ArticleProceedings of the National Academy of Sciences of the United States of America2015
Entner-Doudoroff pathway for sulfoquinovose degradation in Pseudomonas putida SQ1.
Article in Proceedings of the National Academy of Sciences of the United States of America, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.
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46 citing papers in PubMed, 81 citations in OpenAlex.
- Structural and mechanistic basis of sulfolytic C-S bond cleavage by an Fe(ii)/α-ketoglutarate-dependent sulfoquinovose dioxygenase.Chemical science · 2026Article
- The return of metabolism: biochemistry and physiology of glycolysis.Biological reviews of the Cambridge Philosophical Society · 2026Review
- Sulfoquinovose degradation by cow rumen microbiota.The ISME journal · 2026Article
- Widespread marine and freshwater distributions of active sulfoquinovose-degrading bacteria.The ISME journal · 2026Article
- Bacterial sulfoquinovose cycling across aquatic ecosystems.FEMS microbiology reviews · 2026Review
- Advances in microbial sulfoquinovose catabolism.Frontiers in microbiology · 2026Review
- Sulfoquinovose Catabolism inInternational journal of molecular sciences · 2025Article
- Article
- Sulfoquinovose is exclusively metabolized by the gut microbiota and degraded differently in mice and humans.Microbiome · 2025Article
- Structure, kinetics, and mechanism of Pseudomonas putida sulfoquinovose dehydrogenase, the first enzyme in the sulfoglycolytic Entner-Doudoroff pathway.The Biochemical journal · 2025Article
- Study of sulfoglycolysis iniScience · 2024Article
- Enantioselective transformation of phytoplankton-derived dihydroxypropanesulfonate by marine bacteria.The ISME journal · 2024Article
- AnaerobicFrontiers in microbiology · 2024Article
- AMP-dependent phosphite dehydrogenase, a phosphorylating enzyme in dissimilatory phosphite oxidation.Proceedings of the National Academy of Sciences of the United States of America · 2023Article
- Molecular basis of sulfolactate synthesis by sulfolactaldehyde dehydrogenase fromChemical science · 2023Article
- Oxygenolytic sulfoquinovose degradation by an iron-dependent alkanesulfonate dioxygenase.iScience · 2023Article
- A Variant of the Sulfoglycolytic Transketolase Pathway for the Degradation of Sulfoquinovose into Sulfoacetate.Applied and environmental microbiology · 2023Article
- Sulfoquinovose is a widespread organosulfur substrate for Roseobacter clade bacteria in the ocean.The ISME journal · 2023Article
- Implications of hydrogen sulfide in colorectal cancer: Mechanistic insights and diagnostic and therapeutic strategies.Redox biology · 2023Review
- New mechanisms for bacterial degradation of sulfoquinovose.Bioscience reports · 2022Review
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4 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Sulfoquinovose (SQ; 6-deoxy-6-sulfoglucose) is the polar head group of the plant sulfolipid SQ-diacylglycerol, and SQ comprises a major proportion of the organosulfur in nature, where it is degraded by bacteria. A first degradation pathway for SQ has been demonstrated recently, a "sulfoglycolytic" pathway, in addition to the classical glycolytic (Embden-Meyerhof) pathway in Escherichia coli K-12; half of the carbon of SQ is abstracted as dihydroxyacetonephosphate (DHAP) and used for growth, whereas a C3-organosulfonate, 2,3-dihydroxypropane sulfonate (DHPS), is excreted. The environmental isolate Pseudomonas putida SQ1 is also able to use SQ for growth, and excretes a different C3-organosulfonate, 3-sulfolactate (SL). In this study, we revealed the catabolic pathway for SQ in P. putida SQ1 through differential proteomics and transcriptional analyses, by in vitro reconstitution of the complete pathway by five heterologously produced enzymes, and by identification of all four organosulfonate intermediates. The pathway follows a reaction sequence analogous to the Entner-Doudoroff pathway for glucose-6-phosphate: It involves an NAD(+)-dependent SQ dehydrogenase, 6-deoxy-6-sulfogluconolactone (SGL) lactonase, 6-deoxy-6-sulfogluconate (SG) dehydratase, and 2-keto-3,6-dideoxy-6-sulfogluconate (KDSG) aldolase. The aldolase reaction yields pyruvate, which supports growth of P. putida, and 3-sulfolactaldehyde (SLA), which is oxidized to SL by an NAD(P)(+)-dependent SLA dehydrogenase. All five enzymes are encoded in a single gene cluster that includes, for example, genes for transport and regulation. Homologous gene clusters were found in genomes of other P. putida strains, in other gamma-Proteobacteria, and in beta- and alpha-Proteobacteria, for example, in genomes of Enterobacteria, Vibrio, and Halomonas species, and in typical soil bacteria, such as Burkholderia, Herbaspirillum, and Rhizobium.
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