ABSTRACT Chemical complexity is vital not only for the origin of life but also for biological evolution. The chemical evolution of a complex prebiotic mixture containing acetylene, carbon

monoxide (CO), and nickel sulfide (NiS) has been analyzed with mass spectrometry as an untargeted approach to reaction monitoring. Here we show through isotopic 13C-labelling, multiple

reaction products, encompassing diverse CHO and CHOS compounds within the complex reaction mixture. Molecules within the same chemical spaces displayed varying degrees of 13C-labelling,

enabling more robust functional group characterization based on targeted investigations and differences in saturation levels among the described classes. A characteristic C2-addition pattern

results give an essential insight into the still elusive role of sulfur dynamics in the origin of life. Moreover, our results provide temporally resolved evidence of the progressively

increasing molecular complexity arising from a limited number of compounds. SIMILAR CONTENT BEING VIEWED BY OTHERS NICKEL-ORGANO COMPOUNDS AS POTENTIAL ENZYME PRECURSORS UNDER SIMULATED

EARLY EARTH CONDITIONS Article Open access 15 February 2024 SYNTHESIS OF PREBIOTIC ORGANICS FROM CO2 BY CATALYSIS WITH METEORITIC AND VOLCANIC PARTICLES Article Open access 25 May 2023

ANAEROBIC OXIDATION OF PROPANE COUPLED TO NITRATE REDUCTION BY A LINEAGE WITHIN THE CLASS SYMBIOBACTERIIA Article Open access 17 October 2022 INTRODUCTION In 1953, Reppe pioneered the

synthesis of fatty acids from acetylene and carbon monoxide1. In conjunction with a nickel carbonyl catalyst, both gases yielded acrylic acid and longer unsaturated fatty acids. However,

nickel carbonyl, a water-labile compound, is not the only catalyst capable of lowering the required energy to accelerate this reaction. Recently, this reaction was reinterpreted in an

origin-of-life context as fatty acids play structural and energetic roles in living organisms. Experimental evidence that describes the formation of a variety of fatty acids of different

lengths and degrees of saturation was achieved under volcanic hydrothermal conditions, utilizing a nickel sulfide catalyst compatible with aqueous early earth conditions2. So far, acetylene

has been underrepresented in origin-of-life research. Literature is scarce, but new evidence for its relevance emerges. Acetylene is formed from methane irradiated by UV light3. Multiple

planetary bodies show an atmosphere partially made from acetylene gas, like the Saturn moon Titan4,5 and the Jovian planet Jupiter6. The atmosphere of Enceladus, another moon of Saturn,

contains acetylene in addition to phosphorous7 and exhibits hydrothermal volcanic activity8. The existence of acetylene in the atmosphere of early Earth was also hypothesized9 and can be

found nowadays in fumaroles of geothermal areas10. Spark discharge experiments of gaseous nitrogen and methane mixtures also lead to the formation of acetylene11. Extant microorganisms in

anaerobic aqueous environments can use acetylene as an energy and carbon source, increasing the likelihood of its presence at early evolutionary stages. Specifically, _Pelobacter

acetylenicus_ can grow from acetylene12 alone and therefore demonstrates that acetylene has the potential to fuel a complete metabolism on its own. Acetylene is transformed into

acetyl-coenzyme (Co)A, a thio ester, via the hydration of acetylene into acetaldehyde. Acetyl-CoA is then used to build metabolites with C2-units. The role of sulfur in the origin of life is

still an elusive and extensively researched topic. Undoubtedly sulfur is essential for extant life, as it is part of methionine and cysteine, acetyl-CoA, and multiple hydrogenases13.

Popular hypotheses for the origin of life also include sulfur as a critical element in a more indirect way. Inspired by the “iron-sulfur world” theory of Wächtershäuser14, transition-metal

sulfides were used as catalysts in origin-of-life experiments. This theory proposed a mineral surface metabolism, starting from simple inorganic precursors and evolving into complex

bioorganic molecules. This hypothetical chemoautotrophic evolution proceeds _via_ thio acids or thioesters in reductive autocatalytic cycles15. Incubation of carbon monoxide with methyl

mercaptan over transition-metal sulfides leads to the well-coveted activated thioester16, a molecular part of acetyl-CoA. These seminal results sparked the discovery of other reactions,

possible in a hydrothermal environment and yielding prebiotically-relevant compounds, including acetaldehyde17, Krebs cycle intermediates18, and the porphyrin building block pyrrole19. De

