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4-hydroxy-2-nonenal detoxification
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PWY-7112
5-oxo-L-proline metabolism
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PWY-7942
allantoin degradation
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allantoin degradation to glyoxylate I
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PWY-5694
allantoin degradation to glyoxylate III
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PWY-5705
Amino sugar and nucleotide sugar metabolism
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Arginine and proline metabolism
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Ascorbate and aldarate metabolism
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beta-(1,4)-mannan degradation
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PWY-7456
beta-D-glucuronide and D-glucuronate degradation
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PWY-7247
Biosynthesis of secondary metabolites
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camalexin biosynthesis
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CAMALEXIN-SYN
chondroitin sulfate degradation I (bacterial)
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PWY-6572
creatine phosphate biosynthesis
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PWY-6158
D-galacturonate degradation I
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GALACTUROCAT-PWY
degradation of sugar acids
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dermatan sulfate degradation I (bacterial)
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PWY-7646
Drug metabolism - cytochrome P450
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Drug metabolism - other enzymes
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ethanol degradation IV
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PWY66-162
Flavone and flavonol biosynthesis
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fructan degradation
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PWY-862
Fructose and mannose metabolism
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gellan degradation
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PWY-6827
gliotoxin biosynthesis
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PWY-7533
Glutathione metabolism
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glutathione metabolism
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glutathione-mediated detoxification I
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PWY-4061
glutathione-mediated detoxification II
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PWY-6842
Glycerolipid metabolism
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Glycosaminoglycan degradation
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Glyoxylate and dicarboxylate metabolism
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heparan sulfate degradation
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PWY-7651
heparin degradation
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PWY-7644
hyaluronan degradation
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PWY-7645
indole glucosinolate activation (intact plant cell)
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PWYQT-4477
L-leucine degradation I
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LEU-DEG2-PWY
luteolin triglucuronide degradation
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PWY-7445
Metabolism of xenobiotics by cytochrome P450
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methanol oxidation to formaldehyde IV
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PWY-5506
N-acetylneuraminate and N-acetylmannosamine degradation II
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PWY-7581
nocardicin A biosynthesis
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PWY-7797
Other glycan degradation
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pectin degradation II
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PWY-7248
pentachlorophenol degradation
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PCPDEG-PWY
Pentose and glucuronate interconversions
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Porphyrin and chlorophyll metabolism
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reactive oxygen species degradation
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DETOX1-PWY-1
Sphingolipid metabolism
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Steroid hormone biosynthesis
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sulfated glycosaminoglycan metabolism
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superoxide radicals degradation
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DETOX1-PWY
triacylglycerol degradation
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LIPAS-PWY
Tryptophan metabolism
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Valine, leucine and isoleucine degradation
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2620, 5972, 5974, 5976, 5977, 5979, 5980, 5981, 5982, 5984, 5985, 5986, 34081, 34082, 34086, 34089, 34090, 34091, 34093, 34100, 34101, 34103, 37404, 37406, 37407, 37408, 37409, 37410, 37412, 136629, 136631, 170832, 288765, 649318, 649969, 650383, 650773, 651587, 651971, 652640, 653976, 664047, 664524, 664604, 665449, 665613, 677405, 677536, 680938, 681056, 681722, 682098, 690418, 692532, 693981, 701659, 701676, 704598, 704673, 706673, 714027, 715037, 715131, 729521, 730368, 730873, 747335, 747363, 747454, 747455, 747456, 747533, 747570
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brenda
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SwissProt
brenda
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UniProt
brenda
ATCC 13125
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brenda
formerly Flavobacterium heparinum
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brenda
gene cAC
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brenda
gene cslA
SwissProt
brenda
gene Phep_2238
UniProt
brenda
gene Phep_2649
UniProt
brenda
gene Phep_2830
UniProt
brenda
gram-negative soil bacterium, also known as Cythophaga heparinia
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brenda
i.e. Cytophaga heparina, Sphingobacterium heparinum, or Pedobacter heparinus, gene cslB
SwissProt
brenda
i.e. Cytophaga heparinia
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brenda
i.e. Flavobacterium heparinum
SwissProt
brenda
isoform chondroitinase AC, upon growth on peptone with or without the inducer chondroitin sulfate, high specific activities for chondroitinases during the initial 6 h, which decreased thereafter. In contrast, in tryptic soy broth, high specific activities were obtained after 24 h growth in the presence of the inducer, generating large amounts of chondroitinase-rich extracts
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brenda
isoform chondroitinase B, upon growth on peptone with or without the inducer chondroitin sulfate, high specific activities for chondroitinases during the initial 6 h, which decreased thereafter. In contrast, in tryptic soy broth, high specific activities were obtained after 24 h growth in the presence of the inducer, generating large amounts of chondroitinase-rich extracts
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brenda
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optimization of enzyme production, simple carbon sources, including sucrose, lactose, maltose, and complex carbon sources such as starch and cellulose are able to support growth of the organism, but enzyme can be produced only in the presence of maltose, sorbitol, mannitol, arabinose, and mannose. Phosphate inhibits enzyme production and cell growth, while heparin inhibits cell growth but is required for enzyme induction, overview. Heparinase production in optimized medium is highest, i.e., 75.4 units, when the pH of the medium is kept at pH 6.5, inoculum size of 0.5-1.0% of spore suspension, and for an incubation temperature of 30°C. Growth profile, heparin utilization, and heparinase production in optimized medium, overview
brenda
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brenda
additional information
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propagated in bovine lung microvascular endothelial cells
brenda
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