|Home | About | Journals | Submit | Contact Us | Français|
The evolutionary origins of the tricarboxylic acid cycle (TCA), or Krebs cycle, are so far unclear. Despite a few years ago, the existence of a simple non-enzymatic Krebs-cycle catalyst has been dismissed ‘as an appeal to magic’, citrate and other intermediates have meanwhile been discovered on a carbonaceous meteorite and do interconvert non-enzymatically. To identify the non-enzymatic Krebs cycle catalyst, we used combinatorial, quantitative high-throughput metabolomics to systematically screen iron and sulfate reaction milieus that orient on Archean sediment constituents. TCA cycle intermediates are found stable in water and in the presence of most iron and sulfate species, including simple iron-sulfate minerals. However, we report that TCA intermediates undergo 24 interconversion reactions in the presence of sulfate radicals that form from peroxydisulfate. The non-enzymatic reactions critically cover a topology as present in the Krebs cycle, the glyoxylate shunt and the succinic semialdehyde pathways. Assembled in a chemical network, the reactions achieve more than ninety percent carbon recovery. Our results show that a non-enzymatic precursor for the Krebs cycle is biologically sensible, efficient, and forms spontaneously in the presence of sulfate radicals.
The tricarboxylic acid cycle (TCA), or Krebs cycle, is a central metabolic pathway typically of oxidative function. This metabolic pathway provides precursors for the biosynthesis of amino acids, is central to fatty acid breakdown, cellular respiration, energy and redox metabolism1. The widespread occurrence of at least its oxidative part2,3 indicates that the origins of at least parts of the Krebs cycle are to be placed to a very early stage in evolution, perhaps its oxidative reactions date back to origin of life4–6. A frequently discussed hypothesis proposes the Krebs cycle obtained its structural topology by Darwinian selection principles that were enabled by the ‘RNA world’. A post-genetic origin implies that pathway topologies are subject to progressive change, implying that the modern Krebs cycle could differ substantially from its early precursors7. A post-genetic origin of metabolism struggles however to explain how multiple, structurally complex enzymes came into being initially; enzymes themselves are made-up from the metabolic products of the Krebs cycle. Second, a Darwinian origin of the metabolic network topology has difficulties to explain the high number of reactions that are recurring between kingdoms despite a lack of enzyme sequence conservation8. An alternative hypothesis hence proposes that at least the key metabolic reactions originated from an environmental chemistry. In this scenario, the inorganic catalysis determine the basic structure of metabolism9–12.
As enzymatic mechanisms of the Krebs cycle have limited resemblance to inorganic catalysis, a non-enzymatic origin was received skeptically by many5,13. For instance, Leslie Orgel, a leading scientist in shaping the RNA world hypothesis, dismissed the possibility that a simple inorganic catalyst that could replace a series set of TCA-like reactions as ‘an appeal to magic’5. However, despite the simple catalyst was indeed missing so far, others have argued that several Krebs-cycle metabolites form in organic-chemical reactions9,10. Meanwhile, the presence of a series TCA intermediates has been confirmed on a carbonaceous meteorite 14. Furthermore, citrate and other TCA intermediates undergo highly efficient reductive, interconversion reactions on semiconductor particles upon strong UV light exposure15. A non-enzymatic precursor to the Krebs cycle is hence catalytically possible. Moreover, also the existence of an unifying, simple catalyst has become plausible. Non-enzymatic reactions that replicate two other metabolic pathways, glycolysis the pentose phosphate pathway, are unified by their dependency on the same catalyst and co-substrate, ferrous iron16,17. As Fe(II) is abundant in typical Archean sediments18,19 implies that the general chemical environments, rather than niche conditions, could have been key to shape the structure of metabolic pathways.
