by adding a mixture of polypropylene glycols (PPG) having different molecular weights that included PPG 1025 (BDH, VWR International, Poole, United Kingdom), PPG 2025 (BDH), and FoamMaster PPG (mixed molecular weight; Henkel Performance Chemicals, Leeds, United Kingdom) at a ratio of 2:2:1 (41), if necessary. For cultures grown in the BIOSTAT M, the PPG mixture was added as an aqueous suspension (25%, vol/vol), while for cultures grown in the Applikon bioreactor it was added as a 100% suspension.
Cloning and sequence analysis of bga1.
ß-Galactosidases from the following fungi and bacterium were used for an alignment to identify conserved regions: A. niger (GenBank accession no. P29853), A. oryzae (5), P. canescens (GenBank accession no. Q12660), and Bacillus circulans (GenBank accession no. JC5618). We used the degenerate primers 5'-GGCGGATCCCARAARTAYGTNACNTGGGAYGA-3' and 5'-GGCGGATCCTAYTCRTTYTCNRKYTG-3', corresponding to the amino acid sequences QKYVTWDD and Q(P/I)ENEY, with BamHI restriction sites (underlined) at their 5' ends for PCR amplification; QM9414 chromosomal DNA was used as the template. The following PCR cycling conditions were used: (i) 96°C for 10 min, after which 1 U of enzyme (Dynazyme II; Finnzymes, Espoo, Finland) per 100 µl of reaction mixture was added; (ii) 96°C for 4 min; (iii) three cycles consisting of 96°C for 1 min, 37 or 42°C for 30 s, and 72°C for 1 min; (iv) 24 cycles consisting of 96°C for 1 min, 55°C for 1 min, and 72°C for 1 min; and (v) 4°C indefinitely. PCR products (
500 bp) were isolated, cut with BamHI, and subcloned into similarly cleaved pBluescript SK(–) (Stratagene). The inserts were sequenced, and two identical clones (543 bp) with 76% amino acid identity to the ß-galactosidases of A. niger (accession no. P29853) and P. canescens (accession no. Q12660) were used as probes to screen a genomic EMBL3 
phage library (37) of QM9414. The bga1 gene was located on a 5-kb HindIII subclone, which was ligated into pUC18, resulting in pNS41. The 3' end of bga1 was located on a 2.8-kb XhoI-ClaI subclone, which was ligated to pBluescript SK(+), resulting in pBGAClaI. A bga1 cDNA fragment was cloned from a ZAP II library of H. jecorina RUT-C30 (33) and sequenced after in vivo excision into the phagemid vector pBluescript SK(–).
The genomic subclones and the deduced protein were analyzed with BLAST programs (1) and Expasy (http://www.expasy.org/). Consensus binding sequences in the bga1 5' region were identified manually.
Construction of plasmids for bga1 expression and deletion.
The upstream and downstream regions of the bga1 coding sequence were amplified by PCR that introduced an SmaI site between the two regions in which the A. nidulans amdS gene encoding acetamidase (19) was cloned. Thus, the 5' region was amplified from pNS41 by using oligonucleotides bGaldel1 (5'-GTCTCTTTCCCGGGTCCCAATTGGCCGTTTC-3') and M13forward, and the 3' region was amplified from pBGAClaI by using bGaldel2 (5'-CAATTGGGACCCGGGAAAGAGACTTGGGATTTTC-3') and M13reverse. Standard conditions were used for PCR. The resulting fragments were PstI/SmaI digested and ligated in the PstI-restricted vector pUC19-SmaI, resulting in pDBGA. pUC19-SmaI is identical to pUC19 (43) except that the SmaI site was eliminated by Acc65I and BamHI digestion. Finally, the 4-kb SalI-Acc65I amdS fragment of A. nidulans was blunted and ligated into the SmaI site of pDBGA, resulting in pDBGAamdS.
For bga1 overexpression, the coding region and 3' region were placed under the control of the pyruvate kinase promoter fragment in pRLMex30 (22). A 250-bp region of the N terminus of the bga1 gene coding region was amplified by PCR with bGalXbaI (5'-GTGATCTAGAACATGATGAGACCCGTCTC-3') and bGalHindIII (5'-TCTCAAGCTTGTGGAACACATCAAGATACAG-3'), and the amplicon was XbaI/HindIII digested and cloned into the respective sites of pRLMex30, resulting in pPKI-NBGA. Subsequently, a 4.8-kb ClaI-BglII bga1 fragment comprising the majority of the bga1 coding and terminator region was cloned into ClaI-HindIII-digested vector pPKI-NBGA, resulting in pPKI-BGA. The PCR-amplified portion of the sequence was verified by sequencing.
