Organism	Strain	Reference(s)	Comment(s)
Acinetobacter baylyi	ADP1	Salvachúa, D., Karp, E. M., Nimlos, C. T., Vardon, D. R., & Beckham, G. T. (2015). Towards lignin consolidated bioprocessing: simultaneous lignin depolymerization and product generation by bacteria. Green Chemistry, 17(11), 4951–4967. https://doi.org/10.1039/c5gc01165e; Fischer, R., Bleichrodt, F. S., & Gerischer, U. C. (2008). Aromatic degradative pathways in Acinetobacter baylyi underlie carbon catabolite repression. Microbiology, 154(10), 3095–3103. https://doi.org/10.1099/mic.0.2008/016907-0	-
Klebsiella pneumoniae	M5a1	Jones, D. C. N., & Cooper, R. A. (1990). Catabolism of 3-hydroxybenzoate by the gentisate pathway in Klebsiella pneumoniae M5a1. Archives of Microbiology, 154(5), 489–495. https://doi.org/10.1007/bf00245233	-
Rhodococcus opacus	DSM 1069	Kosa, M., & Ragauskas, A. J. (2011). Bioconversion of lignin model compounds with oleaginous Rhodococci. Applied Microbiology and Biotechnology, 93(2), 891–900. https://doi.org/10.1007/s00253-011-3743-z	-
Oceanimonas doudoroffii	JCM21046T	Numata, K., & Morisaki, K. (2015). Screening of Marine Bacteria To Synthesize Polyhydroxyalkanoate from Lignin: Contribution of Lignin Derivatives to Biosynthesis by Oceanimonas doudoroffii. ACS Sustainable Chemistry &amp; Engineering, 3(4), 569–573. https://doi.org/10.1021/acssuschemeng.5b00031	-
Pseudomonas putida	KT2440	Salvachúa, D., Karp, E. M., Nimlos, C. T., Vardon, D. R., & Beckham, G. T. (2015). Towards lignin consolidated bioprocessing: simultaneous lignin depolymerization and product generation by bacteria. Green Chemistry, 17(11), 4951–4967. https://doi.org/10.1039/c5gc01165e; Ravi, K., García-Hidalgo, J., Gorwa-Grauslund, M. F., & Lidén, G. (2017). Conversion of lignin model compounds by Pseudomonas putida KT2440 and isolates from compost. Applied Microbiology and Biotechnology, 101(12), 5059–5070. https://doi.org/10.1007/s00253-017-8211-y	-
Cupriavidus necator	JMP134	Salvachúa, D., Karp, E. M., Nimlos, C. T., Vardon, D. R., & Beckham, G. T. (2015). Towards lignin consolidated bioprocessing: simultaneous lignin depolymerization and product generation by bacteria. Green Chemistry, 17(11), 4951–4967. https://doi.org/10.1039/c5gc01165e; Pérez-Pantoja, D., De la Iglesia, R., Pieper, D. H., & González, B. (2008). Metabolic reconstruction of aromatic compounds degradation from the genome of the amazing pollutant-degrading bacteriumCupriavidus necatorJMP134. FEMS Microbiology Reviews, 32(5), 736–794. https://doi.org/10.1111/j.1574-6976.2008.00122.x	-
Rhodococcus jostii	RHA1	Salvachúa, D., Karp, E. M., Nimlos, C. T., Vardon, D. R., & Beckham, G. T. (2015). Towards lignin consolidated bioprocessing: simultaneous lignin depolymerization and product generation by bacteria. Green Chemistry, 17(11), 4951–4967. https://doi.org/10.1039/c5gc01165e	-
Candida parapsilosis	CBS604	Middelhoven, W. J., Coenen, A., Kraakman, B., & Sollewijn Gelpke, M. D. (1992). Degradation of some phenols and hydroxybenzoates by the imperfect ascomycetous yeastsCandida parapsilosis andArxula adeninivorans: evidence for an operative gentisate pathway. Antonie van Leeuwenhoek, 62(3), 181–187. https://doi.org/10.1007/bf00582578; Gérecová, G., Neboháčová, M., Zeman, I., Pryszcz, L. P., Tomáška, U., Gabaldón, T., & Nosek, J. (2015). Metabolic gene clusters encoding the enzymes of two branches of the 3-oxoadipate pathway in the pathogenic yeast Candida albicans. FEMS Yeast Research, 15(3). https://doi.org/10.1093/femsyr/fov006	-
