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This article is part of the series Systems biotechnology and metabolic engineering.

Open Access Research

Improved production of secreted heterologous enzyme in Bacillus subtilis strain MGB874 via modification of glutamate metabolism and growth conditions

Kenji Manabe12, Yasushi Kageyama1, Takuya Morimoto1, Eri Shimizu3, Hiroki Takahashi4, Shigehiko Kanaya5, Katsutoshi Ara6, Katsuya Ozaki1* and Naotake Ogasawara2*

Author Affiliations

1 Biological Science Laboratories, Kao Corporation, 2606 Akabane, Ichikai, Haga, Tochigi 321-3497, Japan

2 Graduate School of Biological Science, Nara Institute of Science and Technology, 8916-5 Takayama, Ikoma, Nara 630-0101, Japan

3 Analytical Science Laboratories, Kao Corporation, 2606 Akabane, Ichikai, Haga, Tochigi 321-3497, Japan

4 Medical Mycology Research Center, Chiba University, 1-8-1 Inohana, Chuo-ku, Chiba 260-8673, Japan

5 Graduate School of Information Science, Nara Institute of Science and Technology, 8916-5 Takayama, Ikoma, Nara 630-0101, Japan

6 Fundamental Technology Research Laboratories, Kao Corporation, 623 Zi Ri Rd, Minhang Dist, Shanghai 200241, China

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Microbial Cell Factories 2013, 12:18  doi:10.1186/1475-2859-12-18

The electronic version of this article is the complete one and can be found online at: http://www.microbialcellfactories.com/content/12/1/18


Received:9 December 2012
Accepted:6 February 2013
Published:18 February 2013

© 2013 Manabe et al; licensee BioMed Central Ltd.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Background

The Bacillus subtilis genome-reduced strain MGB874 exhibits enhanced production of exogenous extracellular enzymes under batch fermentation conditions. We predicted that deletion of the gene for RocG, a bi-functional protein that acts as a glutamate dehydrogenase and an indirect repressor of glutamate synthesis, would improve glutamate metabolism, leading to further increased enzyme production. However, deletion of rocG dramatically decreased production of the alkaline cellulase Egl-237 in strain MGB874 (strain 874∆rocG).

Results

Transcriptome analysis and cultivation profiles suggest that this phenomenon is attributable to impaired secretion of alkaline cellulase Egl-237 and nitrogen starvation, caused by decreased external pH and ammonium depletion, respectively. With NH3-pH auxostat fermentation, production of alkaline cellulase Egl-237 in strain 874∆rocG was increased, exceeding that in the wild-type-background strain 168∆rocG. Notably, in strain 874∆rocG, high enzyme productivity was observed throughout cultivation, possibly due to enhancement of metabolic flux from 2-oxoglutarate to glutamate and generation of metabolic energy through activation of the tricarboxylic acid (TCA) cycle. The level of alkaline cellulase Egl-237 obtained corresponded to about 5.5 g l-1, the highest level reported so far.

Conclusions

We found the highest levels of production of alkaline cellulase Egl-237 with the reduced-genome strain 874∆rocG and using the NH3-pH auxostat. Deletion of the glutamate dehydrogenase gene rocG enhanced enzyme production via a prolonged auxostat fermentation, possibly due to improved glutamate synthesis and enhanced generation of metabolism energy.

Keywords:
Bacillus subtilis; Protein secretion; Genome reduction; Glutamate metabolism

Background

Bacillus subtilis is attractive for industrial use for a variety of reasons, including its rapid growth rate, ability to secrete proteins into the medium, and its ‘generally regarded as safe’ (GRAS) status [1,2]. B. subtilis is also one of the best-characterized model microorganisms, as a result of extensive biochemical, genetic, and molecular biological studies [3,4]. B. subtilis has been used for the industrial production of enzymes for detergents, foods, and beverages. In industrial-scale production of enzymes, improvement of production levels is a major topic of interest.

We previously reduced the size of the B. subtilis genome by deleting unnecessary regions in order to construct a simplified microbial cell ‘factory’ for recombinant enzyme production. To do this, we constructed a multiple-deletion mutant strain, MGB874, via the sequential deletion of 865 genes (874 kb; 20.7%) from B. subtilis strain 168 [5,6]. As compared to strain 168, strain MGB874 shows enhanced production of the exogenous secreted alkaline cellulase Egl-237 [7] and alkaline protease M-protease [8] from plasmid-encoded genes in modified 2xL-Mal medium, a model medium for industrial protein production.

