INTRODUCTION

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Xylan is a major component of hemicellulose in plant cell walls. It is covalently and noncovalently attached to cellulose, lignin, pectin, and other polysaccharides to maintain cell wall integrity (18). Enzymes that degrade xylan have many useful industrial applications, including the conversion of lignocellulosic material to fuels and chemicals (9) and the processing of hemicellulose to paper (5, 12, 39). During the process of pulp bleaching, for example, xylanases have been used instead of chlorine to increase the extractability of lignin for the production of high-quality paper (10). The use of xylanase to either replace or reduce the amount of chlorine used in pulp bleaching would have a strong positive effect on the environmental impact of the process. The widespread use of xylanase for pulp bleaching, however, has been limited by the high temperature and alkaline pH of pulp-bleaching processes, since most available xylanases are not active under these conditions. Furthermore, the use of xylanase for commercial pulp bleaching requires low-cost, high-volume production of the enzyme.

Streptomyces species are gram-positive soil bacteria that produce and export a variety of hydrolytic enzymes that enable them to utilize complex carbohydrates in their natural habitats. Compounds such as xylan, chitin, and starch, as well as cellulosic plant material, serve as the primary sources of carbon, nitrogen, and energy for these organisms. The genes for several of the enzymes involved in complex-carbohydrate utilization have been cloned and partially characterized, although relatively little is known about their regulation. Perhaps the best-studied examples, from the point of view of gene regulation, are the -amylase, chitinase, and agarose genes.

The agarase gene, dagA, has four promoters (6) and is transcribed by at least three different RNA polymerase holoenzymes (7). At least one of the promoters has been shown to respond to carbon source regulation. Regulation of -amylase, somewhat surprisingly, varies from species to species and is dependent on the streptomycete host used for study. Expression of the Streptomyces griseus (38) and S. venezuelae (41) genes is induced by maltose and repressed by glucose in their native hosts. The -amylase of S. thermoviolaceus (1) is induced by maltotriose and repressed by mannitol but not glucose in S. thermoviolaceus. The S. limosus -amylase gene is induced by maltose in S. limosus, S. lividans, and S. coelicolor but the pattern of repression is different in the three species (40). In S. limosus, expression is repressed by mannitol but not glucose. In S. lividans and S. coelicolor, expression is repressed by glucose but not mannitol.

Chitinase genes have been cloned from S. olivaceoviridis (3), S. thermoviolaceus (35), S. plicatus (28, 29), S. griseus (25), and S. lividans (13). Delic et al. (11) examined the regulation of the S. plicatus chi63 gene in S. lividans and showed that expression of chi63 is induced by partially hydrolyzed chitin and repressed by glucose at the level of transcription initiation. A series of cis-acting mutations within the chi63 promoter region identified bases important for regulation as well as RNA polymerase recognition (24). An operator consisting of a perfect 12-bp direct-repeat sequence was identified and shown to be the site of both glucose repression and chitin induction (24). Work describing promoter mutations, taken together with work on mutations that affect repressor proteins (11, 16, 24, 36), provides evidence that glucose repression of some catabolite-controlled genes in Streptomyces may act through the same repressor proteins and operator sequences that are involved in substrate induction.

Here we report the cloning and partial characterization of a xylanase gene from S. coelicolor that is 99% identical to the xylanase B gene of S. lividans (20, 32) and the use of the expression and localization signals of this gene to express and secrete a thermostable xylanase from Thermotoga maritima. The S. lividans xylanase B gene encodes a protein of 31 kDa and has been characterized biochemically (20). By using enzyme activity assays, xylanase expression was detected in S. lividans cells grown on xylan as the sole carbon source but not in cells grown on xylan plus glucose (2). From an analysis of the DNA sequence of the cloned S. lividans xlnB gene, a putative translation start site and signal sequence-processing site was suggested (26, 33) based on homology to other xylanase genes and signal sequences (42). To investigate the regulation of the S. coelicolor xylanase B gene, we constructed a transcriptional fusion between the promoter region and the xylE reporter gene and examined expression on various carbon sources in S. lividans. Expression of the xlnB-xylE fusion was induced by xylan and repressed by glucose, and we conclude that regulation by glucose and xylan is at the level of transcription initiation. Using both primer extension analysis and in vitro transcription assays, we identified an apparent transcription start site for xlnB that is downstream of the translation start site previously predicted (26, 33). Deletion analysis of the promoter region identified sequences between 268 and 318 to be involved in glucose repression. By using the promoter and signal sequence of the xlnB gene, an in-frame fusion was made to the coding region of the T. maritima xynA gene (8). Expression of the recombinant protein was readily detected in Streptomyces, and the activity of the enzyme was thermostable and localized extracellularly.