We choose a systematic screening strategy and addressed in ~4,850 absolute quantitative experiments the reactivity of TCA intermediates in the presence of typical Archean sediment constituents as well as related iron and sulfur species. We find TCA intermediates unreactive in the presence of the majority of iron and sulfate combinations, including the simple FeS mineral ferrous sulfide. In the presence of the radical donor peroxydisulfate however, we detect 24 non-enzymatic interconversion reactions. These reactions resemble the isomerisation and oxidative reactions of the enzymatic Krebs cycle, the glyoxylate shunt and the succinic semialdehyde pathway, so that their topologies are critically covered. A chemical network assembled from these reactions achieves more than 90% carbon recovery, forming a plausible non-enzymatic template for the origin of the early Krebs cycle.
We optimized the throughput of a liquid chromatography-multiple reaction monitoring (LC-MRM) method to absolutely quantify TCA intermediates in the 6,100 samples eventually created in this study. We next assessed the reactivity of citrate, cis-aconitate, isocitrate, α-ketoglutarate, succinate, fumarate, malate and oxaloacetate upon heat exposure in water and - and in order to account for the low oxygen concentrations of the pre-metabolic world20 - in an artificial nitrogen atmosphere. TCA intermediates were stable and did not react spontaneously into other TCA intermediates or other products (Figure 1AB, Supplementary Figure 1). The only exception was oxaloacetate that decarboxylated forming pyruvate (Figure 1B, Supplementary Figure 2). The Krebs cycle hence contrasts to glycolysis and pentose phosphate pathways, of which intermediates spontaneously interconvert16,17. Non-enzymatic TCA-like reactivity is hence highly depending on enabling chemistry. Further, these experiments served as important controls as they confirm the absence of enzymatic contamination.
Transition metals are prebiotically abundant and remain frequent metabolic catalysts 21. We tested a transition metal mixture that reflects iron, cobalt, nickel and molybdenum concentrations of typical Archean sediments18,19,22 and found that isocitrate reacted to α-ketoglutarate, succinate and pyruvate, and α-ketoglutarate to succinate (Figure 1C, Supplementary Table 1). These reactions were dependent Fe(II) (Supplementary Figure 3, Supplementary Table 2), and hence likely dependent on the α-hydroxyl or α-keto moieties specifically present in isocitrate and α-ketoglutarate that form iron contact sites (Figure 1D)23. Furthermore, these reactions followed a clear pH-profile (Supplementary Figure 4), similar to Fe(II) mediated glycolysis-like reactions17.
The low number of reactions ruled out the transition metal catalysis is sufficient to enable a non-enzymatic Krebs cycle (Figure 1D). A major bottleneck where the conversions of citrate to isocitrate and succinate to fumarate, typically catalyzed by iron-sulfur cluster enzymes24. Iron/sulfur minerals such as pyrite could have acted as catalysts in a prebiotic metabolism4, but mineral surfaces chemistry has little resemblance to metabolic catalysis either. We tested ferrous sulfide as a simple mimetic of an iron sulfur mineral, but detected no TCA-like reactions (Supplementary Tables 3-4 and Supplementary Figures 5-6). We continued with a systematic screen, testing ten sulfur-containing compounds, seven iron sources, and five TCA substrates in all possible combinations (Figure 2A). Again, most reaction mixtures had no effect on TCA intermediates (Figure 2B). However, a comprehensive spectrum of reactivity was enabled upon adding peroxydisulfate (Figure 2B, Supplementary Table 3). In the single-timepoint screening format, we detected up to 13 TCA-metabolite forming reactions (Figure 2B, Supplementary Figures 5-6).
We noticed that when combined with iron sources, in particular ferrous sulfide, the reaction spectrum enabled by peroxydisulphate was substantially altered. Most reactions were accelerated, while some intermediates were no longer observed at the expense of additional TCA metabolites that were formed (Supplementary Table 1). We hence continued with a detailed and quantitative (kinetic) characterization of the reactions starting from citrate, cis-aconitate, isocitrate, α-ketoglutarate, succinate, succinic semialdehyde, fumarate, and malate in the presence of peroxydisulphate in combination with ferrous sulfide. In the quantitative time series analyses, we detected 24 reactions that interconvert a TCA metabolite into another TCA intermediate (Fig 3A). A network graph assembled from these reactions reveals a high coverage of the topologies of the TCA cycle (by resembling its oxidative and isomerisation reactions), the glyoxylate shunt and the succinic semialdehyde pathways (Figure 3B-C).
