Anaerobic Degradation of Choline

THE COLORIMETRIC DETERMINATION OF PHOSPHORUS

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COENZYME A FUNCTION IN AND ACETYL TRANSFER BY THE PHOSPHOTRANSACETYLASE SYSTEM

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THE OXIDATION OF ACETALDEHYDE TO ACETYL COENZYME A

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Yeast aldehyde dehydrogenase

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ANAEROBIC DEGRADATION OF CHOLINE I. , Vibrio cholinicus n. sp

Hayward, H. R., & Stadtman, T. C. (1959) · Journal of Bacteriology · doi:10.1128/jb.78.4.557-561.1959 · Cited by 68 · see citing works

ALDEHYDE OXIDATION

Jakoby, W. B. (1958) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)70376-1 · Cited by 59 · see citing works

The Separation of Choline Esters by Paper Chromatography.

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Anaerobic Degradation of Choline

Hayward, H. R., & Stadtman, T. C. (1960) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)69563-8 · Cited by 34 · see citing works

Intestinal Microbiota Composition Modulates Choline Bioavailability from Diet and Accumulation of the Proatherogenic Metabolite Trimethylamine- <i>N</i> -Oxide

Romano, K. A., Vivas, E. I., Amador-Noguez, D., & Rey, F. E. (2015) · mBio · doi:10.1128/mbio.02481-14 · Cited by 777 · see citing works

Microbial conversion of choline to trimethylamine requires a glycyl radical enzyme

Craciun, S., & Balskus, E. P. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1215689109 · Cited by 701 · see citing works

Dissimilatory Sulfate- and Sulfur-Reducing Prokaryotes

Rabus, R., Hansen, T. A., & Widdel, F. (2013) · Springer eBooks · doi:10.1007/978-3-642-30141-4_70 · Cited by 444 · see citing works

A Post-Genomic View of the Ecophysiology, Catabolism and Biotechnological Relevance of Sulphate-Reducing Prokaryotes

Rabus, R., Venceslau, S. S., Wöhlbrand, L., Voordouw, G., Wall, J. D., & Pereira, I. A. C. (2015) · Advances in microbial physiology/Advances in Microbial Physiology · doi:10.1016/bs.ampbs.2015.05.002 · Cited by 355 · see citing works

Dissimilatory Sulfate- and Sulfur-Reducing Prokaryotes

Rabus, R., Hansen, T. A., & Widdel, F. (2006) · Springer eBooks · doi:10.1007/0-387-30742-7_22 · Cited by 265 · see citing works

Physiology and ecology of the sulphate‐reducing bacteria

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Osmotic control of glycine betaine biosynthesis and degradation in Rhizobium meliloti

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Characterization and Detection of a Widely Distributed Gene Cluster That Predicts Anaerobic Choline Utilization by Human Gut Bacteria

Martínez-del Campo, A., Bodea, S., Hamer, H. A., Marks, J. A., Haiser, H. J., Turnbaugh, P. J., & Balskus, E. P. (2015) · mBio · doi:10.1128/mbio.00042-15 · Cited by 224 · see citing works

Metabolism of sulfate-reducing prokaryotes

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Recent advances in the study of the sulfate-reducing bacteria

Postgate, J. R. (1965) · Bacteriological Reviews · doi:10.1128/br.29.4.425-441.1965 · Cited by 174 · see citing works

Conversion of Dietary Choline to Trimethylamine and Dimethylamine in Rats: Dose-Response Relationship

Zeisel, S. H., daCosta, K. A., Youssef, M., & Hensey, S. (1989) · The Journal of Nutrition · doi:10.1093/jn/119.5.800 · Cited by 151 · see citing works

The Clostridial Fermentations of Choline and Ethanolamine

Bradbeer, C. (1965) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)97007-9 · Cited by 116 · see citing works

The aerobic decomposition of choline by microorganisms

Kortstee, G. J. J. (1970) · Archives of Microbiology · doi:10.1007/bf00410157 · Cited by 81 · see citing works

