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Literature summary extracted from

  • Kumar, V.; Chandra, R.
    Characterisation of manganese peroxidase and laccase producing bacteria capable for degradation of sucrose glutamic acid-Maillard reaction products at different nutritional and environmental conditions (2018), World J. Microbiol. Biotechnol., 34, 32 .
    View publication on PubMedView publication on EuropePMC

Natural Substrates/ Products (Substrates)

EC Number Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
1.11.1.13 2 Mn(II) + 2 H+ + H2O2 Klebsiella aerogenes
-
2 Mn(III) + 2 H2O
-
?
1.11.1.13 2 Mn(II) + 2 H+ + H2O2 Enterobacter cloacae
-
2 Mn(III) + 2 H2O
-
?
1.11.1.13 2 Mn(II) + 2 H+ + H2O2 Klebsiella pneumoniae
-
2 Mn(III) + 2 H2O
-
?
1.11.1.13 2 Mn(II) + 2 H+ + H2O2 Salmonella enterica
-
2 Mn(III) + 2 H2O
-
?

Organism

EC Number Organism UniProt Comment Textmining
1.11.1.13 Enterobacter cloacae
-
-
-
1.11.1.13 Klebsiella aerogenes
-
-
-
1.11.1.13 Klebsiella pneumoniae
-
-
-
1.11.1.13 Salmonella enterica
-
-
-

Substrates and Products (Substrate)

EC Number Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
1.11.1.13 2 Mn(II) + 2 H+ + H2O2
-
Klebsiella aerogenes 2 Mn(III) + 2 H2O
-
?
1.11.1.13 2 Mn(II) + 2 H+ + H2O2
-
Enterobacter cloacae 2 Mn(III) + 2 H2O
-
?
1.11.1.13 2 Mn(II) + 2 H+ + H2O2
-
Klebsiella pneumoniae 2 Mn(III) + 2 H2O
-
?
1.11.1.13 2 Mn(II) + 2 H+ + H2O2
-
Salmonella enterica 2 Mn(III) + 2 H2O
-
?

Synonyms

EC Number Synonyms Comment Organism
1.11.1.13 MnP
-
Klebsiella aerogenes
1.11.1.13 MnP
-
Enterobacter cloacae
1.11.1.13 MnP
-
Klebsiella pneumoniae
1.11.1.13 MnP
-
Salmonella enterica

Temperature Optimum [°C]

EC Number Temperature Optimum [°C] Temperature Optimum Maximum [°C] Comment Organism
1.11.1.13 37
-
assay at Enterobacter cloacae
1.11.1.13 37
-
assay at Klebsiella aerogenes
1.11.1.13 37
-
assay at Klebsiella pneumoniae
1.11.1.13 37
-
assay at Salmonella enterica

pH Optimum

EC Number pH Optimum Minimum pH Optimum Maximum Comment Organism
1.11.1.13 7
-
assay at Klebsiella aerogenes
1.11.1.13 7
-
assay at Enterobacter cloacae
1.11.1.13 7
-
assay at Klebsiella pneumoniae
1.11.1.13 7
-
assay at Salmonella enterica

Cofactor

EC Number Cofactor Comment Organism Structure
1.11.1.13 heme
-
Klebsiella aerogenes
1.11.1.13 heme
-
Enterobacter cloacae
1.11.1.13 heme
-
Klebsiella pneumoniae
1.11.1.13 heme
-
Salmonella enterica