We have also shown that deletion of the rocR gene is an important contributor to the high level of enzyme production that we observe in genome-reduced strain MGB874 [9]. The RocR protein is a positive regulator of genes related to the arginine degradation pathway, including RocG, a major glutamate dehydrogenase [10-13]. RocG has another role as a regulatory protein that inhibits GltC, a transcription activator protein of the gltAB operon, which encodes glutamate synthase [14]. Thus, in strain MGB874, deletion of rocR not only inhibits glutamate degradation pathway but also activates the glutamate synthesis pathway (Figure  1). We proposed that this change of glutamate metabolism in strain MGB874 increases the flux from 2-oxoglutarate to glutamate, which might lead to increased syntheses of the other amino acids via transamination, finally resulting in enhanced enzyme production [9].

thumbnailFigure 1. Major reactions and regulation involved in glutamate metabolism in B. subtilis. Proteins are shown as ovals. RocG, glutamate dehydrogenase; GltAB, glutamate synthase (GOGAT); GlnA, glutamine synthetase (GS). In B. subtilis, glutamate can be degraded by RocG. B. subtilis has a glutamine synthetase-glutamate synthase (GS-GOGAT) pathway for assimilation of ammonia. The RocR and GltC transcription factors positively regulate rocG and gltAB, respectively, and GltC can be inhibited via interaction with RocG. Open and closed gray ovals indicate proteins corresponding to genes that have been deleted or inactivated, respectively, in strain MGB874. Deletion of rocR in strain MGB874 decreases expression of rocG, which leads to an increase in expression of gltAB due to activation of GltC via disinhibition by RocG.

Additionally, we found that RocG also serves as an important factor influencing enzyme production by helping to prevent acidification of the growth medium. Decreased expression of rocG reduces the level of deamination of glutamate, a major cellular ammonia-releasing reaction [15], and leads to a decrease in the external pH during strain MGB874 cultivation [16]. We found that the decreased external pH impaired production of the alkaline α-amylase AmyK38, accompanied by the induction of expression of htrA and htrB, which encode serine-type surface proteases and are known to be CssRS dependent [16]. In B. subtilis, the CssRS two-component system responds to the accumulation of misfolded proteins at the membrane-cell wall interface [17]. Alkaline α-amylase AmyK38 is thought to fold ineffectively at acidic external pH, leading to secretion stress. Therefore, at least in terms of the production of the alkaline α-amylase AmyK38, RocG appears to have a positive role in preventing acidification of the growth medium.

The aim of the present study was to enhance enzyme production in genome-reduced strain MGB874 through further optimization of glutamate metabolism. Belitsky et al. reported that rocG is still expressed at a low level due to read-through transcription of the upstream gene yweA, even in the absence of the RocR activator sequence [18]. Thus, deletion of rocG might release repression of gltAB in strain MGB874 completely, further enhancing enzyme production. However, we previously observed that deletion of rocG in strain MGB874 (strain 874ΔrocG) led to a dramatic decrease in production of the alkaline cellulase Egl-237, even in spite of an observed increase in cell yield [9]. At that time, it remained unclear if this phenomenon is caused by acidification of the growth medium, as in the case of alkaline α-amylase production. Here, we investigated the mechanisms underlying decreased enzyme production in strain 874ΔrocG and attempted to boost production of alkaline cellulase Egl-237 by overcoming the rate-limiting factors we identified.

Results and discussion

Growth characteristics of strains MGB874 and 874ΔrocG producing alkaline cellulase Egl-237

In our recent study, we found that deletion of the rocG gene in the genome-reduced strain MGB874 dramatically decreased the level of production of the alkaline cellulase Egl-237, despite an increase in cell yield [9]. Previous studies showed that mutations in rocG result in the rapid accumulation of suppressor mutations in gudB, a second, cryptic glutamate dehydrogenase gene harboring an insertion of three amino acids with respect to the common ancestral GluDH sequence [11,19,20]. However, sequence analysis of gudB alleles in strains MGB874 and 874ΔrocG revealed that the insertion mutation of the three amino acids has been retained in these strains.