Volatile constituents of dog (Canis familiaris) and coyote (Canis latrans) anal sacs

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Degradation of various amine compounds by mesophilic clostridia

M�ller, B., Hippe, H., & Gottschalk, G. (1986) · Archives of Microbiology · doi:10.1007/bf00413032 · Cited by 50 · see citing works

Mechanism of biosynthesis of trimethylamine oxide from choline in the teleost tilapia, Oreochromis niloticus, under freshwater conditions

Niizeki, N., Daikoku, T., Hirata, T., El-Shourbagy, I., Song, X., & Sakaguchi, M. (2002) · Comparative Biochemistry and Physiology Part B Biochemistry and Molecular Biology · doi:10.1016/s1096-4959(01)00508-5 · Cited by 38 · see citing works

Fixation of Dinitrogen by Free-Living Microorganisms

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Choline and N , N -Dimethylethanolamine as Direct Substrates for Methanogens

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Role of Acetaldehyde in Metabolism: A Review 1. Enzymes Catalyzing Reactions Involving Acetaldehyde

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Converging on a mechanism for choline degradation

Thibodeaux, C. J., & van der Donk, W. A. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1219534110 · Cited by 28 · see citing works

Significance of yeast peroxisomes in the metabolism of choline and ethanolamine

Zwart, K. B., Marten Veenhuis, A., & Harder, W. (1983) · Antonie van Leeuwenhoek · doi:10.1007/bf00399317 · Cited by 27 · see citing works

Formation of trimethylamine from dietary choline by streptococcus sanguis I, which colonizes the mouth

Chao, C.-K., & Zeisel, S. H. (1990) · The Journal of Nutritional Biochemistry · doi:10.1016/0955-2863(90)90055-p · Cited by 23 · see citing works

Aerobic degradation of choline by <i>Proteus mirabilis</i>: enzymatic requirements and pathway

Sandhu, S. S., & Chase Jr., T. (1986) · Canadian Journal of Microbiology · doi:10.1139/m86-135 · Cited by 18 · see citing works

Biotransformation of alkanoylcholines under methanogenic conditions

Watson, M. K., Tezel, U., & Pavlostathis, S. G. (2012) · Water Research · doi:10.1016/j.watres.2012.03.021 · Cited by 17 · see citing works

Mechanism of biosynthesis of trimethylamine oxide in tilapia reared under seawater conditions

Niizeki, N., Daikoku, T., Hirata, T., El-Shourbagy, I., Song, X., & Sakaguchi, M. (2003) · Fisheries Science · doi:10.1046/j.1444-2906.2003.00590.x · Cited by 15 · see citing works

Über die Abbaufähigkeit bestimmterPseudomonas-Species für (—)-Carnitin

Strack, E., Aurich, H., & Grüner, E. (1964) · Journal of Basic Microbiology · doi:10.1002/jobm.3630040208 · Cited by 12 · see citing works

15 B12 Coenzyme-Dependent Amino Group Migrations

Stadtman, T. C. (1972) · The Enzymes · doi:10.1016/s1874-6047(08)60050-5 · Cited by 11 · see citing works

Isolation and Characterization of a Pseudomonas putida Strain able to Grow with Trimethyl-1,2-dihydroxy-propyl-ammonium as Sole Source of Carbon, Energy and Nitrogen

Kaech, A., & Egli, T. W. (2001) · Systematic and Applied Microbiology · doi:10.1078/0723-2020-00043 · Cited by 10 · see citing works

Production of trimethylamine from structurally related trimethylammonium compounds by resting cell suspensions of ?-butyrobetaine- and D,l-carnitine-grown Acinetobacter calcoaceticus and Pseudomonas putida

Englard, S., Blanchard, J. S., & Miura-Fraboni, J. (1983) · Archives of Microbiology · doi:10.1007/bf00413486 · Cited by 10 · see citing works