Construction of strains with altered bga1 expression.
H. jecorina was transformed as previously described (14). For bga1 gene replacement a 6.6-kb EcoRI fragment was excised from pDBGAamdS and purified from an agarose gel. Transformants were selected for growth on acetamide (10 mM) as the sole carbon source. Retransformation of a bga1 strain was done by cotransformation of a 6-kb HindIII-BglII bga1 fragment together with pRLMex30. Strains were selected for resistance to hygromycin (50 µg/ml). For bga1 amplification, strain TU-6 was cotransformed with plasmid pPKI-BGA and a 2.7-kb SalI pyr4 fragment of pFG1 (14).
Nucleic acid isolation and hybridization.
Total RNA was isolated as described by Chomczynski and Sacchi (7). Standard methods (3) were used for electrophoresis, blotting, and hybridization of nucleic acids. The probes used for hybridization were a 1.4-kb BglI cbh1 (cellobiohydrolase CBHI/Cel7A-encoding [32]) fragment, a 1.3-kb HaeII cbh2 (cellobiohydrolase CBHII/Cel6A-encoding [accession no. M55080]) fragment, a 1.9-kb Acc65I act1 (actin-encoding [accession no. X75421]) fragment, and the complete bga1 cDNA.
Preparation of cell extracts.
Cell extracts for enzyme activity assays were prepared from H. jecorina strains grown for 26 h on Mandels-Andreotti medium with the lactose or glycerol as the carbon source. The mycelia were harvested by filtration through Miracloth (Calbiochem, VWR International, Vienna, Austria), washed with cold sterile tap water, blotted dry with paper towels, and ground to a fine powder under liquid N2 in a mortar and pestle. One gram (wet weight) of ground mycelium was mixed with 3 ml of extraction buffer (0.1 M Tris-HCl [pH 7.5], 1 mM EDTA, 5 mM ß-mercaptoethanol), suspended, and homogenized by sonication 10 times for 30 s at 2°C, with intermittent 2-min cooling periods. The resulting homogenate was centrifuged at 10,000 x g for 20 min at 4°C. The supernatant (average protein concentration, 8 to 15 mg/ml) was used as a cell extract for measuring intracellular ß-galactosidase activity. After repeated washing of the remaining pellet with 0.1% Triton X-100, the cell debris was resuspended in 3 ml of citrate buffer (pH 5) per g (dry weight) of the original mycelium and was used as a source to measure cell wall-bound ß-galactosidase activity.
Enzyme assay.
ß-Galactosidase activity was determined with o-nitrophenyl-ß-D-galactopyranoside as the substrate. Cell extracts, supernatant, and cell wall-bound samples were diluted to 700 µl with 0.1 M phosphate buffer (pH 5 or 7) and added to 300 µl of 10 mM o-nitrophenyl-ß-D-galactopyranoside. After incubation for 10 to 60 min at 30°C, the reaction was stopped by addition of 3 ml of 1 M Na2CO3. Assay mixtures containing cell wall samples were centrifuged (10,000 x g for 10 min at room temperature) before measurement. The A405 was measured against a blank when the reaction had been stopped at zero time. Enzyme activities were expressed in units, and 1 U corresponded to the conversion of 10 µmol of substrate per min under the conditions used.
ß-Glucosidase and cellulase activities were assayed as described previously (39). Culture supernatant was filtered through 0.22-µm-pore-size filters (Millipore GesmbH, Vienna, Austria), and aliquots were stored at –20°C for subsequent analysis. Total cellulase activity was determined by using p-nitrophenyl-ß-D-lactopyranoside instead of 4-methylumbelliferyl-ß-D-lactoside. Briefly, p-nitrophenyl-ß-D-lactopyranoside (400 µl; 1 mg/ml in 50 mM citric acid buffer [pH 5.0]) was incubated with 50 µl of culture supernatant (diluted as necessary) or a standard (500 to 10 mg/liter) in an Eppendorf tube for 1 h at 37°C, and the reaction was terminated by adding 500 µl of 0.1 M borax. The p-nitrophenyl released during the reaction was measured by determining changes in the A405.
ß-Glucosidase activity was measured by using the protocol described above, except that p-nitrophenyl-ß-D-glucopyranoside was used as the substrate (20).
Determination of fungal growth and biomass.
To determine hyphal growth on agar plates, plates were inoculated with a small piece of agar in the center of each 11-cm plate. The biomass in submerged cultures was measured by filtering two 10-ml portions of culture onto predried and preweighed Whatman no. 1 filter papers. The harvested biomass was dried to constant weight (70°C for at least 3 days or 30 min in a microwave oven at 260 W), after each filter was washed with at least 20 ml of deionized water.