Trichosporon cutaneum	CBS2466	Middelhoven, W. J. (1993). Catabolism of benzene compounds by ascomycetous and basidiomycetous yeasts and yeastlike fungi: A literature review and an experimental approach. Antonie van Leeuwenhoek, 63(2), 125–144. https://doi.org/10.1007/bf00872388	-
Rhodococcus fascians	AY730713	Song, Y. J. (2009). Characterization of aromatic hydrocarbon degrading bacteria isolated from pine litter.. Korean Journal of Microbiology and Biotechnology, 37, 333-339.	-
Pandoraea norimbergensis	LD001	Bandounas, L., Wierckx, N. J., de Winde, J. H., & Ruijssenaars, H. J. (2011). Isolation and characterization of novel bacterial strains exhibiting ligninolytic potential. BMC Biotechnology, 11(1). https://doi.org/10.1186/1472-6750-11-94	-
Agrobacterium tumefaciens	B6	Parke, D. (1997). Acquisition, reorganization, and merger of genes: novel management of the β-ketoadipate pathway in Agrobacterium tumefaciens. FEMS Microbiology Letters, 146(1), 3–12. https://doi.org/10.1016/s0378-1097(96)00382-5	-
Fusarium oxysporum	4287	Michielse, C. B., Reijnen, L., Olivain, C., Alabouvette, C., & Rep, M. (2012). Degradation of aromatic compounds through the β‐ketoadipate pathway is required for pathogenicity of the tomato wilt pathogen <scp>F</scp> usarium oxysporum f. sp. lycopersici. Molecular Plant Pathology, 13(9), 1089–1100. https://doi.org/10.1111/j.1364-3703.2012.00818.x	-
Rhodotorula mucilaginosa	CBS17	Sampaio, J. P. (1999). Utilization of low molecular weight aromatic compounds by heterobasidiomycetous yeasts: taxonomic implications. Canadian Journal of Microbiology, 45(6), 491–512. https://doi.org/10.1139/w99-020	-
Pseudomonas fluorescens	AN103	Paulsen, I. T., Press, C. M., Ravel, J., Kobayashi, D. Y., Myers, G. S. A., Mavrodi, D. V., DeBoy, R. T., Seshadri, R., Ren, Q., Madupu, R., Dodson, R. J., Durkin, A. S., Brinkac, L. M., Daugherty, S. C., Sullivan, S. A., Rosovitz, M. J., Gwinn, M. L., Zhou, L., Schneider, D. J., ... Loper, J. E. (2005). Complete genome sequence of the plant commensal Pseudomonas fluorescens Pf-5. Nature Biotechnology, 23(7), 873–878. https://doi.org/10.1038/nbt1110	-
Bacillus subtilis	KD8	Kuhnigk, T., & König, H. (1997). Degradation of dimeric lignin model compounds by aerobic bacteria isolated from the hindgut of xylophagous termites. Journal of Basic Microbiology, 37(3), 205–211. https://doi.org/10.1002/jobm.3620370309	-
Pseudomonas aeruginosa	KMD3	Kuhnigk, T., & König, H. (1997). Degradation of dimeric lignin model compounds by aerobic bacteria isolated from the hindgut of xylophagous termites. Journal of Basic Microbiology, 37(3), 205–211. https://doi.org/10.1002/jobm.3620370309	-
Bacillus licheniformis	KB1	Kuhnigk, T., & König, H. (1997). Degradation of dimeric lignin model compounds by aerobic bacteria isolated from the hindgut of xylophagous termites. Journal of Basic Microbiology, 37(3), 205–211. https://doi.org/10.1002/jobm.3620370309	-