Duve proposed a second hypothesis, heavily depending on sulfur compounds where thioesters contribute the energy for essential reactions20. Moreover, thiols were described as a possible

prebiotic intermediate for peptide-bond formation21, whereas sulfur-containing heterocycles could act as catalysts for biologically-relevant reactions22. A deeper comprehension of chemical

complexity is vital not only for the origin of life but also for biological evolution. We combined 13C-labelling with untargeted ultrahigh-resolution mass spectrometry to tackle the

challenging analysis of highly complex evolving abiotic systems. We describe an analytical approach based on known chemical reactions that allows us to categorize detected elemental

compositions into individual compound classes via the degree of 13C-labelling. In this study, we expanded our knowledge of the diversity of compound classes formed from prebiotically

relevant gases. We recognized C2-addition as a driving factor for compound diversity in a given compound class. In addition, we identified new functional classes, such as thio ethers and

thio acids. Through labeling, we discovered that there are two pathways leading to thio acids, which are crucial molecular components of acetyl-CoA. Thioacids formed solely from acetylene

also enabled comparison with Pelobacter acetyleneicus. Lastly, this approach succeeded in detecting a sulfur-specific trend that led to the reduction of sulfur atoms per molecule after the

initial introduction of sulfur to the gases. This trend led to compounds with low numbers of sulfur, more aligned with biomolecules in extant organisms, shedding light on sulfur dynamics in

abiotic systems. RESULTS COMPOSITIONAL COMPLEXITY INCREASES OVER TIME We incubated acetylene with carbon monoxide over water containing nickel sulfide for varying time periods at 105 °C and

measured the evolving mixture at different time points. After 2 h, the first signals belonging to reaction products were analyzed by direct infusion Fourier transform ion cyclotron resonance

mass spectrometry (FT-ICR-MS). Longer incubation times increased the chemical diversity and complexity of organic compounds, meaning a functional and compositional variety of molecules.

Visualization of the increasing diversity of elemental CHO and CHOS compositions found in the one-pot reaction can be seen in Fig. 1. The mass-to-charge ratio was plotted against the

hydrogen-to-carbon ratio. This separation allowed an overview of the chemical composition of the system resolved by the mass and the degree of saturation of the individual compounds. We

separately focused on the chemical space of CHO and CHOS compounds. We observed an increase in detected signals over time for both chemical spaces, strongly suggesting a diversification of

reaction products by a factor of ~9. The main group of the detected compounds is highly unsaturated, as the average H/C ratio is 1.4 for both chemical spaces after 7 days. This strong bias

toward unsaturated compounds is in line with the utilized reactants (acetylene possessing a triple bond) and targeted GC-MS measurements of formed highly unsaturated carboxylic acids in the

mixture2. Further, the mass of the compounds increased over time. The overall diversity increases as well, as the number of detected CHO and CHOS compounds increases from 328 annotated

signals after 2 h to 2885 annotated signals present after 7 days. The compositional space visualization of the ongoing reactions gives an overview of the system, but elemental compositions

alone do not provide information about isomers and, more importantly, functional groups. The determination of such functional groups remains a determining factor if specific reactions need

to be characterized. RESOLVING FUNCTIONAL DIVERSITY BY 13C-LABELLING Comparing unlabeled setups to setups with 13C-labelled carbon monoxide allowed us to characterize functional groups and

compound class diversity better. Categorizing the elemental annotations by 13C-labelling improved the amount of information, where 13C-carbons convey specific functional insights into the

onset of an early evolving system. This additional dimension allowed us to resolve different compound classes with the same number of heteroatoms. The origin of the label (carbon monoxide in

our experimental setup) provided insight into the functional groups present in elemental subspaces after chemical reactions. Targeted GC-MS analysis of this mixture revealed that carbon

monoxide is mainly reacted into a carboxylic acid group2, in agreement with Reppe´s chemistry1. In line with published data2,18, we were able to differentiate distinct populations of CHO and

CHOS compounds in our model, as some compounds are labeled once, twice, or higher. CxHyO3-compounds form the first elemental composition with more heteroatoms than pure fatty acids (Fig. 

2). The elemental compositions with a single 13C-label show a saturation level on average higher (1.38) than the saturation of the double-labeled compositions (1.20). This result strengthens

the hypothesis that carbon monoxide is introduced as a carbonyl group. The carbonyl group reduces the H/C ratio compared to a hydroxy group or ether. Mono-labeled compounds, therefore,

belong to carboxylic acids carrying an additional hydroxy or ether group. The addition of water to a double bond is likely responsible for the increase in oxygen in molecules without the

need for carbon monoxide. We further observed that the number of oxygens in compounds with one 13C label positively correlates with the H/C ratio of the detected compounds, further

strengthening the claim that the introduction of oxygen via water consumes a double bond (supplementary fig. 1). These results suggest a separation of the CHO3 space into keto acids and

either hydroxy acids or carboxylic acids with an ether (cyclic unsaturated ethers like furans, for example). Similar carboxylated heterocycles with sulfur, namely thiophenes, were already

described in the system23. The recurring pattern of molecules reflecting C2-addition originating from acetylene is important to mention. Compounds of a specific subspace with the same amount

of 13C label increase in mass only via the addition of acetylene or reduction of double bonds. This addition of C2-units is reminiscent of the C2-metabolism carried out by acetyl-CoA. This