Growth rates in bioreactors were estimated from the CO2 output by using an ADC 7000 infrared gas analyzer (The Analytical Development Co. Ltd., Hoddesdon, United Kingdom).
Biochemical analyses.
Protein concentrations were determined by the Bio-Rad protein assay (Bio-Rad Laboratories, Munich, Germany). The protocols described by Ausubel et al. (3) were used for sodium dodecyl sulfate-polyacrylamide gel electrophoresis (with 10% polyacrylamide gels) and Western blotting. Monoclonal antibodies were used to detect cellobiohydrolases CBHI/Cel7A and CBHII/Cel6A (24).
Nucleotide sequence accession number.
The bga1 sequence has been deposited in the GenBank database under accession number AJ549427.
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RESULTS |
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A sequence analysis of 1 kb of the bga1 promoter region resulted in identification of a number of consensus binding sites for fungal transcription factors (Fig. 1), including six sites for the CCAAT-binding Hap2/3/5 complex (44), three single sites and one double site for the carbon catabolite repressor Cre1 (SYRGGRG) (17, 34), and one site each for the cellulase and xylanase repressor Ace1 (AGGCA) (2) and the transcriptional activator AmyR (CGGN8CGG) (35). No consensus binding sites for XlnR, the A. niger transcriptional activator of xylanase and cellulase biosynthesis (38) which is also involved in regulation of A. niger lacA (8), or for Saccharomyces cerevisiae Gal4 (CGGN11CCG) (10), the transcriptional activator of the Leloir pathway genes, were found.
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bga1 strains, confirming its deletion. On agar plates, the bga1 deletion strains grew at the wild-type rate with D-galactose as the carbon source but at lower rates with lactose or D-glucose. The effect observed with D-glucose was not due to ectopic insertion of the transforming DNA at other loci because the wild-type phenotype could be completely restored by retransformation of the bga1 deletion strains with the bga1 gene (data not shown).
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bga1 strains in shake flasks and monitored the increase in biomass (Fig. 3B). In the presence of peptone, growth of the bga1 strain started at the same time (10 to 15 h after inoculation), and the growth rate was approximately constant throughout the incubation experiment. However, the biomass concentration of the bga1 strain was somewhat less than one-half of the biomass concentration of the parent strain (2.3 versus 6.0 g/liter). The two strains also were grown in the absence of peptone in controlled fermentor cultures. In this case, the loss of function of bga1 was dramatic and resulted in a significantly delayed onset of growth on lactose (125 versus 40 h). The final decrease in biomass yield (2.5 versus 4.8 g/liter) was comparable to that in shake flasks, however.
Activity of Bga1.
We compared the ß-galactosidase activities in the culture supernatant, cell extract, and mycelial debris after homogenization of QM9414 and the bga1 strain after growth for 24 h on lactose. More than 95% of the total extracellular ß-galactosidase activity of QM9414 was secreted into the culture supernatant, while only a small percentage was associated with the cell walls (0.86 versus 0.006 U/g [dry weight] of mycelium). Most of the activity present in the culture medium was lost in the bga1 mutant (0.07 U/g [dry weight] of mycelium), indicating that H. jecorina has a second ß-galactosidase which accounts for 10% of the total extracellular ß-galactosidase activity hydrolyzing aryl-ß-galactoside. No intracellular ß-galactosidase activity was detected during growth on lactose at either pH 5.0 or pH 7.0.
Lactose-dependent induction of cellulase gene expression in the bga1 strain.
We cultivated QM9414 and the bga1 strain on lactose and measured the total cellulase and ß-glucosidase activities and the accumulation of the cellobiohydrolase CBHI/Cel7A protein in the supernatant. The appearance of cellulase and ß-glucosidase activities in the medium was delayed in the bga1 mutant, but the final levels were comparable when they were related to the biomass of the parent strain. Consistent with these data, the level of the CBHI/Cel7A protein that accumulated was only about one-half of the wild-type level in the bga1 strain. These findings suggested that loss of the bga1-encoded ß-galactosidase function does not have a major effect on cellulase gene expression. We measured the accumulation of the transcripts of two major cellulase genes, cbh1 and cbh2, in both strains (Fig. 3C). The levels of both cellulase transcripts that accumulated were about the same in the two strains, except at 24 h, when the cbh1 and cbh2 transcript levels were lower in bga1. This difference could have been due to slower growth by the bga1 strain on lactose. Thus, the induction of both genes—apart from some growth-related retardation—was not affected in the bga1 deletion strain.