Serratia marcescens	C5	Rhoads, T. L., Mikell Jr., A. T., & Eley, M. H. (1995). Investigation of the lignin-degrading activity of Serratia marcescens: biochemical screening and ultrastructural evidence. Canadian Journal of Microbiology, 41(7), 592–600. https://doi.org/10.1139/m95-079	-
Leucosporidium scottii	G43	Middelhoven, W. J. (1993). Catabolism of benzene compounds by ascomycetous and basidiomycetous yeasts and yeastlike fungi: A literature review and an experimental approach. Antonie van Leeuwenhoek, 63(2), 125–144. https://doi.org/10.1007/bf00872388	-
Exophiala jeanselmei	CBS 658.76	Middelhoven, W. J. (1993). Catabolism of benzene compounds by ascomycetous and basidiomycetous yeasts and yeastlike fungi: A literature review and an experimental approach. Antonie van Leeuwenhoek, 63(2), 125–144. https://doi.org/10.1007/bf00872388	-
Enterobacter aerogenes	L7	Deschamps, A. M., Mahoudeau, G., & Lebeault, J. M. (1980). Fast degradation of kraft lignin by bacteria. European Journal of Applied Microbiology and Biotechnology, 9(1), 45–51. https://doi.org/10.1007/bf00500001	-
Aeromonas sp.	L17	Deschamps, A. M., Mahoudeau, G., & Lebeault, J. M. (1980). Fast degradation of kraft lignin by bacteria. European Journal of Applied Microbiology and Biotechnology, 9(1), 45–51. https://doi.org/10.1007/bf00500001	-
Paenibacillus sp.	JJ-1b	Crawford, R. L., Bromley, J. W., & Perkins-Olson, P. E. (1979). Catabolism of protocatechuate by Bacillus macerans. Applied and Environmental Microbiology, 37(3), 614–618. https://doi.org/10.1128/aem.37.3.614-618.1979	-
Pseudomonas sp.	Isolate 9.1	Ravi, K., García-Hidalgo, J., Nöbel, M., Gorwa-Grauslund, M. F., & Lidén, G. (2018). Biological conversion of aromatic monolignol compounds by a Pseudomonas isolate from sediments of the Baltic Sea. AMB Express, 8(1). https://doi.org/10.1186/s13568-018-0563-x	-
Candida orthopsilosis	MCO457	Gérecová, G., Neboháčová, M., Zeman, I., Pryszcz, L. P., Tomáška, U., Gabaldón, T., & Nosek, J. (2015). Metabolic gene clusters encoding the enzymes of two branches of the 3-oxoadipate pathway in the pathogenic yeast Candida albicans. FEMS Yeast Research, 15(3). https://doi.org/10.1093/femsyr/fov006	-
Trichosporon oleaginosus	ATCC 20509	Yaguchi, A., Robinson, A., Mihealsick, E., & Blenner, M. (2017). Metabolism of aromatics by Trichosporon oleaginosus while remaining oleaginous. Microbial Cell Factories, 16(1). https://doi.org/10.1186/s12934-017-0820-8	-
Rhodosporidium toruloides	IFO0880	Yaegashi, J., Kirby, J., Ito, M., Sun, J., Dutta, T., Mirsiaghi, M., Sundstrom, E. R., Rodriguez, A., Baidoo, E., Tanjore, D., Pray, T., Sale, K., Singh, S., Keasling, J. D., Simmons, B. A., Singer, S. W., Magnuson, J. K., Arkin, A. P., Skerker, J. M., & Gladden, J. M. (2017). Rhodosporidium toruloides: a new platform organism for conversion of lignocellulose into terpene biofuels and bioproducts. Biotechnology for Biofuels, 10(1). https://doi.org/10.1186/s13068-017-0927-5	-
Marinobacterium georgiense	KW-40	GONZaLEZ, J. M., MAYER, F., MORAN, M. A., HODSON, R. E., & WHITMAN, W. B. (1997). Microbulbifer hydrolyticus gen. nov., sp. nov., and Marinobacterium georgiense gen. nov., sp. nov., Two Marine Bacteria from a Lignin-Rich Pulp Mill Waste Enrichment Community. International Journal of Systematic Bacteriology, 47(2), 369–376. https://doi.org/10.1099/00207713-47-2-369	-