behavior of mass increase via acetylene can be seen for all identified compound classes. Additional heteroatoms increase the number of potential isomers and functional groups. This labeling

approach further allows distinguishing at least three different compound classes in the CHO4-subspace (Fig. 3). Mono-labeled compounds show the expected behavior of an increase in H/C-ratio

compared to the CHO3-subspace (from 1.38 to 1.57). This is the result of the consumption of a double bond during the introduction of water into the molecule. The mono-labeled compounds

belong to the group of dihydroxy-acids and were not yet described in the system. Double-labeled compounds present a challenge, as the labeling still allows the formation of dicarboxylic

acids or hydroxy-keto acids. The information that carbon monoxide is converted into a carbonyl group is insufficient for categorization. Further categorization requires the inclusion of an

additional element, namely sodium. Our data suggested that dicarboxylic acids are prone to form sodium adducts after negative electrospray ionization. A double-deprotonated species can carry

a positively charged sodium ion while still being negatively charged. This observation allows for the separation of double-labeled compounds into two potential subgroups. Compositions

labeled twice and showing sodium adducts can be categorized as dicarboxylic acids. The presence of succinic acid in the system was already shown in a previous publication18. Notably, no

annotations with a single label (tentatively one carboxylic group) and a sodium adduct are detected. The same applies to the triple-labeled compounds that will be discussed later. This fact

strengthens the hypothesis that this behavior is specific to dicarboxylic acids in the CHO4 subspace. A further sign of the occurrence of dicarboxylic acids is the strongly increased average

H/C ratio (1.39) of compounds falling into this category compared to the average of this class (1.27). The introduction of a further carboxylic group consumes a double bond if the

underlying mechanism complies with the reaction hypothesis of Reppe. This consumption of a double bond would raise the saturation level of the compounds and explain the strong deviation from

the remaining double-labeled annotations. The categorization is still ambiguous, as compounds with higher mass may lead to reduced formation of sodium adducts. Notably, all sodium adducts

are detected in a lower mass range than non-sodium-adduct-forming compounds. Strong evidence, however, for the presence of a mix of dicarboxylic acids and hydroxy-keto acids in the

double-labeled CHO4-subspace is the fact that a triple-labeled group is present. No sodium adducts are observed in this group, and the H/C ratio is, on average, lower (1.15). These results

strengthen the annotation as diketo acids and make the presence of hydroxy-keto acids for double-labeled compounds more likely. CHO5 and CHO6 subspaces follow the same trends described for

the previous subspaces. Compounds containing sulfur show similar patterns. The CHO1S1 is the first elemental subspace in the category of CHOS compounds. Our results distinguished two groups

(Fig. 4). Unlabeled compounds originate from acetylene alone, whereas mono-labeled compounds are derived from acetylene and a single carbon monoxide molecule. No double- or triple-labeled

CHO1S1 compounds were detected. CHO1S1 compounds match the elemental composition of thio acids. The possibility of a modified Reppe chemistry with hydrogen sulfide instead of water leading

to thio acids was already shown in earlier works of Reppe1. Having both labeled and unlabeled species of this compound class is surprising, as the pathway described by Reppe requires carbon

monoxide. However, the probability that the unlabeled compounds belong to a different class of compounds is low, as hydroxy and thiol groups alone do not efficiently ionize in negative

ionization mode. Those unlabeled species are also mostly fully labeled if acetylene is used with two labeled carbons instead of carbon monoxide (Fig. 4, black circled dots), excluding

contamination. The formation of thio acetic acid could be detected in high amounts at early time points in the system with NMR (see Supplementary Fig. 2), further strengthening the presence

of thio acids formed without carbon monoxide. If no more than two oxygen atoms are present in the molecule, the amount of labeled carbon does not exceed one 13C. This result suggests that

sulfur cannot completely exchange oxygen in this system. Oxygen originating from carbon monoxide stays attached to its labeled carbon. The increased number of hetero atoms in the CHOS

subspaces progressively leads to ambiguity. Relevant information can still be gained from 13C labeling. The CHO3S subspace behaves similarly to the CHO3 rather than the CHO4 subspace. Only

mono- and double-labeled compounds can be detected. In addition, no sodium adducts are detected. This result suggests that compounds carrying a carboxylic and a thiocarboxylic acid group

simultaneously are absent from the system. CHO4S is similar in this regard. The diversity in sodium adducts for this subspace exceeds the diversity of the non-sodium-adduct-forming fraction

of double-labeled compounds. However, the complete absence of triple-labeled compounds is very surprising in this subspace, likely because double-labeled CHO4S belong to thioethers. Two

carboxylic acids are linked to each other via a sulfur ether. To further strengthen this claim, the detected elemental composition of C6H10O4S was identified and validated as

thiobispropanoic acid via targeted GC-MS analysis by comparing retention time and the fragmentation pattern to a commercially available standard (Supplementary Fig. 3). Adding one sulfur to