To obtain insight into the mechanism responsible for decreased enzyme production in strain 874ΔrocG, we conducted time course analyses of production of alkaline cellulase Egl-237 in strains MGB874 and 874ΔrocG under batch fermentation conditions achieved using a 30-liter jar fermentor. As shown in Figure  2A and 2B, after the transition phase, production of alkaline cellulase Egl-237 in strain 874ΔrocG dramatically decreased as compared with strain MGB874, although the cell yield in strain 874ΔrocG was higher. Additionally, in the culture medium at the transition phase, we observed a decrease in pH and ammonium depletion for strain 874ΔrocG as compared to strain MGB874 during cultivation (Figure  2C and 2D).

thumbnailFigure 2. Growth characteristics of strains MGB874 and 874ΔrocG producing the alkaline cellulase Egl-237. Strains MGB874 (open circles) or MGB874∆rocG (closed circles) were transformed with pHYS237 for production of alkaline cellulase Egl-237. The strains were cultured in 2xL medium containing 7.5% (w/v) maltose monohydrate by batch fermentation with a 30-L jar fermentor. Cell yield (A), extracellular cellulase activity (B), external pH of the growth media (C) and ammonia concentration in the growth media (D) were measured at the indicated times. Arrows indicate the point at which transcriptome analyses were conducted.

Comparison of transcriptome profiles of strains MGB874 and 874ΔrocG

We then compared transcriptome profiles of MGB874 and 874ΔrocG cells at transition phase (at 18 h, indicated by arrow in Figure  2) using a custom Affymetrix tilling chips. The top-ranked 20 up-regulated genes and bottom-ranked 20 down-regulated genes in 874ΔrocG cells were listed in Tables  1 and 2, respectively. Firstly, we found that expression of htrA was markedly induced in 874ΔrocG cells (Table  1). Our previous study revealed that the decrease in external pH impaired secretion of alkaline α-amylase AmyK38 in strain MGB874, and induced htrA and htrB expression [16]. Indeed, expression of htrB was also induced in 874ΔrocG cells (4.62 fold) as compared to strain MGB874 cells in our transcriptome analysis. Additionally, time course analysis using qRT-PCR confirm that htrB expression is up-regulated in 874ΔrocG cells during early stationary phase (from 18 to 24 h, Figure  3). These results suggest that acidification of the growth medium might impair secretion of alkaline cellulase Egl-237 in 874ΔrocG cells.

thumbnailFigure 3. Time course of transcription during growth of B. subtilis strains MGB874 and 874ΔrocG. The strains MGB874 (open circles) and 874∆rocG (closed circles) were transformed with pHYS237. The transformants were cultured using shake-flask fermentation. Transcript levels for htrB, nrgA and gltA were determined by qRT-PCR (primers shown in Additional file 2: Table S1). Transcript levels were normalized to 16S rRNA levels. Error bars represent standard deviations (n=3).

Table 1. Genes up-regulated in 874ΔrocG cells (top-ranked 20 genes)

Table 2. Genes down-regulated in 874ΔrocG cells (bottom-ranked 20 genes)

Importantly, we found that many of the genes that are activated or repressed in 874ΔrocG cells are controlled by the transcriptional factor TnrA. Indeed, 10 of the bottom-ranked 20 genes and 8 of the top-ranked 20 genes were members of the TnrA regulon (Tables  1 and 2). TnrA is a major transcription factor in B. subtilis that controls gene expression under nitrogen-limited growth [23-25]. Time course analysis revealed that nrgA, an ammonia transporter gene regulated by TnrA, is transiently up-regulated in 874ΔrocG cells just before cells enter the stationary phase (at 18 h, Figure  3), which corresponds to the point that ammonium depletion occurs in the culture medium during culture of strain 874ΔrocG (Figure  2D). These results clearly indicate that nitrogen starvation is induced in 874ΔrocG cells likely due to ammonium depletion in the culture medium.