Pseudomonas putida	Perestelo isolate 3	Perestelo, F., Rodríguez, A., Pérez, R., Carnicero, A., de la Fuente, G., & Falcón, M. A. (1996). Short communication: Isolation of a bacterium capable of limited degradation of industrial and labelled, natural and synthetic lignins. World Journal of Microbiology and Biotechnology, 12(1), 111–112. https://doi.org/10.1007/bf00327817	-
Acinetobacter calcoaceticus	DSM 586	Delneri, D., Degrassi, G., Rizzo, R., & Bruschi, C. V. (1995). Degradation of trans-ferulic and p-coumaric acid byAcinetobacter calcoaceticus DSM 586. Biochimica et Biophysica Acta (BBA) - General Subjects, 1244(2–3), 363–367. https://doi.org/10.1016/0304-4165(95)00021-3	-
Sphingobium sp.	SYK-6	Katayama, Y., Nishikawa, S., Murayama, A., Yamasaki, M., Morohoshi, N., & Haraguchi, T. (1988). The metabolism of biphenyl structures in lignin by the soil bacterium (Pseudomonas paucimobilis SYK‐6). FEBS Letters, 233(1), 129–133. https://doi.org/10.1016/0014-5793(88)81369-3	-
Comamonas testosteroni	CNB-1	Ni, B., Zhang, Y., Chen, D. W., Wang, B. J., & Liu, S. J. (2012). Assimilation of aromatic compounds by Comamonas testosteroni: characterization and spreadability of protocatechuate 4,5-cleavage pathway in bacteria. Applied Microbiology and Biotechnology, 97(13), 6031–6041. https://doi.org/10.1007/s00253-012-4402-8	-
Pseudomonas putida	PRS2000	Ornston, L. N., & Parke, D. (1976). Properties of an inducible uptake system for beta-ketoadipate in Pseudomonas putida. Journal of Bacteriology, 125(2), 475–488. https://doi.org/10.1128/jb.125.2.475-488.1976	-
Rhodococcus erythropolis	TA421	Chung, S. Y., Maeda, M., Song, E., Horikoshij, K., & Kudo, T. (1994). A Gram-positive Polychlorinated Biphenyl-degrading Bacterium,Rhodococcus erythropolisStrain TA421, Isolated from a Termite Ecosystem. Bioscience, Biotechnology, and Biochemistry, 58(11), 2111–2113. https://doi.org/10.1271/bbb.58.2111	-
Alcaligenes faecalis	KD10	Kuhnigk, T., & König, H. (1997). Degradation of dimeric lignin model compounds by aerobic bacteria isolated from the hindgut of xylophagous termites. Journal of Basic Microbiology, 37(3), 205–211. https://doi.org/10.1002/jobm.3620370309	-
Acinetobacter baumannii	KMB1	Kuhnigk, T., & König, H. (1997). Degradation of dimeric lignin model compounds by aerobic bacteria isolated from the hindgut of xylophagous termites. Journal of Basic Microbiology, 37(3), 205–211. https://doi.org/10.1002/jobm.3620370309	-
Bacillus cereus	KD4	Kuhnigk, T., & König, H. (1997). Degradation of dimeric lignin model compounds by aerobic bacteria isolated from the hindgut of xylophagous termites. Journal of Basic Microbiology, 37(3), 205–211. https://doi.org/10.1002/jobm.3620370309	-
Comamonas acidovorans	KNB3	Kuhnigk, T., & König, H. (1997). Degradation of dimeric lignin model compounds by aerobic bacteria isolated from the hindgut of xylophagous termites. Journal of Basic Microbiology, 37(3), 205–211. https://doi.org/10.1002/jobm.3620370309	-