General Information

EC Number General Information Comment Organism
1.11.1.13 evolution DNA sequence comparisons and phylogenetic analysis and tree Klebsiella aerogenes
1.11.1.13 evolution DNA sequence comparisons and phylogenetic analysis and tree Enterobacter cloacae
1.11.1.13 evolution DNA sequence comparisons and phylogenetic analysis and tree Klebsiella pneumoniae
1.11.1.13 evolution DNA sequence comparisons and phylogenetic analysis and tree Salmonella enterica
1.11.1.13 additional information GS-MS analysis of organic compounds and products in the ethyl acetate extracted untreated and bacterially-treated sucrose glutamic acid-Maillard reaction products (SGA-MRPs) solution, overview Klebsiella aerogenes
1.11.1.13 additional information GS-MS analysis of organic compounds and products in the ethyl acetate extracted untreated and bacterially-treated sucrose glutamic acid-Maillard reaction products (SGA-MRPs) solution, overview Enterobacter cloacae
1.11.1.13 additional information GS-MS analysis of organic compounds and products in the ethyl acetate extracted untreated and bacterially-treated sucrose glutamic acid-Maillard reaction products (SGA-MRPs) solution, overview Klebsiella pneumoniae
1.11.1.13 additional information GS-MS analysis of organic compounds and products in the ethyl acetate extracted untreated and bacterially-treated sucrose glutamic acid-Maillard reaction products (SGA-MRPs) solution, overview Salmonella enterica
1.11.1.13 physiological function a potential aerobic bacterial consortium is identified consisting of Klebsiella pneumoniae (KU726953), Salmonella enterica (KU726954), Enterobacter aerogenes (KU726955), Enterobacter cloaceae (KU726957) that show optimum production of maganese peroxidase (MnP) and laccase at 120 and 144 h of growth, respectively. The bacterial consortium causes decolourisation of Maillard reactions products (MRPs) up to 70% in presence of glucose (1%), peptone (0.1%) at optimum pH (8.1), temperature (37°C) and shaking speed (180 rpm) within 192 h of incubation, method optimization and evaluation, overview. The reduction of colour of sucrose glutamic acid-Maillard reaction products (SGA-MRPs) correlates with shifting of absorption peaks in UV-Vis spectrophotometry analysis. Further, the changing of functional group in FT-IR data shows appearance of new peaks and GC-MS analysis of degraded sample revealed the depolymerisation of complex MRPs. Maillard reactions products (MRPs) are a major colorant of distillery effluent. They are a major source of environmental pollution due to their complex structures and recalcitrant nature. The toxicity evaluation using seed of Phaseolus mungo L. reveals a reduction of toxicity of MRPs after bacterial treatment Klebsiella aerogenes
1.11.1.13 physiological function a potential aerobic bacterial consortium is identified consisting of Klebsiella pneumoniae (KU726953), Salmonella enterica (KU726954), Enterobacter aerogenes (KU726955), Enterobacter cloaceae (KU726957) that show optimum production of maganese peroxidase (MnP) and laccase at 120 and 144 h of growth, respectively. The bacterial consortium causes decolourisation of Maillard reactions products (MRPs) up to 70% in presence of glucose (1%), peptone (0.1%) at optimum pH (8.1), temperature (37°C) and shaking speed (180 rpm) within 192 h of incubation, method optimization and evaluation, overview. The reduction of colour of sucrose glutamic acid-Maillard reaction products (SGA-MRPs) correlates with shifting of absorption peaks in UV-Vis spectrophotometry analysis. Further, the changing of functional group in FT-IR data shows appearance of new peaks and GC-MS analysis of degraded sample revealed the depolymerisation of complex MRPs. Maillard reactions products (MRPs) are a major colorant of distillery effluent. They are a major source of environmental pollution due to their complex structures and recalcitrant nature. The toxicity evaluation using seed of Phaseolus mungo L. reveals a reduction of toxicity of MRPs after bacterial treatment Enterobacter cloacae
1.11.1.13 physiological function a potential aerobic bacterial consortium is identified consisting of Klebsiella pneumoniae (KU726953), Salmonella enterica (KU726954), Enterobacter aerogenes (KU726955), Enterobacter cloaceae (KU726957) that show optimum production of maganese peroxidase (MnP) and laccase at 120 and 144 h of growth, respectively. The bacterial consortium causes decolourisation of Maillard reactions products (MRPs) up to 70% in presence of glucose (1%), peptone (0.1%) at optimum pH (8.1), temperature (37°C) and shaking speed (180 rpm) within 192 h of incubation, method optimization and evaluation, overview. The reduction of colour of sucrose glutamic acid-Maillard reaction products (SGA-MRPs) correlates with shifting of absorption peaks in UV-Vis spectrophotometry analysis. Further, the changing of functional group in FT-IR data shows appearance of new peaks and GC-MS analysis of degraded sample revealed the depolymerisation of complex MRPs. Maillard reactions products (MRPs) are a major colorant of distillery effluent. They are a major source of environmental pollution due to their complex structures and recalcitrant nature. The toxicity evaluation using seed of Phaseolus mungo L. reveals a reduction of toxicity of MRPs after bacterial treatment Klebsiella pneumoniae
1.11.1.13 physiological function a potential aerobic bacterial consortium is identified consisting of Klebsiella pneumoniae (KU726953), Salmonella enterica (KU726954), Enterobacter aerogenes (KU726955), Enterobacter cloaceae (KU726957) that show optimum production of maganese peroxidase (MnP) and laccase at 120 and 144 h of growth, respectively. The bacterial consortium causes decolourisation of Maillard reactions products (MRPs) up to 70% in presence of glucose (1%), peptone (0.1%) at optimum pH (8.1), temperature (37°C) and shaking speed (180 rpm) within 192 h of incubation, method optimization and evaluation, overview. The reduction of colour of sucrose glutamic acid-Maillard reaction products (SGA-MRPs) correlates with shifting of absorption peaks in UV-Vis spectrophotometry analysis. Further, the changing of functional group in FT-IR data shows appearance of new peaks and GC-MS analysis of degraded sample revealed the depolymerisation of complex MRPs. Maillard reactions products (MRPs) are a major colorant of distillery effluent. They are a major source of environmental pollution due to their complex structures and recalcitrant nature. The toxicity evaluation using seed of Phaseolus mungo L. reveals a reduction of toxicity of MRPs after bacterial treatment Salmonella enterica