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(S)-lactate fermentation to propanoate, acetate and hydrogen
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PWY-8086
all-trans-farnesol biosynthesis
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PWY-6859
anapleurotic synthesis of oxalacetate
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apratoxin A biosynthesis
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PWY-8361
arachidonate metabolites biosynthesis
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PWY-8397
Arachidonic acid metabolism
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arachidonic acid metabolism
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avenanthramide biosynthesis
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PWY-8157
bacterial bioluminescence
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PWY-7723
benzoate biosynthesis II (CoA-independent, non-beta-oxidative)
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PWY-6444
Bifidobacterium shunt
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P124-PWY
Biosynthesis of secondary metabolites
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bisabolene biosynthesis (engineered)
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PWY-7102
C20 prostanoid biosynthesis
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PWY66-374
Carbon fixation pathways in prokaryotes
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cinnamoyl-CoA biosynthesis
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PWY-6457
Citrate cycle (TCA cycle)
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curacin A biosynthesis
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PWY-8358
Cysteine and methionine metabolism
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di-homo-gamma-linolenate metabolites biosynthesis
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PWY-8396
ephedrine biosynthesis
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PWY-5883
epoxypseudoisoeugenol-2-methylbutanoate biosynthesis
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PWY-5882
ethene biosynthesis III (microbes)
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PWY-6854
eugenol and isoeugenol biosynthesis
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PWY-5859
farnesene biosynthesis
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PWY-5725
ferrichrome A biosynthesis
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PWY-7571
gluconeogenesis II (Methanobacterium thermoautotrophicum)
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PWY-6142
gluconeogenesis III
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PWY66-399
Glycolysis / Gluconeogenesis
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Glycosaminoglycan degradation
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heterolactic fermentation
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P122-PWY
icosapentaenoate metabolites biosynthesis
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PWY-8399
incomplete reductive TCA cycle
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P42-PWY
isoprene biosynthesis II (engineered)
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PWY-7391
isoprenoid biosynthesis
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ketogenesis
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PWY66-367
L-histidine degradation V
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PWY-5031
L-lactaldehyde degradation
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Methanobacterium thermoautotrophicum biosynthetic metabolism
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PWY-6146
methyl phomopsenoate biosynthesis
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PWY-7721
methylerythritol phosphate pathway I
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NONMEVIPP-PWY
methylerythritol phosphate pathway II
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PWY-7560
methylsalicylate biosynthesis
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PWY18C3-22
mevalonate metabolism
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mevalonate pathway I (eukaryotes and bacteria)
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PWY-922
mevalonate pathway II (haloarchaea)
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PWY-6174
mevalonate pathway III (Thermoplasma)
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PWY-7524
mevalonate pathway IV (archaea)
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PWY-8125
Microbial metabolism in diverse environments
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monoterpene biosynthesis
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PWY-3041
nocardicin A biosynthesis
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PWY-7797
oleandomycin activation/inactivation
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PWY-6972
Phenylalanine metabolism
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phenylethyl acetate biosynthesis
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PWY-7075
Phenylpropanoid biosynthesis
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phenylpropanoid biosynthesis
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phenylpropanoid biosynthesis, initial reactions
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PWY1F-467
Propanoate metabolism
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pyruvate fermentation to (S)-lactate
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PWY-5481
reactive oxygen species degradation
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DETOX1-PWY-1
reductive TCA cycle I
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P23-PWY
rosmarinic acid biosynthesis I
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PWY-5048
rutin degradation (plants)
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PWY-7134
Sesquiterpenoid and triterpenoid biosynthesis
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stellatic acid biosynthesis
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PWY-7736
suberin monomers biosynthesis
superoxide radicals degradation
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DETOX1-PWY
superpathway of glucose and xylose degradation
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PWY-6901
Terpenoid backbone biosynthesis
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trans, trans-farnesyl diphosphate biosynthesis
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PWY-5123
Valine, leucine and isoleucine degradation
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volatile benzenoid biosynthesis I (ester formation)
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PWY-4203
suberin monomers biosynthesis
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PWY-1121
suberin monomers biosynthesis
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flower buds (8 h before flower opening; 12 p.m.) already possesses substantial SAMT enzymatic activity (approximately 22% of peak level). Maximal SAMT activity is observed inmature flower buds i.e., 4 h before petal opening (4 p.m.). After petal opening, the level of activity of SAMT starts declining, and it is almost 78% less than the peak level. SAMT activity in petals again reaches to the second peak level after 8 h of petal opening
brenda
additional information
during the life span of Jasminum sambac flower, clear variations in monoterpene emission between the day and night periods are observed for linalool and beta-ocimene that continue to emituntil next morning
brenda
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brenda
flower buds (8 h before flower opening; 12 p.m.) already possesses substantial SAMT enzymatic activity (approximately 22% of peak level). Maximal SAMT activity is observed inmature flower buds i.e. 4 h before petal opening (4 p.m.). After petal opening, the level of activity of SAMT starts declining, and it is almost 78% less than the peak level. SAMT activity in petals again reaches to the second peak level after 8 h of petal opening
brenda
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highest BAMT enzyme activity is found after 4 h of petal opening i.e., at 12 a.m. of night. Although the first peak is observed at 4 p.m. (4 h before petal opening), after reached at its highest level of activity, BAMT activity gradually decreases as found in the emission of methylbenzoate, where the highest emission is at 2 a.m. of night, i.e. 6 h of petal opening
brenda
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brenda
maximum TPS transcript accumulation is observed in flower petals, analysis of JsTPS expression in different developmental stages and in different floral part by semiquantitative RT-PCR. Unopened flower (buds) emit no beta-ocimene or farnesene. Senescence initiated in Jasminnum sambac flower after 24 h of petal opening, while low emission of linalool and beta-ocimene is detected until the abscission of floral tissue. beta-Ocimene is not detected in any other floral tissue except petals with a very lowamount of emission
brenda