reach the CHO4S2 subspace shows only double-labeled sodium adducts as a coherent homologous series. The result suggests the presence of two carboxylic acids linked by a sulfur bridge,

reminiscent of protein sulfur bridges allowing their tertiary structure (Supplementary Fig. 4). Further interpretations of higher heteroatom combinations were deemed too ambiguous, but a

table showing all annotations with the corresponding labels can be found as a supplementary Excel sheet (Supplementary Data 1). One source of ambiguity is the presence of “mixed” 13C

annotations where the same elemental composition is present in different degrees of 13C labeling. Due to this, it is almost impossible to reliably assign functional groups to a detected

signal. However, it is still interesting to investigate how the percentage of “mixed” annotations changes for different subspaces in such a complex mixture. A reaction scheme summarizing all

proposed mechanisms and 13C-patterns can be found in S.I. (supplementary fig. 5). ISOMER FREQUENCY HAS AN UNPREDICTABLE VARIANCE IN ANALYZED SUBSPACES 13C labeling of the sample allowed

additional dimension for untargeted analysis, which is otherwise inaccessible in direct-infusion mass spectrometry. The labeling revealed that some of the identical elemental compositions

existed as a mixture of 13C labeled species, as labeled experiments yielded signals compatible with multiple degrees of labeling. A representative comparison between labeled and unlabeled

spectra can be found in S.I. (supplementary fig. 6). We investigated the percentage of mixed and pure annotations for different chemical subspaces and observed unexpected behaviors. With an

increasing number of hetero atoms, we expected a steady increase in the fraction of mixed annotations compared to pure annotations. This, however, was not always the case. The CHO space

showed an increase of mixed annotations from two (7.7%) to three (17.4%) oxygens per molecule. The CHO4-subspace, however, only shows 12.9%, and the CHO5 subspace 4.9% of mixed annotations.

The CHOS space showed increased mixed annotations compared to the CHO space. However, no clear trend could be elucidated. CHO1S1 and CHO2S3 showed 0% mixed annotations, in contrast to

CHO3S2, with 39% mixed annotations. These results highlight the unpredictability of isomer populations in untargeted FT-ICR-MS. Using 13C labeling allows a definite distinction between

impurities and experimental sample components24. This result is difficult to achieve with FT-ICR-MS, as removing blank signals potentially removes specific results corresponding to compound

isomers in solvents or other sources of contamination. In some instances, compounds like fatty acids can be in the solvent and the investigated system. TEMPORAL EVOLUTION OF THE SYSTEM The

system was visualized over time via a temporal molecular network (Fig. 5). In this network, individual nodes represent detected annotated signals. Overall, 6 elemental compositions were

chosen as possible edges, all representing differences in molecular weight after specific reactions. Based on previous publications or available reactants, the 6 chosen mass differences

(Table 1) represent possible reactions likely to happen in the system. Edges can represent the addition of acetylene25, the simultaneous addition of carbon monoxide and water to a double or

triple bond to form a carboxylic acid group. The same reaction can be slightly altered with hydrogen sulfide instead of water resulting in a thio acid1. The addition of water26, hydrogen

sulfide27, or hydrogen represents the loss of a double or triple bond, potentially through reduction. This limited number of possible edges allowed to interconnect 97.5% of all annotated

signals. The overall temporal path taken by the system is visualized by a molecular network (Fig. 5A). Molecular networks and mass-difference analysis were developed for biological samples28

and used in recent untargeted investigations of astrochemical reactions29 allowing a comprehensive overview of the chemical system. The masses increase over time, and later detected

molecules show the highest masses (>500 u) (Fig. 5B). The amount of hydrogen and carbon follow a nearly identical trend compared to the mass (Fig. 5C and D). The percentage of compounds

containing high numbers of sulfur atoms per molecule (>2) sulfur) is highest at early time points (Fig. 5F). The percentage of CHOxS3 annotations starts at 29% of overall sulfur

annotations after 2 h and is lowered to 17% after 7 days, even though the absolute amount of CHOxS3 annotations is increasing (from 60 annotations after 2 h to 388 after 7 days). CHOXS4

compounds start at 39 annotations after 2 h and go down to 22 after 7 days (from 17 to 1% of total CHOxS4 annotations). The CHOxS5-subspace disappears completely after 3 days. Compounds

annotated with 1–2 sulfur show the opposite trend. The percentage of CHOxS1 increases from 27% to 44.5% over the time of the experiment. We observe an inverted picture for the relative

abundance of CHO compounds. CHO compounds with 2–3 oxygen represent 27–34% of all CHO annotations after 2 h of incubation. This percentage is reduced to 13–15% after 7 days of incubation. We

have further used self-organizing maps (SOM) classification theory30 to characterize time-dependent molecular profiles in greater detail. This technique allows the clustering of temporal

