@article {3289,
	title = {ARSENIC BIOMETHYLATION BY THE MICROORGANISM APIOTRICHUM HUMICOLA IN THE PRESENCE OF L-METHIONINE-METHYL-D(3)},
	journal = {Applied Organometallic Chemistry},
	volume = {9},
	number = {7},
	year = {1995},
	note = {ISI Document Delivery No.: TG189Times Cited: 15Cited Reference Count: 273rd International Conference on Environmental and Biological Aspects of Main Group Organometals (ICEBAMO 94)SEP, 1994BORDEAUX, FRANCESoc Francaise Chim, Royal Soc Chem, CNRS, EC Measurement \& Testing Program, French Minist Environm, French Minist Res \& Technol, Univ Bordeaux I, Univ Bordeaux II, IFREMER, INRA, Conseil Reg Aquitaine, Lyonnaise Eaux Dumez Water Co., Thermo Jarell Ash, John Wiley \& Sons, Freund Publ, Elsevier Sci Publ},
	month = {Nov},
	pages = {507-515},
	type = {Proceedings Paper},
	abstract = {The microorganism Apiotrichum humicola (previously known as Candida humicola) grown in the presence of either arsenate, arsenite, methyl-arsonic acid or dimethylarsinic acid, produces arsenic-containing metabolites in the growth medium. When L-methionine-methyl-d(3) is added to the cultures, the CD3 label is incorporated intact into the metabolites to a considerable extent to form deuterated dimethylarsenic and trimethylarsenic species, indicating that S-adenosylmethionine, or some related sulphonium compound, is involved in the biological methylation. Conclusive evidence of CD3 incorporation in the arsenicals found in the growth medium was provided by using a specially developed hydride generation-gas chromatography-mass spectrometry system (HG-GC-MS).},
	keywords = {ARSENATE, ARSENITE, CHROMATOGRAPHY MASS SPECTROMETRY, DIMETHYLARSINIC ACID, EXTRACELLULAR, GAS, HYDRIDE GENERATION, HYDRIDE GENERATION GAS, L-METHIONINE-METHYL-D(3), methylarsonic acid, METHYLATION, MICROORGANISM, REDUCTION, S-ADENOSYLMETHIONINE, THIOLS, TRIMETHYLARSINE OXIDE},
	isbn = {0268-2605},
	url = {<Go to ISI>://A1995TG18900002},
	author = {Cullen, W. R. and Li, H. and Pergantis, S. A. and Eigendorf, G. K. and Mosi, A. A.}
}
@article {3002,
	title = {IDENTIFICATION OF EXTRACELLULAR ARSENICAL METABOLITES IN THE GROWTH-MEDIUM OF THE MICROORGANISMS APIOTRICHUM-HUMICOLA AND SCOPULARIOPSIS-BREVICAULIS},
	journal = {Applied Organometallic Chemistry},
	volume = {8},
	number = {4},
	year = {1994},
	note = {ISI Document Delivery No.: PD643Times Cited: 34Cited Reference Count: 28},
	month = {Jul},
	pages = {303-311},
	type = {Article},
	abstract = {The separation and identification of some of the arsenic species produced in cells present in the growth medium when the microorganisms Apiotrichum humicola (previously known as Candida humicola) and Scopulariopsis brevicaulis were grown in the presence of arsenicals were achieved by using hydride generation-gas chromatography-atomic absorption spectrometry methodology (HG GC AA). Arsenite, monomethylarsonate, dimethylarsinate and trimethylarsine oxide were detected following incubation with arsenate. With arsenite as a substrate, the metabolites were monomethylarsonate, dimethylarsinate and trimethylarsine oxide; monomethylarsonate afforded dimethylarsinate and trimethylarsine oxide, and dimethylarsinate afforded trimethylarsine oxide. Trimethylarsine was not detected when the arsenic concentration was 1 ppm.},
	keywords = {APIOTRICHUM-HUMICOLA, arsenic, CANDIDA-HUMICOLA, DIMETHYULARSINATE, ENDOCELLULAR, EXTRACELLULAR, GROWTH MEDIUM, HYDRIDE GENERATION GAS CHROMATOGRAPHY ATOMIC ABSORPTION SPECTROMETRY, METHYLARSONATE, METHYLATION, mobility, SCOPULARIOPSIS-BREVICAULIS, TRIMETHYLARSINE, TRIMETHYLARSINE OXIDE},
	isbn = {0268-2605},
	url = {<Go to ISI>://A1994PD64300003},
	author = {Cullen, W. R. and Li, H. and Hewitt, G. and Reimer, K. J. and Zalunardo, N.}
}
@article {7203,
	title = {IRON PORPHYRIN CATALYZED OXIDATION OF LIGNIN MODEL COMPOUNDS - THE OXIDATION OF VERATRYL ALCOHOL AND VERATRYL ACETATE},
	journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie},
	volume = {70},
	number = {8},
	year = {1992},
	note = {ISI Document Delivery No.: JW564Times Cited: 13Cited Reference Count: 43},
	month = {Aug},
	pages = {2314-2318},
	type = {Article},
	abstract = {meso-Tetra(2,6-dichloro-3-sulfonatophenyl)porphyrin iron chloride catalyzes the oxidation of 3,4-dimethoxybenzyl alcohol (veratryl alcohol) in aqueous solution to give veratraldehyde along with demethoxylation and ring-cleavage products. The isolation of a direct ring-cleavage product from the oxidation of veratryl acetate in aqueous solution supports the previously proposed ring-cleavage mechanisms. The oxidation in methanol, however, does not lead to ring-cleavage products. When veratryl alcohol was oxidized in methanol, solvent was found to be incorporated into the 3-position of veratryl alcohol, giving new insight into the mechanism of oxidation.},
	keywords = {3, 4-DIMETHOXYBENZYL ALCOHOL, BASIDIOMYCETE PHANEROCHAETE-CHRYSOSPORIUM, BOND-CLEAVAGE, C, CLEAVAGE, DEGRADING ENZYME, DIARYLPROPANE OXYGENASE, EXTRACELLULAR, HEME-ENZYME, LIGNINASES, RING, SPECTRAL CHARACTERIZATION, WHITE ROT BASIDIOMYCETE},
	isbn = {0008-4042},
	url = {<Go to ISI>://A1992JW56400025},
	author = {Cui, F. T. and Dolphin, D.}
}