Overexpression of bga1 and cellulase formation.
We constructed a series of H. jecorina strains that expressed bga1 under the expression signals of the H. jecorina pki1 (pyruvate kinase-encoding gene) promoter region and the bga1 terminator region and compared their ß-galactosidase activities after 24 h of growth on glycerol. The different transformants produced between 3 and 18 U/g (dry weight). Therefore, the best overexpressing transformants had up to >30-fold-greater ß-galactosidase activity than lactose-grown cultures of QM9414. Three of these transformants (PKI-BGA3, PKI-BGA7, and PKI-BGA13), which secreted different ß-galactosidase activities (3, 5, and 12 U/g [dry weight], respectively), were grown on lactose in shake flasks and evaluated for cellulase formation and cellulase gene transcription. All three transformants had a significantly higher rate of growth on lactose plus peptone (0.27 to 0.29 g [dry weight]/h) and reached the final dry weight (6.4 g/liter) after 50 h of cultivation (Fig. 4A). All three transformants also had lost the ability to induce cbh1 and cbh2 gene expression on lactose as a carbon source (Fig. 4B), although we observed induction on cellulose in a manner and at a level comparable to the manner and level in the parental strain (data not shown). We also grew strain PKI-BGA13 in the fermentor in the absence of peptone and observed similar results (i.e., a reduced initial lag phase and 24-h-earlier production of the maximal amount of biomass).
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DISCUSSION |
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TopAbstractIntroductionMaterials and MethodsResultsDiscussionReferences |
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No intracellular ß-galactosidase activity was found. The intracellular ß-galactosidases of fungi are rather stable enzymes (12), and we have been able to extract a number of other more labile enzymes in active forms from H. jecorina without having to use protease inhibitors by the same method (e.g., oxidoreductases involved in D-xylose and L-arabinose metabolism). It is therefore unlikely that the lack of an intracellular ß-galactosidase is due to proteolytic or other inactivation during extraction.
This finding is consistent with results of a TBLASTN search (Expect, 1e–5) of the H. jecorina genome database with the intracellular ß-galactosidase of K. lactis (accession no. P00723), a family 2 glycosyl hydrolase, as the query, which produced no hits. In contrast, the genomes of A. nidulans and N. crassa (http://www.broad.mit.edu/annotation/fungi/) each contain two putative family 2 ß-galactosidases (accession no. AN3201.2, AN2463.2, NCU05956.1, and NCU00810.1).
The lack of an intracellular ß-galactosidase in H. jecorina implies that lactose is hydrolyzed extracellularly. This conclusion is consistent with the preliminary finding that germinated spores of H. jecorina grown on lactose can take up D-glucose and D-galactose (the hydrolysis products of lactose) but not lactose (Vehmaanperä, unpublished data). However, genes encoding putative orthologs of the lactose permeases of K. lactis (accession no. P07921) are found in the genome databases of fungi, including T. reesei (E value, 5e–84), A. nidulans (E value, 2e–81), and N. crassa (E value, 2e–79). Thus, it will be interesting to see whether this gene is expressed during growth on lactose in H. jecorina and whether its gene product catalyzes the transport of lactose.
Genetic manipulation of Bga1 activity by deletion or overexpression perceptibly affects growth on lactose during the early stages of cultivation. This effect is even more dramatic in the bga1 strain in the absence of peptone; however, there is no obvious correlation between changes in Bga1 activity and the growth rate on lactose. Reduction of the ß-galactosidase activity by 90% only halved the growth rate, while a >10-fold increase in activity only tripled it.
These results suggest the presence of additional ß-galactosidases which either do not hydrolyze aryl-ß-galactosides or have only very low activity with them. The residual 5% of ß-galactosidase activity found in the bga1 strain could result from a second ß-galactosidase. A putative candidate was found in the T. reesei genome database (accession no. fg.V.1.C3000108), and this candidate showed a reasonable degree of identity to a ß-galactosidase of Bacteroides thetaiotaomicron (accession no. AAO78619.1; E value, 1e–67) and in addition contained a signal peptide at its N terminus. An additional hit for a ß-galactosidase was obtained in a TBLASTN search, but the nucleotide sequence of this contig was 100% identical to the DNA sequence of the Haemophilus somnus ß-galactosidase/ß-glucuronidase (accession no. ZP_00122729) and occurred on a very small contig. Therefore, we considered this match to be an artifact. Presumably, this second ß-galactosidase has an unusual amino acid sequence, or its activity is a secondary activity of another glycosidase.