mass abundance profiles that follow the same evolutional trend over time. Masses following a similar intensity change over time are clustered together. The approach was already successfully

used in other untargeted FT-ICR-MS analyses to categorize the temporal evolution of detected mass signals31 in food samples. Our results show 8 different main clusters (Fig. 6). These

clusters show groups of masses reaching their maximum intensity at different time points. We can confirm two trends that were suggested in the temporal network.: Clusters with maximum

intensity at earlier time points show elemental compositions with lower masses on average than elemental compositions in clusters with late maxima. Compounds with higher amounts of sulfur

reach their intensity maximum earlier than compounds with less sulfur. This fact shows that the continuous addition of sulfur to the unsaturated olefinic molecules is unlikely. The profiles

of the different groups give insight into the changing reactions over time, as compounds do not all linearly accumulate in the system but have different peak times. Some compounds are mostly

depleted after 7 days (Fig. 6A, B, D). The behavior of sulfur over time is particularly interesting (Fig. 7). Sulfur-containing compounds with 3 or 4 sulfur atoms appear earlier and degrade

quickly (Fig. 7A, B). The peak time appears later for annotations with lower numbers of sulfur (Fig. 7C, D). This effect differs for CHO compounds, where the compounds have a peak time of 7

days (or later) and mostly show steady signal increases over time. Based on our results, the addition of acetylene or other mass-increasing reactions compensates for the loss of mass due to

lower amounts of sulfur. However, an exchange of sulfur through other mass-increasing building blocks can only be hypothesized. 84% of all annotated thio acids follow the trend of cluster 6

(Fig. 6H). The observed behavior of the higher mass thio acids is different from their low mass counterpart thio acetic acid, which is present after 2 h in high amounts and then reacts away

throughout the experiment (supplementary fig. 2), partially by hydrolyzing to acetic acid. DISCUSSION The described system demonstrated its potential in previous publications to produce

different prebiotically-relevant substances like aldehydes, fatty acids, and thiophenes2,17,23. The formation of pyrrole19 and amino acids from aldehydes17 via the Strecker reaction was also

demonstrated in previously published experiments that included nitrogen. Our study now expands these targeted observations to reveal a dynamic chemical landscape of functional groups

derived from basic building blocks, emphasizing sulfur-containing molecules and the deconvolution of functional groups with the help of 13C labeling. The size of the investigated molecules

also continues to grow progressively over time, mainly via a C2-unit increase, reminiscent of the C2-metabolism including the formation of fatty acids, polyketides, and terpenes from

acetyl-CoA units in extant organisms32. Some prokaryotes even use acetylene as a main carbon source for their metabolism. The Gram-negative bacterium _Pelobacter acetylenicus_ lives in

anoxic oceanic sediments and converts acetylene into acetyl-CoA via acetaldehyde to fuel its C2-metabolism12. Capitalizing on our previous findings of a primordial conversion of acetylene

into fatty acids and related organic molecules, this primitive bacterium could therefore be seen as the link between a purely abiotic acetylene-based C2-metabolism and the C2-metabolism in

extant organisms. The formation of acetaldehyde and thio acetic acid S-methyl ester (a simple analog to acetyl-CoA) from acetylene was already shown in this system16,17. Isotope labeling

uncovered the system’s hidden diversity in functional groups. We could separate functional groups with the same number of hetero atoms by FT-ICR-MS. Separating functional groups with the

same number of hetero atoms is difficult for FT-ICR-MS-based analysis. The problem could be solved by 13C isotope labeling of the starting materials. This approach made it possible to trace

the origin and chemical nature of hetero atoms based on the literature1,18,25. The CHO3-subspace shows hydroxy acids and keto acids. Hydroxy acids continue to gain interest in the

origin-of-life field. α-hydroxy acids can enhance peptide-bond formation in dry-down reactions33, even though our analysis does not allow for the exact identification of the position of the

functional group. The same can be said of keto acids, which play a central role in an ancestral analog of the Krebs cycle34,35. Dicarboxylic acids gained recent attention due to their

ability to form co-polymers with glycol nucleic acids with a hypothesized potential to perform genetic or catalytic functions36. The diverse compound classes from multiple species have

already proven to be significant in the origin of life. After the primary introduction of varying amounts of sulfur to the initial reactants, we observed a percentual decrease of sulfur

atoms per molecule over time instead of a continuous increase. This decrease in sulfur is true for all sulfur-containing groups that could be resolved and categorized in this study. The

behavior of sulfur differs from that of the other elements in the system. The disappearance of sulfur from the formed compounds is an interesting observation. Sulfur represents an important

element for origin-of-life reactions. In extant organisms, sulfur is less abundant than other relevant elements like carbon, nitrogen, and phosphate. Nonetheless, the remaining sulfur plays

a crucial role in extant organisms. Indeed, thioesters like acetyl-CoA belong to the metabolically essential sulfur molecules. It is challenging to provide conclusive evidence for the

