3.2.1.81: beta-agarase
This is an abbreviated version!
For detailed information about beta-agarase, go to the full flat file.
Word Map on EC 3.2.1.81
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3.2.1.81
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neoagarotetraose
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neoagarobiose
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agarolytic
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neoagarohexaose
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agar-degrading
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pseudoalteromonas
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agarivorans
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atlantica
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microbulbifer
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neoagaro-oligosaccharides
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galactanivorans
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gracilaria
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zobellia
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alteromonas
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catenovulum
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porphyran
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degradans
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saccharophagus
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flammeovirga
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carrageenase
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exo-type
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tat-dependent
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industry
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synthesis
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analysis
- 3.2.1.81
- neoagarotetraose
- neoagarobiose
- agarolytic
- neoagarohexaose
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agar-degrading
- pseudoalteromonas
- agarivorans
- atlantica
- microbulbifer
- neoagaro-oligosaccharides
- galactanivorans
- gracilaria
- zobellia
- alteromonas
- catenovulum
- porphyran
- degradans
-
saccharophagus
- flammeovirga
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carrageenase
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exo-type
-
tat-dependent
- industry
- synthesis
- analysis
Reaction
Synonyms
AGA, Aga21, Aga50D, AgaA, AgaAc, AgaB, AgaB34, AgaC, AgaD, AgaP, agarase, Agarase 0107, agarase AG-a, AgaYT, beta-agarase, beta-agarase A, beta-agarase B, beta-agarase C, beta-agarase D, beta-agarase-a, DagA, endo-type beta-agarase, LSL-1, N3-1 protein, PjaA, RagaA11, YM01-1
ECTree
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Application
Application on EC 3.2.1.81 - beta-agarase
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analysis
industry
synthesis
use of enzyme for preparation of neoagarohexaose and neoagarotetraose and separation of neoagaro-oligosaccharides by consecutive column chromatography
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use of enzyme in agarolysis for recovery of DNA from agarose gels, and use of enzyme as a reporter in the construction of a secretion signal trap, a simple and efficient molecular tool for the selction of genes encoding secretion proteins from both gram-positive and gram-negative bacteria
analysis
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use of enzyme in agarolysis for recovery of DNA from agarose gels, and use of enzyme as a reporter in the construction of a secretion signal trap, a simple and efficient molecular tool for the selction of genes encoding secretion proteins from both gram-positive and gram-negative bacteria
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use of enzyme as a cosmetic additive. The oligosaccharides produced by the enzyme have a whitening effect and inhibit tyrosinase activity in the murine melanoma cell line, B16F10. They are not cytotoxic to B16F10 or normal cells
industry
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approaches for the preparation of a series of neoagaro-oligosaccharides by beta-agarase digestion. This system may be applicable in the production of oligosaccharides by beta-agarase digestion from natural sources such as algae
industry
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creation of a thermostable mutant L122Q/N446I of beta-agarase AgaB by directed evolution. The higher thermostability of mutant L122Q/N446I, in conjunction with its high specific activity and product specificity, will allow this enzyme to have potentials in industrial applications
industry
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use of enzyme as a cosmetic additive. The oligosaccharides produced by the enzyme have a whitening effect and inhibit tyrosinase activity in the murine melanoma cell line, B16F10. They are not cytotoxic to B16F10 or normal cells
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