Pseudomonas citronellolis	KMA4	Kuhnigk, T., & König, H. (1997). Degradation of dimeric lignin model compounds by aerobic bacteria isolated from the hindgut of xylophagous termites. Journal of Basic Microbiology, 37(3), 205–211. https://doi.org/10.1002/jobm.3620370309	-
Bacillus sphaericus	KD7	Kuhnigk, T., & König, H. (1997). Degradation of dimeric lignin model compounds by aerobic bacteria isolated from the hindgut of xylophagous termites. Journal of Basic Microbiology, 37(3), 205–211. https://doi.org/10.1002/jobm.3620370309	-
Burkholderia cepacia	KF12	Kuhnigk, T., & König, H. (1997). Degradation of dimeric lignin model compounds by aerobic bacteria isolated from the hindgut of xylophagous termites. Journal of Basic Microbiology, 37(3), 205–211. https://doi.org/10.1002/jobm.3620370309	-
Streptomyces sp.	ZC2	Kuhnigk, T., & König, H. (1997). Degradation of dimeric lignin model compounds by aerobic bacteria isolated from the hindgut of xylophagous termites. Journal of Basic Microbiology, 37(3), 205–211. https://doi.org/10.1002/jobm.3620370309	-
Streptomyces coelicolor	A3(2) M600	Davis, J. R., & Sello, J. K. (2009). Regulation of genes in Streptomyces bacteria required for catabolism of lignin-derived aromatic compounds. Applied Microbiology and Biotechnology, 86(3), 921–929. https://doi.org/10.1007/s00253-009-2358-0	-
Rhodococcus opacus	PD630 (DSMZ 44193)	Henson, W. R., Campbell, T., DeLorenzo, D. M., Gao, Y., Berla, B., Kim, S. J., Foston, M., Moon, T. S., & Dantas, G. (2018). Multi-omic elucidation of aromatic catabolism in adaptively evolved Rhodococcus opacus. Metabolic Engineering, 49, 69–83. https://doi.org/10.1016/j.ymben.2018.06.009	-
Pseudomonas fluorescens	DSM 50090	Ravi, K., Abdelaziz, O. Y., Nöbel, M., García-Hidalgo, J., Gorwa-Grauslund, M. F., Hulteberg, C. P., & Lidén, G. (2018). RETRACTED ARTICLE: Bacterial conversion of depolymerized Kraft lignin. Biotechnology for Biofuels, 11(1). https://doi.org/10.1186/s13068-018-1240-7	-
Rhodococcus rhodochrous	116	Karlson, U., Dwyer, D. F., Hooper, S. W., Moore, E. R., Timmis, K. N., & Eltis, L. D. (1993). Two independently regulated cytochromes P-450 in a Rhodococcus rhodochrous strain that degrades 2-ethoxyphenol and 4-methoxybenzoate. Journal of Bacteriology, 175(5), 1467–1474. https://doi.org/10.1128/jb.175.5.1467-1474.1993; Karlson, U., Dwyer, D. F., Hooper, S. W., Moore, E. R., Timmis, K. N., & Eltis, L. D. (1993). Two independently regulated cytochromes P-450 in a Rhodococcus rhodochrous strain that degrades 2-ethoxyphenol and 4-methoxybenzoate. Journal of Bacteriology, 175(5), 1467–1474. https://doi.org/10.1128/jb.175.5.1467-1474.1993	-
Azoarcus anaerobius	LuFRes1	Gorny, N., Wahl, G., Brune, A., & Schink, B. (1992). A strictly anaerobic nitrate-reducing bacterium growing with resorcinol and other aromatic compounds. Archives of Microbiology, 158(1), 48–53. https://doi.org/10.1007/bf00249065	(anaerobically)
Desulfobacterium catecholicum	NZva20	Szewzyk, R., & Pfennig, N. (1987). Complete oxidation of catechol by the strictly anaerobic sulfate-reducing Desulfobacterium catecholicum sp. nov.. Archives of Microbiology, 147(2), 163–168. https://doi.org/10.1007/bf00415278	(anaerobically)