Considering that our conditions were optimized to obtain a maximum number of TCA-like reactions, but not yield, the TCA-like chemical network was found extraordinarily efficient. After 2 h, 91.9% of the carbon was recovered in TCA intermediates, of which 42.3% were newly formed TCA metabolites. Only 8.1% reacted into non-TCA metabolites (including carbon dioxide) (Figure 3C).
The 24 non-enzymatic reactions did occur at an average rate of 0.280 µmol per min starting from the 100 µM substrates in the presence of peroxydisulphate and ferrous sulfide, but solely at 0.0433 µmol per min in the absence of ferrous sulfide. The interconversion of succinic semialdehyde to succinate was the fastest, and the reaction of citrate to succinate was the slowest reaction (Fig 3A, Supplementary Figure 7). Also the two reactions enabled by Fe(II) (Figure 1), were substantially faster in the peroxydisulfate/ferrous sulfide milieu, and did occur at 33.0% or 34.7%, of the Fe(II) rate (Figure S7, Supplementary Table 1). Further, the intermediates that were exclusively detected in the presence of peroxydisulphate, are likely exclusive to the simple milieu as they react faster to the downstream product than they are formed once the iron sources are combined with peroxydisulfate (Fig 3A). Peroxydisulfate can act via a radical one-electron and a two-electron mechanism25 and possesses a high oxidative potential26,27 which results from the donation of sulfate radicals, increasingly formed upon activation by iron and iron-containing sediments including pyrite28, other trace metals29,30, as well as by photolysis and thermolysis31,32. Implying that the TCA-like reactions are dependent on the formation of these radicals, we assessed the effects of hydrogen peroxide (H2O2), that in the presence of Fe(II), provides hydroxyl radicals in the Fenton reaction. 10 out of the 24 reactions were enabled also by H2O2 (Figure 4A, Supplementary Table 5). The specificity was however 83% lower and the reactions 91.1% slower (Figure 4A). Next, we exploited the differential scavenging properties of 2-propanol and tert-butanol. While 2-propanol efficiently scavenges both, hydroxyl and sulfate radicals (k(OH•) = 1.9*109 M-1s-1, k(SO4−•) = 8.2*107 M-1s-1), tert-butanol inefficiently scavenges the sulfate radical (k(SO4−•) = 8.5*105 M-1s-1, compared to the hydroxyl radical (k(OH•)= 5.2*108 M-1s-1) (Figure 4B, left panel)33. tert-butanol did not prevent TCA-like reactions, but scavenging of sulfate radicals by 2-propanol abolished most reactivity (Figure 4B, C, Supplementary Table 5). Radical quenching had lower impact on some reactions, which could be explained by incomplete scavenging or by non-radicalic activity of peroxydisulfate and its product (Figure 4D). For the majority of reactions, the presence of sulfate radicals was however essential.
All living cells possess a metabolic network whose topological structure is conserved between kingdoms, also for pathways like glycolysis and its variants where the enzymes are not sequence conserved. Sometimes confused with another important question about whether life was of heterotrophic or autotrophic origin34, the origin of this metabolic network remains a largely unsolved problem35–37. An increasing number of experiments reveal that its core structural parts are resemblant of spontaneous chemical reactions and non-enzymatic catalysis16,21,38A theory that explains the metabolic origin by an environmental inorganic chemistry is indeed attractive, as it facilitates a stepwise scenario for origin of enzymes39,40. In the presence of a chemical network not all enzymes that form pathway need to come into being at the same time to achieve a functional unit41. Second, a chemical system can be improved stepwise starting from its single most limiting reaction.