precise process that leads to a sulfur reduction in the resulting compounds. Still, it can only be hypothesized with this untargeted approach. We conducted and analyzed a 7-day experiment to

study the evolution of a system with progressively decreasing sulfur levels. This system can be considered a fast motion of early evolution on Earth. The analysis of the fraction of isomers

revealed an unexpected distribution. Instead of a steady increase in isomer diversity, some chemical subspaces, mainly the sulfur-containing ones, showed very high variance in mixed

annotations. This result shows an unknown amount of directed synthesis in the system, as some subspaces keep a certain amount of functional purity and do not uncontrollably diversify over

time. It is also relevant to mention the presence of thio acids in a large diversity. The present investigation reveals the full extent of the possible molecular diversity of pure thio acids

and describes different formation pathways. One pathway requires acetylene and carbon monoxide; the other relies on acetylene alone. Independent of the pathway, the increase in mass and

many saturation levels remain comparable. The temporal analysis of the mixture also revealed that larger thio acids reach their maximum intensity much later than thio acetic acid, most of

them belonging to the SOM cluster reaching a maximum after 3 days. Thio acetic acid, on the other hand, decays quickly and becomes undetectable via NMR after 8 h. Acetylene is the main

driver of the increased mass of the detected molecules. Labeled atoms stemming from carbon monoxide remain in the single digits independently of the size of the molecule. Compounds detected

after 7 days show between 15 and 27 carbon atoms within the mass range of 230–500 m/z but present only up to four carbon labels from 13CO. Acetylene is still a building block often

overlooked. Still, our finding turns it into an important tool to increase molecular mass or as a C2-spacer to optimize the spatial arrangement of functional groups. All compound classes

exhibit a noticeable increase in two-carbon mass, known as C2-chemistry. This phenomenon closely resembles the C2-metabolism of contemporary organisms, which is mediated by acetyl-CoA.

CONCLUSION This work revealed a new dimension of complexity in a hydrothermal system based on the “metal-sulfur” world theory. Utilizing isotope labeling to categorize the functional groups

enhanced the understanding of the reactions in the system. Unexpected behavior was observed for sulfur, as its number was lowered in detected compounds over time, leading to sulfur numbers

more akin to the biological molecules in contemporary organisms. We have discovered several ways to produce thio acids, indicating that this group of compounds is easily accessible in the

environment we investigated. Furthermore, the role of acetylene as the main building block for synthesizing higher-mass compounds was shown by differentiating carbon originating from carbon

monoxide and acetylene. We revealed a reoccurring pattern of C2-addition to all formed compounds through acetylene, a nutrient used by _Pelobacter acetylenicus_ to fuel its fatty acid

synthesis via a similar C2-metabolism. These results show new paths for further investigations that require the described functional groups or deliver a framework to tackle the analysis of

even more complex systems containing nitrogen or phosphor. METHODS REACTION BOTTLE SETUP In a typical run, a 125 ml glass serum bottle was charged with 1.0 mmol NiSO4 • 6 H2O (99%, Aldrich)

and sealed with a silicon stopper. The bottle underwent three cycles of evacuation and argon filling, ultimately reaching a deaerated state. Subsequently, the bottle was filled with

argon-saturated water (calculated for the end volume of 5 ml), with 1.0 mL argon-saturated 1 M Na2S (solid Na2S: 99.99%, Aldrich) solution, with 1.0 mL 1 M NaOH solution and finally with 60 

ml unlabeled CO and 60 ml unlabeled acetylene (acetone-free), using gastight syringes for the injections. Reactions were carried out at 105 °C. Following a reaction time of up to 7 days, the

reaction mixture was cooled down. To conduct labeling experiments, 13CO was utilized, while in a control run with the same composition, acetylene and CO were substituted with argon. FT-ICR

MASS SPECTROMETRY Samples were taken from the serum bottle with a syringe and centrifuged for 5 min at 15000 _rpm_. 100 µl of the supernatant were diluted in 900 µl methanol and centrifuged

again to remove the precipitated salt. 70 µl of the centrifuged sample were diluted again in 930 µl methanol. For the timepoints 2 h, 1 day, 2 days, 3 days, 7 days and 7 days (13 C labeled)

three different bottles were analyzed as biological replicates. Time points 3 h to 20 h were measured with two biological replicates. Every biological replicate was measured as three

technical replicates. Only signals appearing in >66% of a triplicate were kept for annotation. Only annotated signals with a H/C ratio between 0.5 and 2.5 were kept. O/C ratios had to be

below 1.5 for all annotations. Analysis was performed on a high-field Fourier Transform Ion Cyclotron Resonance mass spectrometer from Bruker Daltonics—Solarix with a 12 T magnet from

