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Basic Ligand Information
Roles as Enzyme Ligand
Enzyme Kinetic Parameters
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Ligand lactobiono-1,5-lactone

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Basic Ligand Information

Molecular Structure

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Molecular Formula

BRENDA Name

InChIKey

C₁₂H₂₀O₁₁

lactobiono-1,5-lactone

FSICMNGKCHFHGP-AMTLMPIISA-N

Synonyms:

4-O-(beta-D-galactopyranosyl)-D-glucono-1,5-lactone, 4-O-beta-D-galactopyranosyl-D-glucono-1,5-lactone, alpha-D-lactono-1,5-lactone, D-lactono-1,5-lactone, lactobiono-lactone, lactono-1,5-lactone

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Roles as Enzyme Ligand

In Vivo Product in Enzyme-catalyzed Reactions (3 results)

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EC NUMBER

PROVEN IN VIVO REACTION

REACTION DIAGRAM

LITERATURE

ENZYME 3D STRUCTURE

1.1.99.18

lactose + acceptor = 4-O-(beta-D-galactopyranosyl)-D-glucono-1,5-lactone + reduced acceptor

1.1.99.29

lactose + acceptor = lactobiono-1,5-lactone + 2-dehydrolactose + 2,3-didehydrolactose + reduced acceptor

1.1.99.35

lactose + oxidized 2,6-dichlorophenolindophenol = lactono-1,5-lactone + reduced 2,6-dichlorophenolindophenol

Product in Enzyme-catalyzed Reactions (37 results)

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EC NUMBER

REACTION

REACTION DIAGRAM

LITERATURE

ENZYME 3D STRUCTURE

1.1.1.47

D-lactose + NAD+ = D-lactono-1,5-lactone + NADH + H+

1.1.5.2

alpha-D-lactose + phenazine methosulfate = alpha-D-lactono-1,5-lactone + reduced phenazine methosulfate

1.1.5.2

D-lactose + 2,6-dichlorophenolindophenol = D-lactono-1,5-lactone + reduced 2,6-dichlorophenolindophenol

1.1.5.2

lactose + 2,6-dichlorophenolindophenol = lactono-1,5-lactone + reduced 2,6-dichlorophenolindophenol

1.1.5.2

3 entries

1.1.5.9

D-lactose + 2,6-dichlorophenolindophenol = D-lactono-1,5-lactone + reduced 2,6-dichlorophenolindophenol

1.1.99.18

lactose + 1,4-benzoquinone = 4-O-(beta-D-galactopyranosyl)-D-glucono-1,5-lactone + 1,4-benzoquinol

1.1.99.18

lactose + 2,6-dichloroindophenol = 4-O-(beta-D-galactopyranosyl)-D-glucono-1,5-lactone + reduced 2,6-dichloroindophenol

1.1.99.18

lactose + 2,6-dichloroindophenol = 4-O-(beta-D-galactopyranosyl)-D-glucono-1,5-lactone + reduced 2,6-dichlorophenolindophenol

1.1.99.18

lactose + 2,6-dichloroindophenol = 4-O-(beta-D-galactopyranosyl)-D-glucono-1,5-lactone + reduced 2,6dichloro-indophenol

1.1.99.18

lactose + 2,6-dichlorophenol indophenol = 4-O-(beta-D-galactopyranosyl)-D-glucono-1,5-lactone + reduced 2,6-dichlorophenol indophenol

1.1.99.18

lactose + 2,6-dichlorophenol indophenol = 4-O-(beta-D-galactopyranosyl)-D-glucono-1,5-lactone + reduced 2,6-dichlorophenolindophenol

1.1.99.18

lactose + 2,6-dichlorophenol-indophenol = 4-O-(beta-D-galactopyranosyl)-D-glucono-1,5-lactone + reduced 2,6-dichlorophenol-indophenol

1.1.99.18

lactose + 3,5-di-tert-butyl-1,2-benzoquinone = 4-O-(beta-D-galactopyranosyl)-D-glucono-1,5-lactone + ?

1.1.99.18

lactose + acceptor = 4-O-(beta-D-galactopyranosyl)-D-glucono-1,5-lactone + reduced acceptor

287783, 287782, 0, 287779, 287784, 287774, 287776, 287780, 287772, 287773

1.1.99.18

lactose + cytochrome c = 4-O-(beta-D-galactopyranosyl)-D-glucono-1,5-lactone + reduced cytochrome c

1.1.99.18

lactose + Fe(CN)63- = 4-O-(beta-D-galactopyranosyl)-D-glucono-1,5-lactone + Fe(CN)64-

1.1.99.18

lactose + ferricenium ion = 4-O-(beta-D-galactopyranosyl)-D-glucono-1,5-lactone + ?