	MATERIALS AND METHODS

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Construction and screening an S. coelicolor genomic library. Chromosomal DNA was isolated from S. coelicolor A(3)2 as described previously (17) and partially digested with Sau3A. DNA fragments between 2 and 7 kb in size were selected by agarose gel electrophoresis and isolated with the Geneclean II Kit (Bio 101, Inc.). A library of these fragments was constructed by ligation to BamHI-digested pUC19 with T4 DNA ligase (Boehringer). Recombinant plasmids were introduced into Escherichia coli JM83, plated on Luria-Bertani agar plates containing 1.5 mg of 4-O-methyl-D-glucurono-D-xylan-Remazol Brilliant Blue R (Sigma) per ml and 50 µg of ampicillin (Sigma) per ml, and incubated at 37°C for 16 h. Colonies were inspected for clear zones indicating xylan hydrolysis.

Subcloning and sequencing. Two plasmid-containing clones showing xylan hydrolysis, one of which, pCC76, is shown in Fig. 1, were analyzed by restriction digestion and the chromosomal fragment within them was subcloned into M13mp18 and M13mp19 for DNA sequencing. The nucleotide sequence was determined by the method of Sanger et al. (31) with the pUC forward and reverse primers as well as primers synthesized at the University of Georgia Molecular Genetics Instrumentation Facility, Athens. Primers were end labeled with [-³²P]ATP (Amersham) by using polynucleotide kinase (Promega). Reactions were performed by using the fmol sequencing system (Promega) in a thermocycler (Ericomp Inc.). DNA sequences were analyzed with University of Wisconsin Genetics Computer Group software.

View larger version (7K): [in this window] [in a new window]   FIG. 1.   Restriction maps of the fragment cloned from S. coelicolor, resulting in xylanase activity.

Construction of a xlnB promoter-xylE fusion. A DNA fragment containing the xlnB promoter was amplified from pCC76 by PCR. The primers contained additional sequence to include restriction endonuclease cleavage sites for directional cloning into plasmid pXE4 (19), which contains a promoterless copy of the xylE gene. Oligonucleotide 5'-aactgcagCCCGCGCGTTGCCCTGTGA-3', which was synthesized to include a PstI recognition sequence at the 5' end (PRIMER 1 in Fig. 2), was the upstream primer, and oligonucleotide 5'-cgcggatccGTCGGCCTGGGCGGTGCCCG-3', which was synthesized to include a BamHI recognition sequence at the 3' end (PRIMER 3 in Fig. 2), was the downstream primer. PCRs were carried out with Taq DNA polymerase (Boehringer) and a thermocycler (Ericomp Inc.). PCR products were digested with PstI-BamHI, ligated into PstI-BamHI-digested pUC19, removed as a HindIII-BamHI fragment, and ligated into HindIII-BamHI-digested pXE4. Plasmid DNA isolated from E. coli DH5MCR (Bethesda Research Laboratories) was used for subsequent transformation into S. lividans 1326. The DNA sequence of the cloned fragment was determined as described above.

View larger version (24K): [in this window] [in a new window]   FIG. 2.   DNA sequence and predicted protein sequence of the 5' end of the S. lividans xlnB gene. Bars indicate the DNA sequence included in oligonucleotide primers used in the PCRs and primer extension analysis described in the text. The first ATG in boldface type indicates the previously predicted translation start site (26, 32), and the amino acid sequence in boldface type indicates the previously predicted peptide signal sequence (26, 32). The G in the DNA sequence indicated in boldface type is the base identified in our analysis as the transcription start site. The second ATG in boldface type indicates a potential translation start site downstream of this apparent transcription start site.

