The present study investigated the efficiency of Aspergillus sydowii strain bpol(GenBank Accession Number:MK373021)in the removal of anthracene(100 mg/L).Optimal degradation efficiency(98.7%)was observed at neutral pH...The present study investigated the efficiency of Aspergillus sydowii strain bpol(GenBank Accession Number:MK373021)in the removal of anthracene(100 mg/L).Optimal degradation efficiency(98.7%)was observed at neutral pH,temperature(30℃),biomass weight(2 g)and salinity(0.2%w/v)within 72 h.The enzyme analyses revealed 131%,107%,and 89%induction in laccase,lignin peroxidase,and manganese peroxidase respectively during anthracene degradation.Furthermore,the degradation efficiency(99.8%)and enzyme induction were significantly enhanced with the addition of 100 mg/L of citric acid and glucose to the culture.At varying anthracene concentrations(100-500 mg/L),the degradation rate constants(K1)peaked with increasing concentration of anthracene while the half-life(t1/2)decreases with increase in anthracene concentration.Goodness of fit(R2=0.976 and 0.982)was observed when the experimental data were subjected to Langmuir and Temkin models respectively which affirmed the monolayer and heterogeneous nature exhibited by A.sydwoii cells during degradation.Four distinct metabolites;anthracene-1,8,9(2H,8aH,9aH)-trione,2,4adihydronaphthalene-1,5-dione,l,3,3a,7a-tetrahydro-2-benzofuran-4,7-dione and 2-hydroxybenzoic acid was obtained through Gas Chromatography-Mass spectrometry(GC-MS).A.sydowii exhibited promising potentials in the removal of PAHs.展开更多
基金Bankole Paul Olusegun hereby thank the Association of Commonwealth Universities(ACU)for the 2019 Blue Charter Award.
文摘The present study investigated the efficiency of Aspergillus sydowii strain bpol(GenBank Accession Number:MK373021)in the removal of anthracene(100 mg/L).Optimal degradation efficiency(98.7%)was observed at neutral pH,temperature(30℃),biomass weight(2 g)and salinity(0.2%w/v)within 72 h.The enzyme analyses revealed 131%,107%,and 89%induction in laccase,lignin peroxidase,and manganese peroxidase respectively during anthracene degradation.Furthermore,the degradation efficiency(99.8%)and enzyme induction were significantly enhanced with the addition of 100 mg/L of citric acid and glucose to the culture.At varying anthracene concentrations(100-500 mg/L),the degradation rate constants(K1)peaked with increasing concentration of anthracene while the half-life(t1/2)decreases with increase in anthracene concentration.Goodness of fit(R2=0.976 and 0.982)was observed when the experimental data were subjected to Langmuir and Temkin models respectively which affirmed the monolayer and heterogeneous nature exhibited by A.sydwoii cells during degradation.Four distinct metabolites;anthracene-1,8,9(2H,8aH,9aH)-trione,2,4adihydronaphthalene-1,5-dione,l,3,3a,7a-tetrahydro-2-benzofuran-4,7-dione and 2-hydroxybenzoic acid was obtained through Gas Chromatography-Mass spectrometry(GC-MS).A.sydowii exhibited promising potentials in the removal of PAHs.