Fe(II) dependent on-enzymatic reactions that resemble glycolysis and the pentose phosphate pathway16,17 reveal that metabolism-like reaction networks can form on the basis of a simple and prebiotically abundant catalyst. Seen from another perspective, chemical reactions that are driven by the most abundant Archean transition metal are part of the metabolic network. Several key questions remain however unanswered. First, there is currently no prebiotically plausible scenario that forms the glycolytic and PPP precursors such as glucose-6-phosphate or 6-phosphogluconate, respectively. Further, it remains that glycolytic and PPP-like reactions cannot serve to explain the origin of other pathways that depend on a different chemistry, like the Krebs cycle, that does not possess phosphorylated intermediates.
Attractive about the Krebs cycle is that the non-enzymatic formation of its intermediates has has repeatedly been described, including their presence in high concentrations on a carbonaceous meteorite13–15. In the systematic search for a plausible Krebs-cycle catalyst, we excluded chemical conditions that can not persist within the boundaries of a cell (in particular UV light, high pressure, temperatures above 100°C), avoided niche conditions and metals that play virtually no role in metabolism (i.e. titan, borate). Instead, we screened metals important for metabolism that are frequent Archean sediment components, use low-oxygen conditions, and compromise on a temperature (70°C) that enables to measure slow reactions, yet that is within the range of life.
While TCA cycle intermediates were highly stable, our HTP screen revealed a single hit. Peroxydisulfate enabled a series of TCA-like reactivity, and we find that this property was dependent on the formation of sulfate radicals. The non-enzymatic reactions obtained reflect the oxidative and isomerisation reactivity of the Krebs cycle, the glyoxylate shunt and the succinic semialdehyde pathways (Fig 2) and form a chemical reaction network was of extraordinary high yield of > 90%. Indeed in several reactions the formation of non-TCA metabolites was negligible (Fig 3C). In other words, TCA metabolites interconvert specifically into TCA intermediates under the elaborated conditions, but barely form any other of the many thermodynamically possible products. To put this into perspective, the yield of the non-enzymatic network exceeds substantially that of an in vitro glycolysis based on E. coli purified enzymes 42. An explanation for this high specificity is provided by the physical-chemical properties of the sulfate radical. Compared to hydroxyl radicals with a half-life time of only 10-9 sec in water, sulfate radicals are orders of magnitude more stable, and persist for several seconds43. Furthermore, the sulfate radical carries a negative charge at physiological pH, and thus is affected by a repulsive force between itself and the substrates charged carboxyl groups. These electrostatic interactions limit the approachable reactive positions of TCA intermediates. In addition, the spatial dimensions of sulfate radicals create a steric burden that decreases the number of possible contact sides. All these properties limit the number of contact sites and reaction products, that are found the intermediates of the Krebs cycle, at least its stable end products of multi-step reactions as observed in our set-up (Supplementary Table 6). The reactions observed include decarboxylations, oxidoreductase like redox reactions, and dehydrations, and for some a reaction topology like in the TCA cycle is obtained. For instance, succinate is formed from citrate, aconitate, isocitrate, and α-ketoglutarate. These reactions show a similar dependency on sulfate radicals and a comparable quenching behaviour, This implies that succinate is formed in a reaction sequence that starts with citrate forming cis-aconitate, which is then converted to isocitrate, α-ketoglutarate, succinic semialdehyde and finally succinate. In contrast, the formation of pyruvate from citrate appears independent from radical species, while other pyruvate forming reactions are quenched by the radical scavenger. Pyruvate is hence formed by more than one reaction.