Catechol dioxygenase assays. Spores of S. lividans containing pCC88 (Table 1) were germinated for 28 h in NMMP minimal medium (17) containing 0.5% glycerol. Mycelia were collected and washed twice with NMMP and then grown in NMMP containing the indicated carbon source. To examine xlnB expression in the presence of different carbon sources, pregerminated mycelia of S. lividans containing various promoter-xylE fusions were grown for 18 h in NMMP medium containing the carbon source indicated at 0.5%. Cells were sampled, harvested, and washed with 20 mM potassium phosphate buffer (pH 7.2). Catechol dioxygenase activity was assayed as described previously (19) with some modifications. The cells were lysed by sonication for 1 min in 10 µl of Triton X-100 per ml and incubated on ice for 15 min. Lysates were centrifuged at 4°C for 20 min, and supernatants were assayed for catechol dioxygenase activity. The protein concentration was measured by the method of Bradford (4) with a protein assay kit (Bio-Rad Laboratories, Inc.). For catechol dioxygenase assays, 0.5 mg of protein was suspended in a final volume of 500 µl of 100 mM phosphate buffer (pH 7.5) and then mixed with 500 µl of prewarmed (37°C) 0.4 mM catechol. The activity of dioxygenase is expressed as the rate of change in the optical density at 373 nm per minute per milligram of protein.

Primer extension analysis. Spores of S. lividans 1326 containing pCC88 were grown at 30°C for 48 h in liquid NMMP medium (17) containing 0.5% oatspelt xylan, with shaking at 245 rpm. Total cellular RNA was isolated (27) and used for primer extension reactions as previously described (11). An oligonucleotide, 5'-CCACCCTTCGCCGCGCCGTAAGGCAC-3', complementary to the 5' end of the fragment containing the xylE gene (24) was used to prime the reaction. A DNA sequencing ladder was generated with the same primer, using pCC88 as template.

Preparation of RNA polymerase. S. lividans 1326 cells were grown in YEME medium (17) at 30°C for 46 h. Mycelia were harvested (30 g [wet weight]), washed twice with buffer A (34), and disrupted by two passages through a French pressure cell at 16,000 lb/in². The lysed cells were centrifuged at 15,000 × g for 60 min at 4°C, and the supernatant was passed through a heparin-agarose column (Sigma) equilibrated with buffer A containing 50 mM KCl. The column was eluted in one step with buffer A containing 750 mM KCl. Fractions (1 ml) containing the peak protein concentration were used in in vitro transcription assays.

In vitro transcription assays. To prepare templates for in vitro transcription, two DNA fragments (see Fig. 7A) were amplified by PCR with pCC88 as the template. The oligonucleotide 5'-aactgcagCCCGCGCGTTGCCCTGTGA-3' (PRIMER 1 in Fig. 2), was the 5' primer for both reactions. Two different oligonucleotides, 5'-cgcggatccGTCGGCCTGGGCGGTGCCCG-3' (PRIMER 3 in Fig. 2), and 5'-CTGCGACGCCTCGGCTGGACG-3' (PRIMER 2 in Fig. 2), were used for 3' priming. In vitro transcription assays were performed as previously described (15). ³²P-labeled RNA was displayed on a 9% acrylamide-7 M urea gel. MspI-digested pBR322 was incubated with [-³²P]dCTP and Klenow fragment to prepare molecular weight markers.

Construction of an XlnB-XynA protein fusion. Plasmids used in this portion of the study are listed in Table 1. The xynA open reading frame (ORF) was amplified from pCC16 template DNA with PCR primers 5'-cgcggatccATGCAAGTCAGGAAGAGAC-3' (TM PRIMER 1 in Fig. 3) as the upstream primer and 5'-cgcggatccCTCACTTGATGAGCCTGAG-3' (TM PRIMER 2 in Fig. 3) as the downstream primer; these primers were synthesized to include a BamHI site at either end. The xlnB promoter and signal sequence were amplified with PRIMER 1 and PRIMER 3 (see Fig. 2). Diagrams of the construction of high-copy-number (Fig. 4A) and low-copy-number (Fig. 4B) expression vectors are shown. Ligation of the fragments to generate an in-frame fusion between the end of the xlnB signal sequence and the ATG of the xynA gene was confirmed by DNA sequence analysis of the final construction.