The occurrence of a ß-galactosidase in a saprophytic ascomycete like H. jecorina is somewhat paradoxical, as lactose does not occur in its natural environment, and the induction caused by lactose may be artificial. It is more likely that plant polysaccharides containing ß-galactosidic linkages are the true substrates for the ß-galactosidase. These polysaccharides also may contain L-arabinose, since bga1 expression was triggered by both D-galactose and L-arabinose. In A. niger the extracellular ß-galactosidase-encoding gene lacA was shown to be induced by the plant cell wall heteropolysaccharide pectin and several pectin monomers, including D-galacturonic acid, L-arabinose, and D-galactose, indicating that it may be involved in pectin degradation (9).
Overexpression of the bga1 gene product, but not its deletion, eliminated cellulase gene expression on lactose. This result suggests that increased ß-galactosidase activity interferes with cellulase induction. One simple explanation for this finding is that the ß-galactosidase activity eliminates the inducer. However, we have no evidence that lactose is the inducer, and the lack of intracellular ß-galactosidase activity, which is necessary for intracellular lactose catabolism and the termination of induction, argues against this possibility. Alternatively, increased concentrations of lactose hydrolysis products (i.e., D-glucose and D-galactose), which accumulate in the medium, could result in catabolite repression of cellulase gene expression. However, the carbon catabolite repression of cbh1 and other cellulase genes is only partial (45), and carbon catabolite repression alone should not result in a complete loss of cbh1 gene transcription, like that seen in the bga1-overexpressing mutants. Also, growing the H. jecorina cre1 loss-of-function strain RUT-C30 in the simultaneous presence of equimolar concentrations of D-glucose and D-galactose (S. Gyamphi and C. P. Kubicek, unpublished data) or D-galactose alone (30) does not result in cellulase production, which makes Cre1-dependent carbon catabolite repression a less likely explanation.
Another possible explanation is that D-galactose uptake could be inhibited by D-glucose. H. jecorina transports D-galactose with a general hexose transporter that can be inhibited by an excess of other hexoses (e.g., D-glucose and D-mannose) (Vehmaanperä, unpublished). However, D-glucose and D-galactose are present in the medium at comparable concentrations, and the affinities of the transporter for them are in the same concentration range, so a complete block of D-galactose uptake by D-glucose uptake is unlikely.
We recently showed that eliminating the galactokinase step in the Leloir pathway also eliminates cellulase induction by lactose, although growth on lactose still occurs (30). We interpreted these results to mean that either D-galactose, bound to galactokinase, or D-galactose-1-phosphate was the inducer of cellulase formation on lactose. We also suggested that this induction occurred only at a narrow range of concentrations of either of these intermediates, because D-galactose itself does not induce cellulase gene expression, even in a Cre1-negative background. This model is also consistent with the present data if the overexpression of bga1 influences the intracellular steady-state levels of either D-galactose or D-galactose-1-phosphate, which leads to a shutdown of cellulose transcription. Although the Leloir pathway genes of H. jecorina are not subject to glucose repression (30, 31), which may take place because of the increased rate of lactose hydrolysis, competition for substrates and coenzymes (e.g., ATP) may occur.
The data presented in this paper show that the H. jecorina bga1-encoded ß-galactosidase activity has a major impact on the growth rate during lactose-based fermentations and on the performance of cellulase formation by H. jecorina in this process. Consequently, further attempts to manipulate the expression of genes involved in this process are needed to improve the production rate and yield of mutant strains on an industrial scale.
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ACKNOWLEDGMENTS |
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We thank Arja Mäntylä for useful discussions.
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FOOTNOTES |
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Present address: BioTie Therapies, FIN-00790 Helsinki, Finland.
Present address: Roal Oy, FIN-05201 Rajamäki, Finland.
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REFERENCES |
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TopAbstractIntroductionMaterials and MethodsResultsDiscussionReferences |
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-galactosidase genes and a single ß-galactosidase gene from Aspergillus niger. Appl. Environ. Microbiol. 65:2453-2460. replacement vectors carrying polylinker sequences. J. Mol. Biol. 170:827-842.[Medline]
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, Cre1; 
, Hap2/3/5; 
, Ace1; 
, AmyR; 
, Msn2/4.
) and strain 
) in shake flasks with peptone (0.1%, wt/vol) and lactose (1%, wt/vol) as carbon sources. The error bars indicate standard deviations for three different experiments. (C) Northern analysis of cbh1 and cbh2 transcript levels during growth on lactose. 18S RNA served as a loading control.
) on lactose in shake flasks. The error bars indicate standard deviations for three different experiments. (B) Effect of bga1 overexpression on cbh1 and cbh2 accumulation during growth on lactose.