Degradation of toluene by ortho cleavage enzymes in Burkholderia fungorum FLU100
Summary Burkholderia fungorum FLU100 simultaneously oxidized any mixture of toluene, benzene and mono‐halogen benzenes to (3‐substituted) catechols with a selectivity of nearly 100%. Further metabolism occurred via enzymes of ortho cleavage pathways with complete mineralization. During the transform...
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Published in | Microbial biotechnology Vol. 8; no. 1; pp. 143 - 154 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
United States
BlackWell Publishing Ltd
01.01.2015
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Subjects | |
Online Access | Get full text |
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Summary: | Summary
Burkholderia fungorum FLU100 simultaneously oxidized any mixture of toluene, benzene and mono‐halogen benzenes to (3‐substituted) catechols with a selectivity of nearly 100%. Further metabolism occurred via enzymes of ortho cleavage pathways with complete mineralization. During the transformation of 3‐methylcatechol, 4‐carboxymethyl‐2‐methylbut‐2‐en‐4‐olide (2‐methyl‐2‐enelactone, 2‐ML) accumulated transiently, being further mineralized only after a lag phase of 2 h in case of cells pre‐grown on benzene or mono‐halogen benzenes. No lag phase, however, occurred after growth on toluene. Cultures inhibited by chloramphenicol after growth on benzene or mono‐halogen benzenes were unable to metabolize 2‐ML supplied externally, even after prolonged incubation. A control culture grown with toluene did not show any lag phase and used 2‐ML as a substrate. This means that 2‐ML is an intermediate of toluene degradation and converted by specific enzymes. The conversion of 4‐methylcatechol as a very minor by‐product of toluene degradation in strain FLU100 resulted in the accumulation of 4‐carboxymethyl‐4‐methylbut‐2‐en‐4‐olide (4‐methyl‐2‐enelactone, 4‐ML) as a dead‐end product, excluding its nature as a possible intermediate. Thus, 3‐methylcyclohexa‐3,5‐diene‐1,2‐diol, 3‐methylcatechol, 2‐methyl muconate and 2‐ML were identified as central intermediates of productive ortho cleavage pathways for toluene metabolism in B. fungorum FLU100.
Burkholderia fungorum FLU100 simultaneously oxidised any mixture of toluene, benzene and mono‐halogen benzenes to (3‐substituted) catechols with a selectivity of nearly 100 % and mineralises these catechols by enzymes of the ortho cleavage pathway. During the transformation of 3‐methylcatechol, 4‐carboxymethyl‐2‐methylbut‐2‐en‐4‐olide (2‐methyl‐2‐enelactone, 2‐ML) accumulated transiently, being further mineralised only after a lag‐phase of 2 h in case of cells pre‐grown on benzene or mono‐halogen benzenes. No lag‐phase, however, occurred after growth on toluene. |
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Bibliography: | Funding Information This work was supported by grant EN 474/2-2 from the Deutsche Forschungsgemeinschaft (DFG). |
ISSN: | 1751-7915 1751-7915 |
DOI: | 10.1111/1751-7915.12147 |