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A system, such as a gap drying system, moves a substrate having a substrate tension over a curved plate at a substrate speed such that the substrate floats over at least a region of substantially constant clearance (H0) between the substrate and the curved plate. H0is controlled without adjusting th

A system, such as a gap drying system, moves a substrate having a substrate tension over a curved plate at a substrate speed such that the substrate floats over at least a region of substantially constant clearance (H0) between the substrate and the curved plate. H0is controlled without adjusting the substrate speed and without adjusting the substrate tension.

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A system, such as a gap drying system, moves a substrate having a substrate tension over a curved plate at a substrate speed such that the substrate floats over at least a region of substantially constant clearance (H0) between the substrate and the curved plate. H0is controlled without adjusting th

A system, such as a gap drying system, moves a substrate having a substrate tension over a curved plate at a substrate speed such that the substrate floats over at least a region of substantially constant clearance (H0) between the substrate and the curved plate. H0is controlled without adjusting the substrate speed and without adjusting the substrate tension. ). Kumagae et al., "Conversion of Starch to Ethanol in a Recombinant Saccharomyces cerevisiae Strain Expressing Rice α-amylase from a Novel Pichia pastoris Alcohol Oxidase Promoter," Biotechnology 11:606-610 (1993). Van Hartingsveldt et al., "Cloning, Characterization and Overexpression of the Phytase-Encoding Gene (phyA) of Aspergillus niger," Gene 127:87-94 (1993). Phillippy et al., "Expression of an Aspergillus niger Phytase (phyA) in Escherichia coli," J. Agric Food Chem. 45(8):3337-3342 (1997). Rodriquez et al., "Site-Directed Mutagenesis Improves Catalytic Efficiency and Thermostability of Escherichia coli pH 2.5 Acid Phosphatase/Phytase Expressed in Pichia pastoris," Archives of Biochemistry and Biophysics 382(1):105-112 (2000). Boer et al., "Characterization of Trichoderma reesei Cellobiohydrolase Cel7a Secreted from Pichia pastoris Using Two Different Promoters," Biotechnology and Bioengineering 69(5):486-494 (2000). Takahashi et al., "Independent Production of Two Moleclar Forms of a Recombinant Rhizopus oryae Lipase by KEX2-Engineered Strains of Saccharomyces cerevisiae," Applied Microbiol. Biotechnology, 52(4):534-540 (1999). Meldgaard et al., "Different Effects of N-Glycosylation on the Thermostability of Highly Homologous Bacterial (1,3-1,4)-β-Glucanases Secreted from Yeast," Microbiology 140(1):159-166 (1994). Kanai et al., "Recombinant Thermostable Cycloinulo-oligosaccharide Fructanotransferase Produced by Saccharomyces cerevisiae," Appl. Environ. Microbiol. 63(12):4956-4960 (1997). Terashima et al., "The Roles of the N-Linked Carbohydrate Chain of Rice α-amylase in Thermostability and Enzyme Kinetics," Eur. J. Biochem. 226:249-254 (1994). Atlung et al., "Role of the Transcriptional Activator AppY in Regulation of the cyx appA Operon of Escherichia coli by Anaerobiosis, Phosphate Starvation, and Growth Phase," Journal of Bacteriology 176(17):5414-5422 (1994). Belin et al., "A Pleiotropic Acid Phosphatase-Deficient Mutant of Excherichia coli Shows Premature Termination in the dsbA Gene. Use of dsbA::phoA Fusions to Localize a Structurally Important Domain in DsbA," Mol. Gen. Genet. 242:23-32 (1994). Dassa et al., "Indentification of the Gene appA for the Acid Phosphatase (pH Optimum 2.5) of Escherichia coli," Mol. Gen. Genet., 200:68-73 (1985). Piddington et al., "The Cloning and Sequencing of the Genes Encoding Phytase (phy) and pH 2.5-Optimum Acid Phosphatase (aph) from Aspergillus niger var. awamori," Gene, 133:55-62 (1993). Jia et al, "Purification, Crystallization and Preliminary X-ray Analysis of the Escherichia coli Phytase," Acta Cryst., D54:647-649 (1998). Kim et al., "Cloning of the Thermostable Phytase Gene (phy) from Bacillus sp. DS11 and its Overexpression in Escherichia coli," FEMS Microbiology Letters, 162:185-191 (1998). Kerovuo et al., "Isolation, Characterization, Molecular Gene Cloning, and Sequencing of a Novel Phytase from Bacillus subtilis," Applied and Environmental Microbiology, 64(6):2079-2085 (1998). Wyss et al., "Biophysical Characterization of Fungal Phytases (myo-Inositol Hexakisphosphate Phosphohydrolases): Molecular Size, Glycosylation Pattern, and Engineering of Proteolytic Resistance," Applied and Environment Microbiology, 65(2):359-366 (1999). Wyss et al., "Biochemical Characterization of Fungal Phytases (myo-Inositol Hexakisphosphate Phosphohydrolases): Catalytic Properties," Applied and Environmental Microbiology, 65(2):367-373 (1999). Han et al., "Role of Glycosylation in the Functional Expression of an Aspergillus niger Phytase (phyA) in Pichia pastoris," Archives of Biochemistry and Biophysics 364(1):83-90 (1999). Rodriguez et al., "Different Sensitivity of Recombinant Aspergillus niger Phytase (r-PhyA) and Escherichia coli pH 2.5 Acid Phosphatase (r-AppA) to Trypsin and Pepsin in Vitro," Archives of Biochemistry and Biophysics 365(2):262-267 (1999). Rodriquez et al., "Cloning, Sequencing, and Expression of an Escherichia coli Acid Phosphatase/Phytas