Expression of glutamate synthase (GltAB) is also known to be negatively regulated by TnrA [26], in addition to its regulation by GltC. Indeed, expression of gltA in 874ΔrocG cells significantly decreased after depletion of ammonium to levels lower than that in MGB874 cells, although gltA levels in 874ΔrocG cells were much higher than levels in MGB874 cells before entering stationary phase (at 18 h, Figure  3). These results indicate that although activation of the glutamate synthetic pathway is induced via deletion of rocG during the early growth phase as expected, it is subsequently suppressed by depletion of ammonium in the culture medium.

Cultivation using the NH3-pH auxostat approach improves enzyme production in strain 874ΔrocG

To exclude the influence of decreased pH and depletion of ammonia in the growth medium associated with culture of strain 874ΔrocG, we next performed pH-stat fermentation using NaOH or aqueous NH3 and a 2-L jar fermentor (Figure  4). The pH of the growth media was adjusted to 7.2, which corresponds to the highest pH observed in the growth medium of strain MGB874 in the absence of pH control (Figure  4A). Additionally, to prevent the carbon source from becoming a limiting factor, the initial concentration of maltose in the growth media was increased from 7.5% to 12.5%, which is sufficient in these fermentation conditions (data not shown).

thumbnailFigure 4. Growth characteristics of strains MGB874 and 874ΔrocG producing alkaline cellulase Egl-237. The strains MGB874 (open symbols and dotted lines) and 874∆rocG (closed symbols and solid lines) were transformed with pHYS237, and cultured in 2xL medium containing 12.5% (w/v) maltose monohydrate by the pH-Stat fermentation using 2-L jar fermentor. Fermentation without pH control was done as a reference (A). The pH was adjusted to 7.2 by the automatic addition of 1M NaOH (B) or 10% (w/v) aqueous NH3 (C). Cell yields (circles) and extracellular cellulase activities (triangles) were shown on the left side of the figure. Residual ammonia concentrations (diamonds) and external pHs (crosses) in the growth media were shown on the right side of the figure. Additionally, total amounts of ammonia fed (squares) were also displayed under the NH3-pH auxostat. Arrows indicate the point at which transcriptional analysis was conducted.

When fermentation was performed without pH control, the growth characteristics were similar to the results shown in Figure  2. On the other hand, when pH-stat fermentation using NaOH was performed, the production of alkaline cellulase Egl-237 in strain 874ΔrocG was improved to nearly the same level as that observed for strain MGB874 (Figure  4B). In both these cases, the concentrations of ammonia were significantly decreased as compared to those reached during cultivation without pH control. To examine if the decrease in ammonia affects production of alkaline cellulase Egl-237, we performed pH-stat fermentation using aqueous NH3, using a so-called NH3-pH auxostat [27] (Figure  4C). The enzyme production period in strain 874ΔrocG was prolonged with use of the NH3-pH auxostat, whereas the production profile of alkaline cellulase Egl-237 in MGB874 cells was similar in both cultivation conditions. With the NH3-pH auxostat, the production of alkaline cellulase Egl-237 in strain 874ΔrocG was 1.67-fold higher than that in strain MGB874 at the end of the cultivation period (Figure  4C). Production of alkaline cellulase Egl-237 in strain 874ΔrocG corresponded to about 5.5 g l-1, the highest level reported so far [6].

Notably, the level of residual ammonia in the growth medium from strain 874ΔrocG was lower than that from strain MGB874, although the total amount of ammonia introduced into the growth medium for strain 874ΔrocG was considerably larger than that for strain MGB874 (Figure  4C). These data suggest that the ratio of assimilated ammonia in 874ΔrocG cells was higher than that in MGB874 cells and furthermore, that assimilation activity is maintained through late stages of cultivation.

It should be noted that the rocG deletion in wild-type strain 168 (168ΔrocG) also enhanced production of alkaline cellulase Egl-237 with the NH3-pH auxostat (Additional file 1: figure S1). In this experiment, we also confirmed that the insertion mutation of the three amino acids was retained in strain 168ΔrocG. Notably, the production level from strain 168ΔrocG (2.8 g l-1) was about half of that of strain 874ΔrocG, indicating the importance of the genetic background of the reduced-genome strain for higher levels of alkaline cellulase Egl-237 production.