1.1.99.18

lactose + ferricytochrome c = 4-O-(beta-D-galactopyranosyl)-D-glucono-1,5-lactone + ferrocytochrome c

1.1.99.18

lactose + K3Fe(CN)6 = 4-O-(beta-D-galactopyranosyl)-D-glucono-1,5-lactone + reduced K3Fe(CN)6

1.1.99.18

lactose + methylene blue = 4-O-(beta-D-galactopyranosyl)-D-glucono-1,5-lactone + reduced methylene blue

1.1.99.18

lactose + O2 = 4-O-(beta-D-galactopyranosyl)-D-glucono-1,5-lactone + H2O2

0, 389750, 389753

1.1.99.18

beta-D-lactose + benzoquinone = lactobiono-1,5-lactone + benzoquinol

1.1.99.18

lactose + 2,6-dichlorophenol indophenol = lactobiono-1,5-lactone + reduced 2,6-dichlorophenol indophenol

1.1.99.18

lactose + 2,6-dichlorophenol-indophenol = lactobiono-1,5-lactone + ?

1.1.99.18

lactose + 2,6-dichlorophenolindophenol = lactobiono-1,5-lactone + ?

1.1.99.18

lactose + acceptor = lactobiono-1,5-lactone + reduced acceptor

1.1.99.18

lactose + cytochrome c = lactobiono-1,5-lactone + reduced cytochrome c

1.1.99.18

lactose + 2,6-dichlorophenolindophenol = lactono-1,5-lactone + reduced 2,6-dichlorophenolindophenol

1.1.99.18

lactose + cytochrome c = lactono-1,5-lactone + reduced cytochrome c

1.1.99.18

lactose + ferricytochrome c = lactono-1,5-lactone + ferrocytochrome c

1.1.99.29

lactose + acceptor = lactobiono-1,5-lactone + 2-dehydrolactose + 2,3-didehydrolactose + reduced acceptor

1.1.99.29

lactose + acceptor = lactobiono-1,5-lactone + reduced acceptor

1.1.99.35

lactose + oxidized N-methylphenazonium methyl sulfate = 4-O-beta-D-galactopyranosyl-D-glucono-1,5-lactone + reduced N-methylphenazonium methyl sulfate

1.1.99.35

lactose + 1-(N,N-dimethylamine)-4-(4-morpholine)benzene = lactono-1,5-lactone + reduced 1-(N,N-dimethylamine)-4-(4-morpholine)benzene

1.1.99.35

lactose + N,N'-dimethyl-4,4'-azopyridinium methyl sulfate = lactono-1,5-lactone + reduced N,N'-dimethyl-4,4'-azopyridinium methyl sulfate

1.1.99.35

lactose + N-methylphenazonium methylsulfate = lactono-1,5-lactone + reduced N-methylphenazonium methylsulfate

1.1.99.35

lactose + oxidized 2,6-dichlorophenolindophenol = lactono-1,5-lactone + reduced 2,6-dichlorophenolindophenol

Inhibitor in Enzyme-catalyzed Reactions (1 result)

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EC NUMBER

COMMENTARY

LITERATURE

ENZYME 3D STRUCTURE

1.1.99.18

weak product inhibition

287787

Enzyme Kinetic Parameters

K_i Value (1 result)

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EC NUMBER

KI VALUE [MM]

KI VALUE MAXIMUM [MM]

COMMENTARY

LITERATURE

1.1.99.18

287787

References & Links

Literature References (12)

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Show Reference (12 entries)

BRENDA REFERENCE ID

PUBMED ID

TITLE

YEAR

AUTHORS

JOURNAL

VOLUME

PAGES

287772

Induction and characterization of a cellobiose dehydrogenase produced by a species of Monilia

1980

Dekker, R.F.H.

J. Gen. Microbiol.

120

309-316

287773

Cellobiose dehydrogenase produced by Monilia sp.

1988

Dekker, R.F.H.

Methods Enzymol.

160

454-463

287774

The purification and properties of cellobiose dehydrogenase from Sclerotium rolfsii and its role in cellulolysis

1985

Sadana, J.C.; Patil, R.V.

J. Gen. Microbiol.

131

1917-1923

287776

7103940

Characterization of a cellobiose dehydrogenase in the cellulolytic fungus Sporotrichum (Chrysosporium) thermophile

1982

Coudray, M.R.; Canevascini, G.; Meier, H.

Biochem. J.

203

277-284

287779

8434950

Purification and characterization of cellobiose dehydrogenase, a novel extracellular hemoflavoenzyme from the white-rot fungus Phanerochoaete chrysosporium

1993

Bao, W.; Usha, S.N.; Renganathan, V.

Arch. Biochem. Biophys.

300

705-713

287780

8434937

Isolation and characterization of the cellobiose dehydrogenase from brown-rot fungus Coniophora puteana (Schum ex Fr.)Karst.

1993

Schmidhalter, D.R.; Canevascini, G.

Arch. Biochem. Biophys.

300