The dependency of almost all reactions on sulfate radicals could be indicative about the prebiotic environment in which the Krebs cycle emerged. Despite the reactive radicals themselves are not be preserved over billions of years, there are indirect traces of an early sulfur redox chemistry. Microfossils in 3.4-billion-year-old rocks of Western Australia are some of the earliest traces of life on Earth, and are characterized by pyrite microfossils of biotic origin44. This difference to glycolysis and the PPP, that depend on Fe(II) but not on sulfur species16. This observation might add an aspect to the endosymbiont theory. While glycolysis and the PPP are typically cytoplasmic, in most eukaryotic species that contain mitochondria, these are both the host of the TCA cycle and are responsible for the assembly of iron-sulfate clusters 45.
How could a series of non-enzymatic reaction enable the evolution of the Krebs ‘cycle’, that does not only interconvert and oxidize metabolites, but is is also implicated in anabolism and that contains key co-factor coupled reactions? To complete the Krebs cycle, a C-C forming reaction to yield citrate as catalyzed by citrate synthase is required but missing. However a full or reductive cycle is present only in a subset of species, and hence unlikely the evolutionary starting point for the Krebs cycle2,3. Indeed, an oxidative directionality is the expected thermodynamic outcome for non-enzymatic reactions. Cofactor-dependent reactions reverse the directionality in living systems, and these are considered a speciality of enzymatic catalysis. The closure of the TCA cycle by adding a citrate synthase enzyme could r provide a significant advantage upon adding a single enzymatic step, and hence provide an interesting case for the evolution of an enzyme-catalysed metabolism. One possibility hence consists that first versions of the Krebs cycle could have been of heterotrophic nature that obtained precursors from environmental-chemical reactions that do not necessarily need to possess resemblances with metabolic pathways14,15. Alternatively, we would like to speculate that there is also no need for an early closure of the Krebs cycle, if its oxidative reactions are fed by other metabolism-like reactions, like a carboxylation of pyruvate enabled in a coupling to an early glycolysis. The existence of non-enzymatic pyruvate carboxylase reaction latter could unify key issues of explaining the origins of glycolysis, the PPP and the Krebs cycle.
In summary, we describe a mutually compatible, efficient, non-enzymatic catalysis that interconverts TCA cycle intermediates. The reactions are enabled by sulfate radicals that form upon the activation of peroxydisulfate. The chemical network coves the topology of the conserved (oxidative) part of the Krebs cycle, and achieves more than 90% carbon efficiency. The simplicity of the environment that is based on a unifying catalyst, reveals that the Krebs cycle could have hence emerged from a non-enzymatic precursor that forms spontaneously in the presence of sulfate radicals.
Experiments exploring the available chemical reaction space are constrained by combinatorics: the number of samples multiplies with each additional condition to be tested. To address this issue, we simplified and optimized sample preparation, LC-SRM measurement and statistical analysis for screening purposes at the expense of an exact rate determination. We then utilized more resource consuming methods for optimal chromatographic separation and absolute quantification of reaction rates in all subsequent verification experiments. This allowed us to measure a total of more than 4,850 samples along with 1,250 controls, external standards and blanks and to efficiently analyse and manually curate the corresponding ~65,000 LC-SRM chromatograms as specified below.
Each calculated reaction rate is based on a time series experiment with six collection points, which were performed in at least three replicates. Reaction rate was calculated only for those reactions that showed a significant product accumulation over time that was consistent in all three replicates. Consequently, for rate calculation of one reaction under a certain condition a total of 18 measurement points were used.
Sampling points in time course experiments were typically set to 0, 10, 30, 60, 120 and 300 min in order to cover both relatively fast and slow reactions. The reaction oxaloacetate -> pyruvate was the only reaction which was too fast for these timescales and we designed an alternative experimental setup with narrower time windows to follow this reaction.
Peaks were identified by matching retention time and fragmentation properties to externally measured chemically pure standards. Automated peak picking and integration of specific transitions by MassHunter (Agilent) was backed up by additional manual inspection of all peaks (see below). We controlled for cross-contaminations and carry-over by repeated measurement of blanks and substrate-free controls.