Isolation and characterization of heterotrophic bacteria able to grow aerobically with quaternary ammonium alcohols as sole source of carbon and nitrogen

Kaech, A., Vallotton, N., & Egli, T. W. (2005) · Systematic and Applied Microbiology · doi:10.1016/j.syapm.2004.12.004 · Cited by 9 · see citing works

Über die Abbaufähigkeit bestimmter Pseudomonas‐Species für (—)‐Carnitin

Strack, E., Aurich, H., & Grüner, E. (1964) · Zeitschrift für allgemeine Mikrobiologie · doi:10.1002/jobm.19640040208 · Cited by 8 · see citing works

Infrared Spectra of some Sulphate-Reducing Bacteria

Booth, G. H., Miller, J. D., Paisley, H. M., & Saleh, A. M. (1966) · Journal of General Microbiology · doi:10.1099/00221287-44-1-83 · Cited by 8 · see citing works

A Piezoelectric Microelectrode Arrays System for Real-Time Monitoring of Bacterial Contamination in Fresh Milk

Ren, J., Zhou, Y., Zhou, Y., Zhou, C. Q., Li, Z., Lin, Q., & Huang, H. (2014) · Food and Bioprocess Technology · doi:10.1007/s11947-014-1394-7 · Cited by 7 · see citing works

Status of names of bacterial taxa not evaluated in Index Bergeyana (1966): 1. Names published circa 1950-1967 exclusive of the genus Salmonella

HATT, H. D., & ZVIRBULIS, E. (1967) · International Journal of Systematic Bacteriology · doi:10.1099/00207713-17-2-171 · Cited by 7 · see citing works

Potential effects of natural dietary compounds on trimethylamine N -oxide (TMAO) formation and TMAO-induced atherosclerosis

Chen, P., Ho, C., Shahidi, F., & Pan, M. (2018) · Journal of Food Bioactives · doi:10.31665/jfb.2018.3151 · Cited by 6 · see citing works

Osmoregulation in Rhizobium Meliloti: Control of Glycine Betaine Biosynthesis and Catabolism

Rudulier, D. L., & Pocard, J. (1991) · Springer eBooks · doi:10.1007/978-1-4615-3730-4_11 · Cited by 1 · see citing works

Recent Advances intheStudyoftheSulfate-Reducing Bacteria

Postgate, J. R. (1965)

Dissimilation of Ethanol and Related Compounds by Desulfovibrio Strains

Hansen, T. A., & Kremer, D. R. (1990) · Springer eBooks · doi:10.1007/978-1-4613-0613-9_16

Epigenetics and Modification of Gene Expression in Metabolism

Heber, D. (2023) · Elsevier eBooks · doi:10.1016/b978-0-443-15315-0.00009-2

Steric and Electronic Effects in the Enzymatic Catalysis of Choline-TMA Lyase

Gogonea, V., & Hazen, S. L. (2025) · Biomolecules · doi:10.3390/biom16010037

Biochemistry of the Anaerobic Degradation of Non-Methane Alkanes

(2012) · SpringerReference · doi:10.1007/springerreference_168062

Anaerobic degradation: catabolism of xylene under denitrifying conditions

Kuhn, E. P., & Zeyer, J. (1986) · Cellular and Molecular Life Sciences · doi:10.1007/bf01975952

Anaerobic Digestion of CHLOrphenolic Wastes

Arshad, A., Hashmi, H. N., & Qureashi, I. A. (2011) · International Journal of Environmental Research · doi:10.22059/ijer.2010.300 · Cited by 12 · see citing works

Anaerobic degradation of chlorinated solvents

Magar, V. S. (2001) · Battelle Press eBooks · Cited by 30 · see citing works

Anaerobic Degradation of Aromatic Hydrocarbons

(2012) · SpringerReference · doi:10.1007/springerreference_168063 · Cited by 10 · see citing works