Additional file 1: Figure S1. Cell yield and alkaline cellulase Egl-237 production under the NH3-pH auxostat, The alkaline cellulase Egl-237 overproducing strains in the presence (+) or absence (−) of rocG were cultured by the pH-Stat fermentation. The pH was adjusted to 7.2 by addition aqueous NH3. The cell yields (at 42 h; open circles) and the cellulase activities in growth media (72h; black bars) were measured. (A) The wild-type strain 168 and strain 168∆rocG. (B) The genome-reduced strain MGB874 and strain 874∆rocG.

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Changes in gene expression underlying improvement in enzyme production with pH-stat fermentation

To investigate the changes in gene expression underlying the improvement of enzyme production in 874ΔrocG cells under pH-stat fermentation, RNA was extracted from cells at 24 h of cultivation (Figure  4; arrows), and expression levels of selected genes were measured by qRT-PCR (Figure  5). Although transcriptional levels for selected genes were not significantly changed in MGB874 cells under any fermentation conditions, remarkable changes in expression of these genes were observed in 874ΔrocG.

thumbnailFigure 5. Transcriptional levels of selected genes in strains MGB874 and 874ΔrocG. The strains MGB874 (A) and 874∆rocG (B) were transformed with pHYS237, and cultured by the pH-Stat fermentation. Fermentation without pH control was done as a reference (a). The pH was adjusted to 7.2 by addition of NaOH (b) or aqueous NH3 (c). RNA was isolated from the cells at the 24 h of the cultivation time (indicated by arrows in Figure 4), and expression level of htrB, nrgA, gltA and citB were determined by qRT-PCR. The transcriptional levels are expressed relative to those of 16S rRNA. Error bars represent standard deviations (n=3).

Firstly, expression of htrB was reduced to the same level in strain MGB874 under fermentation conditions with pH-control not only with aqueous NH3 but also with NaOH, clearly indicating that the CssRS-dependent secretion stress response is induced by overproduction of alkaline cellulase Egl-237 in 874ΔrocG cells under the low external pH condition (Figure  5). Notably, production of alkaline cellulase Egl-237 did not induce the secretion stress response in MGB874 cells (Figures  3 and 5) but overproduction of alkaline α-amylase AmyK38 induced this response to a high degree in MGB874 cells [16]. Because the decrease of external pH was more severe in 874ΔrocG cultivation (without pH control) compared to that in MGB874 cultivation (Figure  4A), the threshold value of external pH leading to secretion stress responses for overproduction of alkaline cellulase Egl-237 would be lower than for the overproduction of AmyK38.

We also found that expression of nrgA, known to be activated under nitrogen-limited growth, was down-regulated in 874ΔrocG cells using the NH3-pH auxostat, suggesting avoidance of nitrogen starvation (Figure  5). Furthermore, the expression level of gltA, encoding a subunit of glutamate synthase, was 9-fold higher in 874ΔrocG cells than in MGB874 when using the NH3-pH auxostat (Figure  5). As ammonia can be assimilated via the glutamine synthetase-glutamate synthase (GS-GOGAT) pathway in B. subtilis (Figure  1), activation of the glutamate synthetic pathway might indirectly contribute to the enhancement of ammonia assimilation ability in 874ΔrocG cells (Figure  4C and 5). With the NH3-pH auxostat, the continuous conversion of ammonia to glutamate in 874ΔrocG cells might lead to increased flux in the synthesis of other amino acids via transamination, resulting in enhanced production of alkaline cellulase Egl-237.

As mentioned, enzyme productivity lasted through the end of the cultivation period in strain 874ΔrocG with use of the NH3-pH auxostat but this was not observed for strain MGB874 under the same conditions (Figure  4C). Activation of the glutamate synthetic pathway in 874ΔrocG cells could account for this difference. Furthermore, we found that expression of the gene encoding aconitase (citB) was up-regulated in 874ΔrocG cells but not MGB874 cells under NH3-pH auxostat (Figure  5). Expression of citB has been reported to be indirectly repressed by 2-oxoglutarate, which competitively represses the reaction of citrate synthase (CitZ), leading to repression of citB by the transcriptional regulator CcpC in the absence of the effector citrate [28,29]. Therefore, improvement of metabolic flux from 2-oxoglutarate to glutamate in strain 874ΔrocG might lead to activation of citB due to inactivation of the repressor CcpC. Blencke et al. reported that TnrA exerts a weak activating effect on citB expression [30]. However, in our experiment, the expression levels of TnrA regulated gene nrgA were almost the same in strains MGB874 and 874ΔrocG under NH3-pH auxostat (Figure  5). Thus, it seems that TnrA did not participate in activation of citB in strain 874ΔrocG, compared to that of strain MGB874 under NH3-pH auxostat. Activation of citB might contribute to prolonged high enzyme productivity through the generation of reducing power via the tricarboxylic acid (TCA) cycle.