View larger version (36K): [in this window] [in a new window]   FIG. 3.   Partial nucleotide sequence of the T. maritima xynA gene and predicted amino acid sequence of the gene product. The putative leader peptide is shown in boldface type (44). Bars above the DNA sequence indicate primers used in PCRs.

View larger version (27K): [in this window] [in a new window]   FIG. 4.   Construction of pCC20 (A) and pCC26 and pCC27 (B).

Oligonucleotide-directed mutagenesis of the xynA gene. Two leucine residues encoded by TTA in the xynA gene were changed to CTA by oligonucleotide-directed mutagenesis as described previously (21, 22). Two oligonucleotides, 5'-GAAAACCCGCTAgAATCCCACC-3' (MUT PRIMER in Fig. 3) and 5'-ACGGTACTAgGATCTCTTTCCAGTG-3' (MUT PRIMER in Fig. 3) were used as mutagenesis primers. (The lowercase letters indicate the base change introduced.) Single-stranded pCC18mp19 (Table 1) containing the xynA coding sequence, was used as the template. E. coli DH5F' was used for propagation of plasmids and M13 phage, and E. coli BW313 was used to prepare uracil-substituted single-stranded DNA for mutagenesis (30). Plasmid pCC21mp19 (Table 1) containing the mutagenized xynA ORF was analyzed by DNA sequencing.

Xylanase assays. Spores of S. lividans or S. lividans containing various plasmid constructions were grown for the times indicated in NMMP minimal medium (17) containing 0.5% oatspelt xylan, and the cells were harvested by centrifugation. Mycelia were lysed with a sonicator to prepare cell extracts. Protein in the culture supernatant (10 ml) was precipitated with 3 volumes of cold ethanol, suspended in 1 ml of 0.1 M sodium acetate (pH 5.5), and dialyzed against 0.1 M sodium acetate (pH 5.5) in 25,000-molecular-weight-cutoff-dialysis tubing (Spectra). The protein concentration was determined by the method of Bradford (4). Xylanase activity was determined as described previously (8). To test thermostable activity, samples were preheated at 85°C for 15 min and incubated with 1% birchwood xylan in 0.1 M sodium acetate (pH 5.5) at 90°C for 10 min. One unit of xylanase activity is defined as the amount of enzyme required to liberate 1 µmol of reducing equivalent (as xylose equivalents) per min.

	RESULTS

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Cloning the xylanase B gene from S. coelicolor. A chromosomal library of S. coelicolor DNA was constructed in E. coli JM83 by using pUC19 and screened for clones expressing xylanase activity on Luria-Bertani agar plates containing 4-O-methyl-D-glucurono-D-xylan-Remazol Brilliant Blue R. Xylanase activity was assayed by visual inspection of plates after incubation at 37°C for 16 h. Positive clones, detected by the presence of clear zones around colonies suggesting xylan hydrolysis, were recovered at a frequency of approximately 1 in 5,000 colonies. pCC76, shown in Fig. 1, contained a 3.3-kb DNA fragment with an ORF that was 99% identical to the xylanase B gene of S. lividans. We therefore designate this gene from S. coelicolor xlnB. Also contained on this fragment was an ORF identical to an acetylxylan esterase, axeA, from S. lividans (32), an extended region upstream of xlnB, and an ORF that is identical to the RNase P gene from S. lividans (32).

Detection of xlnB promoter activity by using a transcriptional fusion to the xylE reporter gene. Using the information previously reported for the xlnB gene of S. lividans (26, 33), PCR was used to amplify a DNA fragment containing the sequences from 375 to +126 with respect to the putative translation start site (first bold ATG) shown in Fig. 2. This fragment was cloned upstream of a promoterless copy of a catechol dioxygenase (xylE) reporter gene (19), and this fusion, contained on plasmid pCC88, was used to assay xlnB expression. S. lividans cells containing pCC88 were grown in medium containing either oatspelt xylan or birchwood xylan. Expression from the xlnB promoter was induced by both oatspelt and birchwood xylans, but oatspelt xylan was the more efficient of the two (Fig. 5). Oatspelt xylan was used as the inducer in all subsequent experiments to examine xlnB promoter expression.