Magnex. The mass spectra were acquired with a 4-megaword (MW) time domain. The system was calibrated with L-Arginine clusters in negative ionization mode (5 mg L−1 L-arginine solved in

methanol). For each sample, 200 scans were accumulated in negative ion mode in the mass range of 122–1000 amu. Ions were accumulated for 300 ms. The pressure in the hexapole was 3 × 10−6

mbar, and the pressure in the ICR vacuum chamber was 6 × 10−6 mbar. An Apollo ii (Bruker Daltonics) ESI source was used. The supernatant was injected via a microliter pump system (flow rate:

120 µl h−1). Data were recalibrated post data collection via a calibration list based on fatty acids with different chain lengths. Peaks were picked automatically in Data Analysis (Bruker)

with a s/n threshold of 4. Mass lists were exported, filtered with two in-house filters removing wiggles artifacts and natural 34 S isotopes. Formula assignment was done through a mass

difference network approach37. The transformation list can be found in the excel sheet supplementary data. Annotation of the labeling degree was done by comparing the 7-day setup with a

CO-13C- or acetylene 13C labeled 7-day setup. In CO-labeled setups, compounds were categorized as labeled if the corresponding signal in the labeled sample showed a signal that surpassed the

expected signal intensity of the natural 13C (1% times the number of carbon atoms in an elemental composition) by 100%. 13C acetylene signals were checked manually and had to fulfill the

same requirements. Molecular networks were generated and analyzed via the method mol2net (https://zenodo.org/record/7025094; Ruf & Danger 2022). SOM-CLUSTERING The data were preprocessed

by the sklearn MinMaxScaler function. The SOM model was implemented on a 2 × 4 grid with a learning rate of 0.1. A Gaussian neighborhood function on top of a rectangular topology was used.

Euclidean activation distances were used for model calculations. The compiled model was trained for 50,000 iterations. Aggregated clusters were extracted from the winning map and plotted

with respective averaged cluster centers. DATA AVAILABILITY The authors declare that [the/all other] data supporting the findings of this study are available within the paper [and in

Supplementary Data 1]. Further data that support the findings of this study are available from the corresponding author upon reasonable request. REFERENCES * Reppe, W. Carbonylierung I. Über

die Umsetzung von Acetylen mit Kohlenoxyd und Verbindungen mit reaktionsfähigen Wasserstoffatomen Synthesen α,β-ungesättigter Carbonsäuren und ihrer Derivate. _Justus Liebigs Ann. der

Chem._ 582, 1–37 (1953). Article  CAS  Google Scholar  * Scheidler, C., Sobotta, J., Eisenreich, W., Wächtershäuser, G. & Huber, C. Unsaturated C3,5,7,9-Monocarboxylic Acids by Aqueous,

One-Pot Carbon Fixation: Possible Relevance for the Origin of Life. _Sci. Rep._ 6, 27595 (2016). Article  CAS  PubMed  PubMed Central  Google Scholar  * Ormeland, R. S. & Voytek, M. A.

Acetylene as Fast Food: Implications for Development of Life on Anoxic Primordial Earth and in the Outer Solar System. _Astrobiology_ 8, 45–58 (2008). * Abbas O. & Schulze-Makuch D.

Acetylene-based pathways for prebiotic evolution on Titan. _Exo-Astrobiology_ 518, 345–348 (2002). * Cable, M. L., Vu, T. H., Maynard-Casely, H. E., Choukroun, M. & Hodyss, R. The

Acetylene-Ammonia Co-crystal on Titan. _ACS Earth Space Chem._ 2, 366–375 (2018). Article  CAS  Google Scholar  * Melin, H., Fletcher, L. N., Irwin, P. G. J. & Edgington, S. G. Jupiter

in the Ultraviolet: Acetylene and Ethane Abundances in the Stratosphere of Jupiter from Cassini Observations between 0.15 and 0.19 μm. _Astronom. J._ 159, 291 (2020). Article  CAS  Google

Scholar  * Postberg, F. et al. Detection of phosphates originating from Enceladus’s ocean. _Nature_ 618, 489–493 (2023). Article  CAS  PubMed  PubMed Central  Google Scholar  * Waite, J. H.

Jr. et al. Cassini ion and neutral mass spectrometer: Enceladus plume composition and structure. _Science_ 311, 1419–1422 (2006). Article  CAS  PubMed  Google Scholar  * Rimmer, P. B. &

Shorttle, O. Origin of Life’s Building Blocks in Carbon- and Nitrogen-Rich Surface Hydrothermal Vents. _Life_ 9, 12 (2019). Article  CAS  PubMed  PubMed Central  Google Scholar  *

Capaccioni, B. et al. Light hydrocarbons in gas-emissions from volcanic areas and geothermal fields. _Geochem. J._ 27, 7–17 (1993). Article  Google Scholar  * Sanchez, R. A., Ferris, J. P.