Conclusion

Here, we describe conditions resulting in the highest levels of production of alkaline cellulase Egl-237 in B. subtilis cells reported to date. We found that deletion of the glutamate dehydrogenase gene rocG in the genome-reduced strain MGB874 (874ΔrocG) and cultivation of 874ΔrocG using NH3-pH auxostat conditions leads to enhanced enzyme production through prolonged high enzyme productivity until the end of cultivation. This beneficial effect is very likely a consequence of an enhanced metabolic flux from 2-oxoglutarate to glutamate and generation of metabolic energy through activation of the TCA cycle.

Additionally, we found that the overproduction of alkaline cellulase Egl-237 causes the induction of CssRS-dependent secretion stress responses in the acidified growth medium below the threshold pH value, which is lower than that for the overproduction of alkaline α-amylase AmyK38.

With the NH3-pH auxostat, levels of alkaline cellulase Egl-237 produced by strain 874ΔrocG far exceeded those produced by the wild-type genetic-background strain 168ΔrocG, and reached the highest level reported so far, corresponding to 5.5 g/L. However, it is not clear at the moment if these improvements are attributable to a global synergistic effect of large-scale genome reduction or to individual effects of one or more specific gene deletions. To further improve enzyme production, we are presently attempting to elucidate the mechanisms underlying the improvement in productivity we have observed.

Materials and methods

Bacterial strains, plasmids, and growth media

The bacterial strains and plasmids used in this study are listed in Table  3. E. coli HB101 (Takara Bio Inc.) was used as the host for plasmid preparation and was grown in Luria-Bertani (LB) medium [1% (w/v) Bacto tryptone (Difco), 0.5% (w/v) Bacto yeast extract (Difco), and 1% (w/v) NaCl]. Strain 168ΔrocG, a rocG mutant strain derived from strain 168, was constructed in a similar way to construction of strain 874ΔrocG, which was described previously [9]. B. subtilis mutant strains were transformed with the plasmid pHYS237 for production of alkaline cellulase Egl-237, which originated from Bacillus sp. strain KSM-S237 [9], using the protoplast transformation method [31]. For enzyme production, we used 2xL medium [2% (w/v) Bacto tryptone, 1% (w/v) Bacto yeast extract, 1% (w/v) NaCl, 7.5 μg ml-1 manganese sulfate 4–5 hydrate, and 15 μg ml-1 Tet] supplemented with 7.5% (w/v) or 12.5% (w/v) maltose monohydrate.

Table 3. Bacterial strains and plasmids used in or constructed for this study

Culture methods for the assessment of alkaline cellulase Egl-237 production

For shake-flask fermentation, transformants were pre-cultured in LB medium with 15 μg ml-1 Tet with shaking at 120 rpm at 30°C for 15 h, and 600 μl of the pre-culture was inoculated into 30 ml of 2×L medium with 7.5% (w/v) maltose monohydrate in a 500-ml Sakaguchi flask.

For jar fermentation, B. subtilis harboring pHYS237 stored in 10% glycerol at −80°C were inoculated onto LB agar medium with 15 μg ml-1 Tet. After incubation at 37°C for 12 h, cells were collected and inoculated into pre-culture medium at an optical density at 600 nm (OD600) of 0.02. For batch fermentation, cells were pre-cultured in 200 ml of 2×L medium with 7.5% (w/v) maltose monohydrate with shaking at 210 rpm at 30°C to an OD600 of 0.3 to 0.5, then inoculated into a 30-L jar fermentor (working volume, 18 liters). The 30-L jar fermentor was operated at an aeration rate of 0.4 vvm and an agitation rate of 300 rpm. For pH-stat fermentation, cells were pre-cultured in 30 ml of 2×L medium with 12.5% (w/v) maltose monohydrate with shaking at 120 rpm at 30°C to an OD600 of 0.3 to 0.5, then inoculated into a 2-L jar fermentor (working volume, 0.8 liters). The 2-L jar fermentor was operated at an aeration rate of 0.5 vvm and an agitation rate of 800 rpm. The pH was kept at 7.2 via automatic addition of 1M NaOH or 10% (w/v) aqueous NH3. Fermentation without pH adjustments was used as a control. As appropriate to specific assays, cultured cells were removed by centrifugation at 9,000 × g and the supernatants were stored at −30°C. For RNA extraction, cells were separated by centrifugation, washed with 10 mM Tris–HCl (pH 7.5), frozen with liquid nitrogen, and stored at −80°C.