Thauera aromatica	K172	Tschech, A., & Fuchs, G. (1987). Anaerobic degradation of phenol by pure cultures of newly isolated denitrifying pseudomonads. Archives of Microbiology, 148(3), 213–217. https://doi.org/10.1007/bf00414814; Tschech, A., & Fuchs, G. (1987). Anaerobic degradation of phenol by pure cultures of newly isolated denitrifying pseudomonads. Archives of Microbiology, 148(3), 213–217. https://doi.org/10.1007/bf00414814	(anaerobically); (anaerobically)
Burkholderia cepacia	Song isolate 1	Song, Y. J. (2009). Characterization of aromatic hydrocarbon degrading bacteria isolated from pine litter.. Korean Journal of Microbiology and Biotechnology, 37, 333-339.	-
Pantoea dispersa	Song isolate 2	Song, Y. J. (2009). Characterization of aromatic hydrocarbon degrading bacteria isolated from pine litter.. Korean Journal of Microbiology and Biotechnology, 37, 333-339.	-
Rhodococcus fascians	Song isolate 3	Song, Y. J. (2009). Characterization of aromatic hydrocarbon degrading bacteria isolated from pine litter.. Korean Journal of Microbiology and Biotechnology, 37, 333-339.	-
Flavimonas oryzihabitans	Song isolate 4	Song, Y. J. (2009). Characterization of aromatic hydrocarbon degrading bacteria isolated from pine litter.. Korean Journal of Microbiology and Biotechnology, 37, 333-339.	-
Microbacterium esteraromaticum	Song isolate 5	Song, Y. J. (2009). Characterization of aromatic hydrocarbon degrading bacteria isolated from pine litter.. Korean Journal of Microbiology and Biotechnology, 37, 333-339.	-
Acetobacterium woodii	NZva16	Bache, R., & Pfennig, N. (1981). Selective isolation of Acetobacterium woodii on methoxylated aromatic acids and determination of growth yields. Archives of Microbiology, 130(3), 255–261. https://doi.org/10.1007/bf00459530	(anaerobically)
Thauera sp.	Cin3,4	Mechichi, T., Patel, B. K., & Sayadi, S. (2005). Anaerobic degradation of methoxylated aromatic compounds by Clostridium methoxybenzovorans and a nitrate-reducing bacterium Thauera sp. strain Cin3,4. International Biodeterioration &amp; Biodegradation, 56(4), 224–230. https://doi.org/10.1016/j.ibiod.2005.09.001	-
Rhodopseudomonas palustris	CGA001	Harwood, C. S., & Gibson, J. (1988). Anaerobic and aerobic metabolism of diverse aromatic compounds by the photosynthetic bacterium Rhodopseudomonas palustris. Applied and Environmental Microbiology, 54(3), 712–717. https://doi.org/10.1128/aem.54.3.712-717.1988	-
Cupriavidus pinatubonensis	1245	Sato, Y., Nishihara, H., Yoshida, M., Watanabe, M., Rondal, J. D., Concepcion, R. N., & Ohta, H. (2006). Cupriavidus pinatubonensis sp. nov. and Cupriavidus laharis sp. nov., novel hydrogen-oxidizing, facultatively chemolithotrophic bacteria isolated from volcanic mudflow deposits from Mt. Pinatubo in the Philippines. International Journal of Systematic and Evolutionary Microbiology, 56(5), 973–978. https://doi.org/10.1099/ijs.0.63922-0	-
Amycolatopsis sp.	75iv2 (ATCC 39116)	Pometto III, A. L., Sutherland, J. B., & Crawford, D. L. (1981). Streptomyces setonii: catabolism of vanillic acid via guaiacol and catechol. Canadian Journal of Microbiology, 27(6), 636–638. https://doi.org/10.1139/m81-097; Sutherland, J. B., Crawford, D. L., & Pometto III, A. L. (1983). Metabolism of cinnamic, p-coumaric, and ferulic acids by Streptomyces setonii. Canadian Journal of Microbiology, 29(10), 1253–1257. https://doi.org/10.1139/m83-195	-
