Entner-Doudoroff pathway in Synechocystis PCC 6803: Proposed regulatory roles and enzyme multifunctionalities
Status PubMed-not-MEDLINE Jazyk angličtina Země Švýcarsko Médium electronic-ecollection
Typ dokumentu časopisecké články
PubMed
36051759
PubMed Central
PMC9424857
DOI
10.3389/fmicb.2022.967545
Knihovny.cz E-zdroje
- Klíčová slova
- Entner-Doudoroff pathway, cyanobacteria, glycolysis, kinetic model, metabolic regulation,
- Publikační typ
- časopisecké články MeSH
The Entner-Doudoroff pathway (ED-P) was established in 2016 as the fourth glycolytic pathway in Synechocystis sp. PCC 6803. ED-P consists of two reactions, the first catalyzed by 6-phosphogluconate dehydratase (EDD), the second by keto3-deoxygluconate-6-phosphate aldolase/4-hydroxy-2-oxoglutarate aldolase (EDA). ED-P was previously concluded to be a widespread (∼92%) pathway among cyanobacteria, but current bioinformatic analysis estimated the occurrence of ED-P to be either scarce (∼1%) or uncommon (∼47%), depending if dihydroxy-acid dehydratase (ilvD) also functions as EDD (currently assumed). Thus, the biochemical characterization of ilvD is a task pending to resolve this uncertainty. Next, we have provided new insights into several single and double glycolytic mutants based on kinetic model of central carbon metabolism of Synechocystis. The model predicted that silencing 6-phosphogluconate dehydrogenase (gnd) could be coupled with ∼90% down-regulation of G6P-dehydrogenase, also limiting the metabolic flux via ED-P. Furthermore, our metabolic flux estimation implied that growth impairment linked to silenced EDA under mixotrophic conditions is not caused by diminished carbon flux via ED-P but rather by a missing mechanism related to the role of EDA in metabolism. We proposed two possible, mutually non-exclusive explanations: (i) Δeda leads to disrupted carbon catabolite repression, regulated by 2-keto3-deoxygluconate-6-phosphate (ED-P intermediate), and (ii) EDA catalyzes the interconversion between glyoxylate and 4-hydroxy-2-oxoglutarate + pyruvate in the proximity of TCA cycle, possibly effecting the levels of 2-oxoglutarate under Δeda. We have also proposed a new pathway from EDA toward proline, which could explain the proline accumulation under Δeda. In addition, the presented in silico method provides an alternative to 13C metabolic flux analysis for marginal metabolic pathways around/below the threshold of ultrasensitive LC-MS. Finally, our in silico analysis provided alternative explanations for the role of ED-P in Synechocystis while identifying some severe uncertainties.
Zobrazit více v PubMed
Asplund-Samuelsson J., Hudson E. P. (2021). Wide range of metabolic adaptations to the acquisition of the Calvin cycle revealed by comparison of microbial genomes. PubMed DOI PMC
Bachhar A., Jablonsky J. (2020). A new insight into role of phosphoketolase pathway in PubMed DOI PMC
Bren A., Park J. O., Towbin B. D., Dekel E., Rabinowitz J. D., Alon U. (2016). Glucose becomes one of the worst carbon sources for PubMed DOI PMC
Campilongo R., Fung R., Little R., Grenga L., Trampari E., Pepe S., et al. (2017). One ligand, two regulators and three binding sites: How KDPG controls primary carbon metabolism in PubMed DOI PMC
Chen X., Schreiber K., Appel J., Makowka A., Fähnrich B., Roettger M., et al. (2016). The Entner-Doudoroff pathway is an overlooked glycolytic route in cyanobacteria and plants. PubMed DOI PMC
Daddaoua A., Krell T., Ramos J.-L. (2009). Regulation of glucose metabolism in PubMed DOI PMC
Dang L., White D. W., Gross S., Bennett B. D., Bittinger M. A., Driggers E. M., et al. (2009). Cancer-associated IDH1 mutations produce 2-hydroxyglutarate. PubMed DOI PMC
Daniel J., Danchin A. (1986). 2-Ketoglutarate as a possible regulatory metabolite involved in cyclic AMP-dependent catabolite repression in PubMed DOI
Deutscher J. (2008). The mechanisms of carbon catabolite repression in bacteria. PubMed DOI
Doello S., Klotz A., Makowka A., Gutekunst K., Forchhammer K. (2018). A specific glycogen mobilization strategy enables rapid awakening of dormant cyanobacteria from chlorosis. PubMed DOI PMC