Analytical methods and cellulase activity

The concentration of ammonia and maltose in the culture supernatants was determined by enzymatic analysis according to the F-Kit UV method (Boehringer GmbH). Cellulase activity in the culture medium was determined as described previously [9]. The amount of enzyme required for release of 1 μmol of p-nitrophenol per minute was defined as 1 U.

High-resolution transcriptome analysis

Total RNA was extracted from B. subtilis cells as described previously [32]. Synthesis of cDNA, terminal labeling, and oligonucleotide chip hybridization were performed as described in the Affymetrix instruction manual. Transcriptional signals were analyzed and visualized along genome coordinates using the program IMC Array Edition (In Silico Biology, Japan). The signal intensities of each experiment were adjusted to confer a signal average of 500 and normalized by MA plot analysis for comparison of strains MGB874 and 874ΔrocG. [33,34]. The average signal intensities of probes in each coding sequence were calculated after removal of the lowest and highest intensities.

Quantitative real-time PCR

Quantitative real-time PCR (qRT-PCR) amplification, detection, and analysis were performed with the Mx3005P Real-time PCR system (Stratagene) and Brilliant II Fast SYBR Green QPCR Master Mix (Stratagene), as previously described [9]. The sequences of the primers used in real-time PCR were developed with Primer 3 (version 0.4.0) [35] and are listed in Additional file 2: Table S1 in the supplemental material. Experimental RNA levels were normalized to 16S rRNA levels, as previously described [16].

Additional file 2: Table S1. Oligonucleotide primers used for real-time PCR analysis.

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Abbreviations

GRAS: generally regarded as safe; CssRS: Control secretion stress Regulator and Sensor; qRT-PCR: quantitative real-time PCR; NaCl: sodium chloride; Tet: tetracycline.

Competing interests

The content of this manuscript is relevant to a patent application made by Kao Corporation (Patent no. JP2007-330255A); however, all authors declare that they have no competing interests.

Authors’ contributions

NO, KO, and KA initiated and coordinated the project. KM and YK drafted the manuscript, constructed mutant strains, evaluated production levels of alkaline cellulase Egl-237, and measured pH and ammonium concentrations in the growth medium. KM and TM performed tilling array and qPCR. ES supported our results by metabolic analysis. HT and SK processed tilling array data. NO and KO supervised the study and reviewed results. All authors have read and approved the final manuscript.

Acknowledgements

We thank Junichi Sekiguchi (Shinshu University), Kouji Nakamura (University of Tsukuba), Shu Ishikawa (Nara Institute of Science and Technology), Fujio Kawamura (University of Rikkyo), and Yasutaro Fujita (Fukuyama University) for valuable discussions. We also thank Yoshiharu Kimura and Yoshinori Takema (Kao Corp.) for valuable advice. This study was performed in collaboration with Shengao Liu (Kao Corp.), Takeko Kodama (Kao Corp.), Hiroshi Kakeshita (Kao Corp.), Tadahiro Ozawa (Kao Corp.), Hiroshi Kodama (Kao Corp.), Kazuhiro Saito (Kao Corp.), Akihito Kawahara (Kao Corp.) and Nozomu Shibata (Kao Corp.). This research was conducted as part of the Project for the Development of a Technological Infrastructure for Industrial Bioprocesses through R&D on New Industrial Science and Technology Frontiers of the Ministry of Economy, Trade, and Industry (METI), Japan, and was supported by the New Energy and Industrial Technology Development Organization (NEDO), Japan.

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