View larger version (20K): [in this window] [in a new window]   FIG. 5.   Induction of the xlnB-xylE transcriptional fusion. Pregerminated spores of S. lividans containing pCC88 were grown in NMMP containing either oatspelt xylan or birchwood xylan as the sole carbon source. Enzyme activity is defined in milliunits per milligram and is calculated as the rate of change in the optical density at 373 nm per minute per milligram of protein.

Transcription from the xlnB promoter is strongly repressed by glucose and cellobiose. To examine the regulation of xlnB expression, cells containing the xlnB-xylE fusion were grown on a variety of carbon sources (Table 2). While expression of the xlnB-xylE fusion was most strongly induced by xylan, expression was also detected during growth on arabinose to a level of almost 50% of that on xylan. While some simple sugars such as mannitol, galactose, and xylose partially repressed induction by xylan, the most dramatic repression was with either glucose or cellobiose in the growth medium. These data extend the analysis of Bertrand et al. (2), who showed that xylanase activity was detected in cells grown on xylan but not xylan plus glucose, and indicate that regulation of xylanase expression by simple sugars is at the level of transcription initiation.

Identification of an apparent transcription start site for the xlnB promoter by primer extension analysis. S. lividans cells containing the xlnB gene on plasmid pCC88 were grown in minimal liquid medium (17) containing 0.5% oatspelt xylan with or without glucose, and RNA was isolated as previously described (17). An oligonucleotide complementary to the beginning of the fragment containing the xylE gene (24) was used to initiate reverse transcription of xlnB-generated RNA. As shown in Fig. 6, a primer extension product was generated in reaction mixtures containing RNA from both xylan and xylan plus glucose but the amount of product generated from xylan-plus-glucose-grown cells was much smaller than that detected from xylan-grown cells. These results support the observations from analysis of the xlnB-xylE fusion, indicating that expression of xlnB is repressed by glucose and that regulation is at the level of transcription initiation.

View larger version (75K): [in this window] [in a new window]   FIG. 6.   Primer extension analysis of RNA isolated from S. lividans cells grown on either xylan (lane 1) or xylan plus glucose (lane 2) as the carbon source. The sequence ladder to the left is the DNA region around the inferred transcription start site of xlnB.

Identification of an apparent transcription start site in in vitro transcription assays. Given the results obtained by primer extensions analysis, a second method was used to determine the transcription start site. Two DNA fragments were prepared by PCR amplification for use as templates in in vitro transcription assays. One contained the apparent transcription start site identified by primer extension and would generate a runoff transcript of 79 bases from this start site. The other had this site deleted and would not generate a run off transcript from the putative promoter identified by primer extension analysis. The deleted fragment would, however, probably contain a promoter upstream of the putative translation start site predicted from sequence analysis (32, 37), if one existed. RNA polymerase was prepared from S. lividans, and in vitro transcription assays were performed as previously described (43). As shown in Fig. 7, a run off transcript of the size predicted from the primer extension analysis was readily detected in reaction mixtures containing the DNA fragment with the intact promoter region. No transcript of the size predicted from signal sequence analysis was detected in reaction mixtures containing the DNA fragment with the apparent start site deleted, and there was no evidence of a promoter upstream of this site within the fragment. These data, taken together with the results obtained by primer extension analysis, indicate that the transcription start site of the xlnB promoter is, in fact, downstream of the translation start site previously predicted.

View larger version (30K): [in this window] [in a new window]   FIG. 7.   In vitro transcription assays of the xlnB promoter. (A) The apparent transcription start site inferred from primer extension analysis is indicated as +1. The size of the predicted transcript (79 bases) from the intact xlnB-containing fragment (top) and the size of the fragment with the predicted start site deleted (bottom) are shown. (B) Lanes 1 and 5 contain molecular weight markers, and the sizes (in thousands) are indicated by the numbers to the right. Products generated in runoff transcription reactions involving the intact promoter-containing fragment (lane 2), the fragment with the apparent transcription start site deleted (lane 3), or no DNA as template (lane 4) were separated by polyacrylamide gel electrophoresis and visualized by autoradiography.