Doucette C. D., Schwab D. J., Wingreen N. S., Rabinowitz J. D. (2011). α-ketoglutarate coordinates carbon and nitrogen utilization PubMed DOI PMC
Engene N., Rottacker E. C., Kaštovský J., Byrum T., Choi H., Ellisman M. H., et al. (2012). PubMed DOI PMC
Figueiredo A. S., Kouril T., Esser D., Haferkamp P., Wieloch P., Schomburg D., et al. (2017). Systems biology of the modified branched Entner-Doudoroff pathway in PubMed DOI PMC
Flamholz A., Noor E., Bar-Even A., Liebermeister W., Milo R. (2013). Glycolytic strategy as a tradeoff between energy yield and protein cost. PubMed DOI PMC
Fuhrman L. K., Wanken A., Nickerson K. W., Conway T. (1998). Rapid accumulation of intracellular 2-keto-3-deoxy-6-phosphogluconate in an Entner-Doudoroff aldolase mutant results in bacteriostasis. PubMed DOI
Hing N. Y. K., Liang F., Lindblad P., Morgan J. A. (2019). Combining isotopically non-stationary metabolic flux analysis with proteomics to unravel the regulation of the Calvin-Benson-Bassham cycle in PubMed DOI
Jablonsky J., Papacek S., Hagemann M. (2016). Different strategies of metabolic regulation in cyanobacteria: From transcriptional to biochemical control. PubMed DOI PMC
Kim J., Yeom J., Jeon C. O., Park W. (2009). Intracellular 2-keto-3-deoxy-6-phosphogluconate is the signal for carbon catabolite repression of phenylacetic acid metabolism in PubMed DOI
Kim S., Lee S. B. (2006). Catalytic promiscuity in dihydroxy-acid dehydratase from the thermoacidophilic archaeon PubMed DOI
Kopp D., Bergquist P. L., Sunna A. (2020). Enzymology of alternative carbohydrate catabolic pathways. DOI
Leyval D., Uy D., Delaunay S., Goergen J. L., Engasser J. M. (2003). Characterisation of the enzyme activities involved in the valine biosynthetic pathway in a valine-producing strain of PubMed DOI
Linington R. G., Edwards D. J., Shuman C. F., McPhail K. L., Matainaho T., Gerwick W. H. (2008). Symplocamide A, a potent cytotoxin and chymotrypsin inhibitor from the marine cyanobacterium PubMed DOI PMC
Lucius S., Makowka A., Michl K., Gutekunst K., Hagemann M. (2021). The Entner-Doudoroff pathway contributes to glycogen breakdown during high to low CO PubMed DOI PMC
Makowka A., Nichelmann L., Schulze D., Spengler K., Wittmann C., Forchhammer K., et al. (2020). Glycolytic shunts replenish the Calvin–Benson–Bassham cycle as anaplerotic reactions in cyanobacteria. PubMed DOI
Nakajima T., Kajihata S., Yoshikawa K., Matsuda F., Furusawa C., Hirasawa T., et al. (2014). Integrated metabolic flux and omics analysis of PubMed DOI
Orthwein T., Scholl J., Spaet P., Lucius S., Koch M., Macek B., et al. (2021). The novel P-II-interactor PirC identifies phosphoglycerate mutase as key control point of carbon storage metabolism in cyanobacteria. PubMed DOI PMC
Pimentel J. S. M., Giani A. (2014). Microcystin production and regulation under nutrient stress conditions in toxic microcystis strains. PubMed DOI PMC
Richhardt J., Bringer S., Bott M. (2012). Mutational analysis of the pentose phosphate and Entner-Doudoroff pathways in PubMed DOI PMC
Schulze D., Kohlstedt M., Becker J., Cahoreau E., Peyriga L., Makowka A., et al. (2022). GC/MS-based 13C metabolic flux analysis resolves the parallel and cyclic photomixotrophic metabolism of PubMed DOI PMC
Will S. E., Henke P., Boedeker C., Huang S., Brinkmann H., Rohde M., et al. (2019). Day and night: Metabolic profiles and evolutionary relationships of six axenic non-marine cyanobacteria. PubMed DOI PMC
Xiong W., Cano M., Wang B., Douchi D., Yu J. (2017). The plasticity of cyanobacterial carbon metabolism. PubMed DOI
Xiong W., Lee T.-C., Rommelfanger S., Gjersing E., Cano M., Maness P.-C., et al. (2015). Phosphoketolase pathway contributes to carbon metabolism in cyanobacteria. PubMed DOI
Yoshikawa K., Hirasawa T., Ogawa K., Hidaka Y., Nakajima T., Furusawa C., et al. (2013). Integrated transcriptomic and metabolomic analysis of the central metabolism of PubMed DOI
Zhang P., MacTavish B. S., Yang G., Chen M., Roh J., Newsome K. R., et al. (2020). Cyanobacterial dihydroxy-acid dehydratases are a promising growth inhibition target. PubMed DOI PMC
A quantitative description of light-limited cyanobacterial growth using flux balance analysis