Metabolite standards were obtained at high purity. If not otherwise indicated, the product number refers to Sigma-Aldrich: sodium citrate (71635), sodium isocitrate (I1252), cis-aconitic acid (A3412), sodium α-ketoglutarate (K2010), sodium succinate (14160), succinic semialdehyde (Santa Cruz Biotechnology, F1114), sodium fumarate (F1506), L-malic acid (M6413), sodium pyruvate (P2256), oxaloacetic acid (O4126), iron acetate (FeAc, 339199), FeCl2 (372870), FeCl3 (157740), Fe(ClO4)2 (334081), Fe(ClO4)3 (309281), ferrocene (F408), FeS(268704), H3PO4 (P5811), 2-mercaptoethanol (Merck Millipore, 805740), cysteine (30095), DL-ethionine (E5139), dimethylsulfoxid (D8418), homocysteic acid (69453), NaHSO3 (Acros Organics, 41944), methionine (M9375), ammonium peroxydisulfate (Fischer Scientific, 10219790), sodium sulfite Na2SO3 (Fischer Scientific, 10070400), sodium sulfate Na2SO4 (Fischer Scientific, 10493372). All water was obtained commercially at UPLC-MS purity (Biosolve Chemicals, Cat no. 23214102).
For quantification of TCA intermediates an Agilent 1290 Infinity Binary LC system with an online coupled Agilent 6460 Triple Quadrupole Mass Spectrometer was used. Sample separation was achieved on a Zorbax Eclipse Plus C18 Rapid Resolution column (1.8 um, 2.1 x 50 mm, Agilent, column temperature 30°C). Solvent A contained 5% methanol, 0.2% acetic acid, 10 mM tributylamine in UPLC grade water (Greyhound) and Solvent B was 100% methanol (Greyhound). 1.5 - 2.5 µl of sample were injected on the column at 0.5 ml/min followed by gradient elution as detailed in UPLC Gradient Supplementary Tables 7-11. Needle wash to prevent sample carryover was performed by water:acetonitrile (2:1) containing FlushPort wash with each injection. Including washing and re-equilibration this resulted in total cycle times between 4.4 (4.15) and 16 min, depending on the gradient. (see gradients S7-11).
Mass spectrometric quantification of specific products was performed in multiple or selective reaction monitoring (MRM or SRM) mode. Instrument parameters and metabolite transitions for each feature were optimized using pure commercially available standards (Supplementary Tables 12-13). MS/MS data were analyzed with Masshunter Workstation (Agilent) using QQQ Quantitative Analysis Software package. All automatically integrated peaks were manually curated in order to ensure high data quality and consistency with regularly measured quality control standards. Repeatedly measured external standard dilution series were used for determination of absolute metabolite concentrations. Further analysis and fitting of reaction rates was performed in R (R Core Team, http://www.R-project.org).
For each replicate the recorded time series was used to determine product formation rates (time dependent accumulation of reaction products). Different fitting algorithms were used to account for varying modes of product formation, caused by dissimilar chemical properties of substrate, product, and co-products and other effects such as intermediate stabilities, reaction orders or reaction induced changes of the chemical environment. The models used were i) a least squares linear model for continuous product formation, ii) the nonlinear growth model y = a · −b·c being part of the SSgompertz module in R, iii) the maximum initial growth rate within the linear range using the least squares model to be used for products with dynamic formation/degradation behaviour iv) and an exponential decay model following the format y = a · 2(−b·x) + c. The best fitting model was chosen according to the respective R2 values and was confirmed by graphical, manual review of the plotted curves.