Deletion analysis of xlnB promoter identifies sequences important for regulation and expression. To identify sequences important for the regulation of xlnB, a series of 5' promoter deletions was constructed and analyzed by using transcriptional fusions to the xylE reporter gene. As shown in Fig. 8, plasmid pCC88 contains the intact xlnB promoter region with sequences from 430 to +79 relative to the transcription start site identified in our analysis; pCC114 contains the region from 318 to +79; pCC113 contains the region from 268 to +79; and pCC112 contains the region from 216 to +79. Deletion of sequences to 318 reduced the level of expression on xylan slightly but had no effect of regulation. A deletion to 268, however, resulted in glucose-resistant expression from xlnB, suggesting that sequences between 318 and 268 relative to this apparent transcription start site contain a site required for glucose repression. A deletion to 216 severely reduced xylE expression driven by the xlnB promoter, suggesting that sequences between 268 and 216 are required for promoter activity.

View larger version (24K): [in this window] [in a new window]   FIG. 8.   Analysis of deletions of the xlnB promoter. (A) Fragments containing the intact xlnB promoter and various deletions are shown. The numbers to the left of each fragment indicate the end point of the 5' deletion. The plasmids containing these fragments are indicated on the right. (B) Histogram showing the results of quantitative catechol dioxygenase assays, plotted as percentages of the fully induced full-length promoter fusion. Cells containing each of the plasmids shown in panel A were examined after growth on glucose, xylan, or xylan plus glucose as the carbon source.

The xlnB-xynA fusion protein is expressed in S. lividans and localized extracellularly. To test expression of the xlnB-xynA fusion protein, wild-type S. lividans and cells containing various xlnB-xynA fusion plasmids were grown in NMMP minimal medium containing 0.5% oatspelt xylan and the xylanase activity in crude cell extracts and culture supernatants was tested. As shown in Table 3, by using xylanase assays performed at 50°C, activity (49.61 U/mg) was detected from wild-type S. lividans cells. This strain is known to contain several xylanases that are active at this temperature. When the assays were performed at 90°C, however, no activity was detected from wild-type S. lividans cells, suggesting that the activity detected in these cells at 50°C was not stable at 90°C. Thermostable xylanase activity was detected in cells containing each of the xlnB-xynA fusion plasmids. Plasmid pCC20 contains the intact xlnB promoter (430 to +79) driving the expression of the fusion protein on a high-copy-number plasmid, and thermostable activity was clearly detected, although at a low level (0.44 U/mg).

	DISCUSSION

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We report the cloning of a xylanase gene from S. coelicolor that is 99% identical to the xlnB gene from S. lividans and partial characterization of its regulation. To identify the promoter of xlnB, we constructed a transcriptional fusion between the 5' region of the xlnB gene and the xylE reporter gene (19) and defined a region of the gene that mediates transcription initiation and regulation. Analysis of this fusion suggests that expression of xlnB is efficiently induced by either oatspelt or birchwood xylan, although oatspelt xylan is apparently better, and that this induction is repressed by glucose or cellobiose. Furthermore, this analysis with a transcriptional fusion suggests that regulation by carbon source availability occurs, at least in part, at the level of transcription initiation. Interestingly, arabinose, which makes up 10% of the xylan polymer by weight, also induces expression of xlnB, although to a lesser extent. Since the effects of arabinose and xylan on induction seem to be additive, it is possible that they cause induction by different mechanisms.

A translation start site and putative signal sequence for the XlnB protein had been suggested based on comparisons of the predicted protein sequence of xlnB with other proteins (26, 33). These predictions, although based entirely on sequence analysis, were completely reasonable. In our analysis of the transcription start site of xlnB, however, we identified an apparent transcription start site within the predicted protein signal sequence. The ability to predict the transcription start site from primer extension analysis relies on the isolation of intact RNA. Primer extension products are used to measure the distance from the point of primer annealing to the 5' end of the RNA molecule isolated, and if the mRNA is partially degraded or processed, the results would be misleading and would not identify the 5' end of the mRNA as it is transcribed. In an attempt to eliminate artifacts that might result from mRNA processing, we used an independent method to determine the transcription start site. In vitro runoff assays rely on the use of partially purified RNA polymerase and a DNA template in an in vitro reaction. RNA polymerization is initiated within a fragment that contains the putative promoter and continues to the end of the fragment. These conditions would presumably eliminate RNA processing events, or, if processing occurred, the products would be detected in the reaction. Since in vitro transcription assays and primer extension analysis of in vivo RNA identified the same transcription start site and since there is no evidence of RNA processing, we conclude that, within the limits of the experimental techniques used, the start site is a G residue well downstream of the previously predicted translation start site. In support of this conclusion is the fact that no runoff transcript was detected when a fragment with this transcription start site deleted was used as the template. If the actual transcription start site were upstream of the translation start site predicted from sequence analysis, we should have detected it in our assays. Although the long protein signal sequence predicted from the DNA sequence appears extremely similar to known signal sequences, if our transcriptional analysis is correct, the actual signal sequence may be much shorter and the translation start site may be an ATG downstream. If this is true, xylanase B may have an 8-amino-acid leader peptide, MLPGTAQA, followed by a signal sequence cleavage site.