Haloarcula sp.	D1	Fairley, D. J., Boyd, D. R., Sharma, N. D., Allen, C. C. R., Morgan, P., & Larkin, M. J. (2002). Aerobic Metabolism of 4-Hydroxybenzoic Acid in Archaea via an Unusual Pathway Involving an Intramolecular Migration (NIH Shift). Applied and Environmental Microbiology, 68(12), 6246–6255. https://doi.org/10.1128/aem.68.12.6246-6255.2002	-
Haloferax sp.	C-24	Erdoğmuş, S. F., Mutlu, B., Korcan, S. E., Güven, K., & Konuk, M. (2013). Aromatic Hydrocarbon Degradation by Halophilic Archaea Isolated from Çamaltı Saltern, Turkey. Water, Air, &amp; Soil Pollution, 224(3). https://doi.org/10.1007/s11270-013-1449-9	-
Halorubrum ezzemoulense	C-46	Erdoğmuş, S. F., Mutlu, B., Korcan, S. E., Güven, K., & Konuk, M. (2013). Aromatic Hydrocarbon Degradation by Halophilic Archaea Isolated from Çamaltı Saltern, Turkey. Water, Air, &amp; Soil Pollution, 224(3). https://doi.org/10.1007/s11270-013-1449-9	-
Desulfobacterium phenolicum	Ph01	Bak, F., & Widdel, F. (1986). Anaerobic degradation of phenol and phenol derivatives by Desulfobacterium phenolicum sp. nov.. Archives of Microbiology, 146(2), 177–180. https://doi.org/10.1007/bf00402347; Bak, F., & Widdel, F. (1986). Anaerobic degradation of phenol and phenol derivatives by Desulfobacterium phenolicum sp. nov.. Archives of Microbiology, 146(2), 177–180. https://doi.org/10.1007/bf00402347	(anaerobically); (anaerobically)
Comamonas testosteroni	BR6020	Providenti, M. A., Mampel, J., MacSween, S., Cook, A. M., & Wyndham, R. C. (2001). Comamonas testosteroni BR6020 possesses a single genetic locus for extradiol cleavage of protocatechuate The GenBank accession number for the sequence reported in this paper is AF305325.. Microbiology, 147(8), 2157–2167. https://doi.org/10.1099/00221287-147-8-2157	-
Sulfuritalea hydrogenivorans	sk43H	Sperfeld, M., Diekert, G., & Studenik, S. (2018). Anaerobic aromatic compound degradation in Sulfuritalea hydrogenivorans sk43H. FEMS Microbiology Ecology. https://doi.org/10.1093/femsec/fiy199	(anaerobically)
Rhodosporidiobolus colostri	DBVPG 10655	Margesin, R., Ludwikowski, T. M., Kutzner, A., & Wagner, A. O. (2022). Low-Temperature Biodegradation of Lignin-Derived Aromatic Model Monomers by the Cold-Adapted Yeast Rhodosporidiobolus colostri Isolated from Alpine Forest Soil. Microorganisms, 10(3), 515. https://doi.org/10.3390/microorganisms10030515	-
Paraburkholderia aromaticivorans	AR20-38	Margesin, R., Volgger, G., Wagner, A. O., Zhang, D., & Poyntner, C. (2021). Biodegradation of lignin monomers and bioconversion of ferulic acid to vanillic acid by Paraburkholderia aromaticivorans AR20-38 isolated from Alpine forest soil. Applied Microbiology and Biotechnology, 105(7), 2967–2977. https://doi.org/10.1007/s00253-021-11215-z	-
Sphingomonas aromaticivorans	F199	Cecil, J. H., Garcia, D. C., Giannone, R. J., & Michener, J. K. (2018). Rapid, Parallel Identification of Catabolism Pathways of Lignin-Derived Aromatic Compounds in Novosphingobium aromaticivorans. Applied and Environmental Microbiology, 84(22). https://doi.org/10.1128/aem.01185-18	-