Differential raw peak area data (ΔXi = Xt=300 - Xt=0) between t = 300 min and t = 0 min were calculated from the individual LC-SRM peak areas extracted using the Masshunter software (Agilent) and were indicative for an accumulation of products (positive values) or the deletion of substrates (negative values). Assuming normal distribution we then calculated z-scores (zi) (for graphical representation see Supplementary Figure 5): with σ(X) being approximated by the median absolute deviation (MAD) according to: σ = MAD (X) · 1.4826. z-Scores were then converted into p-values using normal distribution function f(x) with μ = 0 and σ = 1:
100 µM of each individual TCA substrate were combined with a freshly prepared metal rich mixture (200 μM FeCl2, 10 nM CoCl2, 400 nM NiCl2, 10 nM MoO4 and 100 μM H3PO4) in a low-oxygen N2 atmosphere generated by three repeated vacuum/N2 gas cycles in an anoxic chamber (Coy Lab Products, USA). The mixtures were then sealed in HPLC glass vials (5182-0717 and 5182-0716, Agilent) and incubated at 70°C in a water bath. For all substrates other than oxaloacetate samples were collected after 0, 10, 30, 60, 120, and 300 min by rapid cooling on ice. This resulted in measurement of 486 samples plus controls. After incubation the reaction mixtures were transferred to 384-well plates (Greiner Bio-One, 781186) under normoxic conditions and stored at -80°C for subsequent LC-SRM measurement using the UHPLC gradient in Supplementary Table 7.
In order to determine the contribution of individual metals towards facilitating specific TCA metabolite interconversions we tested each of the constituents of the Archean sediment simulation for their catalytic potential. The same experimental setup as above was applied, using isocitrate and α-ketoglutarate as substrates and mixing them with each metal individually (200 μM FeCl2, 200 μM FeCl3, 10 nM CoCl2, 400 nM NiCl2, 10 nM MoO4, 100 μM H3PO4) under low-oxygen and in the case of Fe(III) normoxic conditions. Substrate and products in 324 sample plus controls were measured with the LC-SRM method using UHPLC gradient S8.
Reaction mixtures containing oxaloacetate were generated by combining oxaloacetate with FeCl2 at the same concentrations as stated above but under normoxic conditions, directly followed by incubation at 40°C in the autosampler of the Agilent 1290 HPLC system. Instead of stopping the reaction on ice the HPLC was programmed to automatically inject 1.5 µl of the sample onto the column every 5 min for up to 2.5 hrs. The three replicates for the FeCl2 condition and the iron-free control were measured in alternating order. Substrates and products in 113 samples plus controls were measured with a LC-SRM method using the UHPLC gradient in Supplementary Table 8.
In order to determine the effects of pH on ferrous iron induced non-enzymatic reactivity the interconversion experiments were carried out in the presence of 5 mM sodium phosphate buffering at pH points 3, 5, 6, 7, 8, and 9 in analogy to the experiments described in 17. Furthermore the reaction mixture consisted of 100 μM isocitrate (or water as control) and 200 μM iron(II) chloride (Sigma-Aldrich, 372870). The correct starting pH was controlled for by initial measurement, and kept constant throughout the incubations via the buffer capacity of the respective buffer. Substrates and products in 252 samples plus 56 controls were measured with a LC-SRM method using the UHPLC gradient in Supplementary Table 9.
For screening of iron and/or sulfur species that actively promote non-enzymatic reactivity among TCA metabolites the experimental setup was adapted to be performed in 96-well format. Samples were prepared in glass-coated 96 well plates (96 PLATE+ 7MM RD U 300UL PP, Thermo Scientific), sealed in low oxygen conditions and additionally vacuum-packed to prevent any possible well to well cross-contamination. 100 µM citrate, cis-aconitate, succinate, malate and fumarate were used as substrate individually and mixed with all possible combinations of 200 µM of different iron sources (FeAc, FeCl2, FeCl3, Fe(ClO4)2, Fe(ClO4)3, ferrocene, FeS and iron-free controls) and 200 µM of inorganic or organic sulfur species (2-mercaptoethanol, cysteine, DL-ethionine, dimethylsulfoxid, homocysteic acid, NaHSO3, methionine, (NH4)2S2O8, Na2SO3, Na2SO4 and sulfur-free controls). The samples were heated to 70°C in a water bath for 0 and 300 min. This resulted in a total of 1320 samples plus controls. Samples were then transferred to 384-well plates (Greiner Bio-One, 781186) under normoxic conditions and stored at -80°C for subsequent LC-SRM measurement using the UHPLC gradient in Supplementary Table 10.
