The pathway with the name m-Cresol
 has the following structure: 
Result: 
C1=CC(=CC(=C1)C(=O)[O-])O
 SimpleRule(uri = https://envipath.org/package/32de3cf4-e3e6-4168-956e-32fa5ddb0ce1/simple-rule/d2c05443-dde1-4fe3-96e4-0e99517a00ed, SMIRKS = [H][c:1]1[c:8][#6,#7;a:7][c:6][c:5][c:4]1-[#8;!$([O;H1]c1cccc([O;H1])c1):9][H]>>[#8:9]([H])-[c:4]1[c:5][c:6][#6,#7;a:7][c:8][c:1]1-[#8]([H])) C1=C(C=C(C(=C1)O)O)C(=O)[O-]
C1=CC(=CC(=C1)CO)O
 SimpleRule(uri = https://envipath.org/package/32de3cf4-e3e6-4168-956e-32fa5ddb0ce1/simple-rule/24d3215b-aefa-4538-b345-16e2a5e042b1, SMIRKS = [H][#8:2][C:1]([H:5])([H])[#1,#6:6]>>[H:5][#6:1](-[#1,#6:6])=[O:2]) C1=CC(=CC(=C1)C=O)O
C1=CC(=CC(=C1)C=O)O
 SimpleRule(uri = https://envipath.org/package/32de3cf4-e3e6-4168-956e-32fa5ddb0ce1/simple-rule/737ec046-645e-46ec-af34-c44500fe5899, SMIRKS = [H][#6:1](-[#6:5])=[O:4]>>[#6:5]-[#6:1](-[#8-])=[O:4]) C1=CC(=CC(=C1)C(=O)[O-])O
C1=CC(=CC(=C1)C(=O)[O-])O
 SimpleRule(uri = https://envipath.org/package/32de3cf4-e3e6-4168-956e-32fa5ddb0ce1/simple-rule/f2d84038-66a1-44cb-a73e-946a9d7c9115, SMIRKS = [H:10][#8:9]-[c:4]1[c;R1:5][c;R1:6][c:1]([H])[c;R1:7][c;R1:8]1>>[H:10][#8:9]-[c:4]1[c;R1:5][c;R1:6][c:1](-[#8])[c;R1:7][c;R1:8]1) C1=C(C=C(C(=C1)O)C(=O)[O-])O
CC1=CC=CC(=C1)O
 no rule associatedC1=CC(=CC(=C1)CO)O

Description: Cresol is a mixture of o-, p-, and m-cresol, and is obtained from coal tar or petroleum. These isomers are used as a disinfectants, textile scouring agents, surfactants and as intermediates in the manufacture of salicylaldehyde, coumarin, and herbicides. Creosote is a less refined petrochemical mixture containing cresol. It is used as a fungicide and a wood preservative for railroad ties, telephone poles, and marine pilings. Despite their chemical similarity, cresol isomers are degraded by bacteria through different pathways. One intermediate in this pathway, 3-hydroxybenzyl alcohol, is also an intermediate in the biosynthetic pathway of patulin ([http://www.ncbi.nlm.nih.gov/pubmed/6988382|Grootwassink & Gaucher, 1980]), a toxin and antiviral agent produced by some molds such as Penicillium patulinum. When grown on m-cresol as a sole carbon source, P. putida 9869 metabolizes the compound via the meta pathway with 3-methylcatechol as an intermediate ([http://www.ncbi.nlm.nih.gov/pubmed/1123316|Hopper et al., 1975]). It has been shown that Pseudomonas picketti also degrade m-cresol via 3-methylcatechol, as presented in the Toluene Pathway ([http://www.ncbi.nlm.nih.gov/pubmed/1892384|Shields et al., 1991]). [http://www.ncbi.nlm.nih.gov/pubmed/1123316|Hopper and Taylor (1974)] have also reported that P. putida 9869, when grown on 3,5-xylenol as a sole carbon source, metabolizes m-cresol via the gentisate pathway, as depicted in this text map. The genes coding for these enzymes are believed to be contained on a plasmid larger than the TOL plasmid which codes enzymes capable of degrading a many aromatic compounds ([http://www.ncbi.nlm.nih.gov/pubmed/6989805|Hopper et al., 1980]).
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