While our data for the transcription start site of xlnB are not consistent with the predicted signal sequence proposed previously (26, 33), the results of our experiments are unambiguous and internally consistent. In spite of this, we report them with some caution. The homology between the putative signal sequence of xylanase B and known signal sequences is compelling. We point out that there are no sequences at positions 10 or 35 upstream of the start site we identified that resemble known RNA polymerase recognition sequences, but, given the large number of promoter classes already identified in Streptomyces, this may simply be a new one. Attempts to determine the N-terminal amino acid sequence of XlnB have so far been unsuccessful. Further analysis of the protein sequence of XlnB and identification of cis-acting sequences involved in RNA polymerase recognition and regulation should resolve the questions raised by our analysis.

To define the regulatory region of the promoter of xlnB, deletions of the promoter region were constructed and examined by using transcriptional fusions to the xylE reporter gene. Sequences between 268 and 318 relative to the transcription start site were shown to be required for glucose repression of xylan induction. There are several sequence motifs within this region, including a palindromic sequence, CTTCGAAAtTTTCGgAAG, and three direct-repeat sequences, TTCCGGC, TTCCGGG, and TTCCGCG. Giannotta et al. (14) identified a region of the xlnC promoter that formed complexes with proteins from crude cell extracts in electrophoretic mobility shift assays. This region includes the sequence GAAA-TTTC, which is similar to sequences within the region of the xlnB promoter required for glucose repression. We emphasize that we have no direct evidence that these sequences are important for regulation, and they are implicated only by inspection of the xlnB promoter sequence. Although experiments to elucidate the possible role of these sequences in xlnB regulation are currently in progress in our laboratory, we have not identified bases within the CTTCGAAAtTTTCGgAAG sequence that affect expression or regulation. While this analysis is at an early stage, some base changes in the three direct repeat sequences resulted in decreased levels of xlnB expression. A thorough analysis of these motifs may identify sequences important for regulation.

The use of transcription and localization signals for heterologous gene expression in Streptomyces is also at an early stage of investigation compared with others systems. Streptomyces is a potentially useful host for heterologous expression, especially for the expression of enzymes such as xylanase. Streptomyces is a soil organism that produces and exports a large number of complex-carbohydrate-degrading enzymes, and the use of the expression and localization signals from these enzymes for the production of similar enzymes from other sources is potentially powerful. Xylanase A from T. maritima is an example. The thermostable and pH-stable activity of this enzyme make it well suited for processes such as pulp bleaching, but production of the enzyme from its host, an obligate anaerobe with fastidious growth requirements, would be difficult at best. Our investigation of the expression of this xylanase in Streptomyces clearly shows that the enzyme is expressed and localized and that the activity is thermostable. Our efforts to optimize the system for high-level production, however, are at an early stage. The fact that a promoter deletion that resulted in higher transcription also resulted in higher expression suggests that increased transcription will improve production. Translation of a protein that has a 46% G+C content in an organism that has an overall G+C content of 73% is also likely to present difficulties in translation efficiency due to differences in codon usage. While changing the two TTA codons to CTA had no apparent effect on translation efficiency, the presence of an adenine in the third position (which is 96% guanine or cytosine for most Streptomyces coding regions) may not have been an optimal change. The xynA gene contains several TTT codons, which appear infrequently in Streptomyces. It is clear that a thorough dissection of the rate-limiting steps in production of xylanase A in Streptomyces is needed to address issues of high-level expression.