On the basis of the statistical analysis of the iron/sulfur screening results we selected the most potent non-enzymatic interconversion conditions and verified them in time series experiment with three replicates using a comprehensive targeted mass spectrometric quantification method. The substrates citrate, isocitrate, cis-aconitate, α-ketoglutarate, succinate, succinic semialdehyde, fumarate and malate were diluted to 100 µM in UPLC grade water and mixed with 200 µM peroxydisulfate in the presence of absence of 200 µM ferrous sulfide (FeS). In analogy to the experiments above these mixtures were sealed under anoxic conditions and were incubated at 70°C in a water bath. Samples were collected after 0, 10, 30, 60, 120 and 300 min by rapid cooling on ice, resulting in 432 samples plus controls, which were transferred to 384 well plates and stored at -80°C for subsequent LC-SRM analysis using the UHPLC gradient in Supplementary Table 11.
Recovery rates were quantified via the quotient of the respective TCA metabolites at timepoint t=0 and the total sum of concentrations measured after 2 hours of incubation at 70°C. The fraction of products at timepoint t=2 hours compared to the total sum of TCA metabolites (substrate + products) was calculated to determine the percentage of specific TCA products. Please note, the absolute quantification of citrate in presence of peroxydisulfate (and with it the calculated recovery rate) is hampered by an unusually high variance (CV = 25.6%) for this metabolite due to an unknown 20 mechanism/ chemical interference (the average variance for all other features, metabolites, and recovery rates remains low (CV = 3.48%). For this technical reason, the recovery rate calculated for citrate and the efficiency of the reactions that start with citrate, have a higher uncertainty according to this CV value.
In order to investigate the potential contribution of sulfur radical species to the non-enzymatic reactivity facilitated by peroxydisulfate we compared them to hydroxyl radicals generated from hydrogen peroxide. In three replicates we incubated 100 µM citrate, isocitrate, cis-aconitate, alpha-ketoglutarate, succinate, fumarate and malate with 200 µM hydrogen peroxide or 200 µM peroxydisulfate at 70°C under anoxic conditions and collected samples after 0, 10, 30, 60, 120 and 300 min (378 samples plus controls) and measured them by LC-SRM analysis using the UHPLC gradient in Supplementary Table 11.
The differential radical scavenging properties of 2-propanol and tert-butanol were exploited to test for the importance of sulfate over hydroxyl radicals. In these experiment 200 µM peroxydisulfate was mixed with 100 µM citrate, isocitrate, cis-aconitate, α-ketoglutarate, succinate, fumarate or malate individually and each combination was treated with 500 µM 2-propanol, 500 µM tert-butanol or water as a control. Samples were sealed under anoxic conditions, heated to 70°C in a water bath and incubated for 0, 10, 30, 60, 120 and 300 min (504 samples plus controls) and then measured by LC-SRM analysis using the UHPLC gradient in Supplementary Table 11.
We thank George Averill and Timo Littmann for helping with experiments. This work was supported by the Francis Crick Institute which receives its core funding from Cancer Research UK (FC001134), the UK Medical Research Council (FC001134), and the Wellcome Trust (FC001134), the Wellcome Trust (RG 093735/Z/10/Z to MR), and the ERC (Starting grant 260809 to MR) for funding. MAK is supported by an Erwin Schrödinger postdoctoral fellowship (FWF, Austria, J3341). DK is supported by an Ad Futura studentship (Slovene Scholarship Fund).
Author ContributionsM.A.K. and M.R. designed the research; M.A.K., D.K. and S.A.H. performed the research; M.A.K and M.R. wrote the first draft of the paper, and all authors contributed to finalizing the manuscript.
Competing financial interests
The authors declare no competing financial interest.