& Orgel, L. E. Cyanoacetylene in Prebiotic Synthesis. _Science_ 154, 784–785 (1966). Article  CAS  PubMed  Google Scholar  * Schink, B. Fermentation of acetylene by an obligate

anaerobe,Pelobacter acetylenicus sp. nov. _Arch. Microbiol._ 142, 295–301 (1985). Article  CAS  Google Scholar  * Diender, M., Stams, A. J. M. & Sousa, D. Z. Pathways and Bioenergetics

of Anaerobic Carbon Monoxide Fermentation. _Front. Microbiol._ 6, 1275 (2015). Article  PubMed  PubMed Central  Google Scholar  * Wächtershäuser, G. Before enzymes and templates: theory of

surface metabolism. _Microbiol. Rev._ 52, 452–484 (1988). Article  PubMed  PubMed Central  Google Scholar  * Wächtershäuser, G. Evolution of the first metabolic cycles. _Proc. Natl Acad.

Sci._ 87, 200–204 (1990). Article  PubMed  PubMed Central  Google Scholar  * Huber, C. & Wächtershäuser, G. Activated acetic acid by carbon fixation on (Fe,Ni)S under primordial

conditions. _Science_ 276, 245–247 (1997). Article  CAS  PubMed  Google Scholar  * Diederich, P. et al. Formation, stabilization and fate of acetaldehyde and higher aldehydes in an

autonomously changing prebiotic system emerging from acetylene. _Commun. Chem._ 6, 38 (2023). Article  CAS  PubMed  PubMed Central  Google Scholar  * Sobotta, J. et al. A Possible Primordial

Acetyleno/Carboxydotrophic Core Metabolism. _Life_ 10, 35 (2020). Article  PubMed  PubMed Central  Google Scholar  * Seitz C., Eisenreich W. & Huber C. The Abiotic Formation of Pyrrole

under Volcanic, Hydrothermal Conditions—An Initial Step towards Life’s First Breath? _Life_ 11, 980 (2021). * de Duve C. Chapter 7 Harnessing Energy. In: _Blueprint for a cell: the nature

and origin of life_. (N. Patterson in 1991). * Frenkel-Pinter, M. et al. Thioesters provide a plausible prebiotic path to proto-peptides. _Nat. Commun._ 13, 2569 (2022). Article  CAS  PubMed

  PubMed Central  Google Scholar  * Closs, A. C., Bechtel, M. & Trapp, O. Dynamic Exchange of Substituents in a Prebiotic Organocatalyst: Initial Steps towards an Evolutionary System.

_Angew. Chem. Int. Ed._ 61, e202112563 (2022). Article  CAS  Google Scholar  * Geisberger, T., Sobotta, J., Eisenreich, W. & Huber, C. Formation of Thiophene under Simulated Volcanic

Hydrothermal Conditions on Earth—Implications for Early. _Life Extraterrest. Planets? Life_ 11, 149 (2021). CAS  PubMed  Google Scholar  * Giavalisco, P. et al. High-Resolution Direct

Infusion-Based Mass Spectrometry in Combination with Whole 13C Metabolome Isotope Labeling Allows Unambiguous Assignment of Chemical Sum Formulas. _Anal. Chem._ 80, 9417–9425 (2008). Article

  CAS  PubMed  Google Scholar  * Nieuwland, J. A., Calcott, W. S., Downing, F. B. & Carter, A. S. Acetylene polymers and their derivatives. I. The controlled polymerization of acetylene.

_J. Am. Chem. Soc._ 53, 4197–4202 (1931). Article  CAS  Google Scholar  * Kutscheroff, M. Ueber eine neue Methode direkter Addition von Wasser (Hydratation) an die Kohlenwasserstoffe der

Acetylenreihe. _Ber. der Dtsch. Chem. Ges._ 14, 1540–1542 (1881). Article  Google Scholar  * Jones, S. O. & Reid, E. E. The Addition of Sulfur, Hydrogen Sulfide and Mercaptans to

Unsaturated Hydrocarbons. _J. Am. Chem. Soc._ 60, 2452–2455 (1938). Article  CAS  Google Scholar  * Moritz, F. et al. The compositional space of exhaled breath condensate and its link to the

human breath volatilome. _J. Breath. Res._ 9, 027105 (2015). Article  PubMed  Google Scholar  * Ruf, A. & Danger, G. Network Analysis Reveals Spatial Clustering and Annotation of

Complex Chemical Spaces: Application to Astrochemistry. _Anal. Chem._ 94, 14135–14142 (2022). Article  CAS  PubMed  PubMed Central  Google Scholar  * Kohonen, T. Self-organized formation of

topologically correct feature maps. _Biol. Cybern._ 43, 59–69 (1982). Article  Google Scholar  * Weidner, L., Hemmler, D., Rychlik, M. & Schmitt-Kopplin, P. Real-Time Monitoring of

Miniaturized Thermal Food Processing by Advanced Mass Spectrometric Techniques. _Anal. Chem._ 95, 1694–1702 (2023). CAS  PubMed  Google Scholar  * Cronan J. E., Thomas J. Chapter 17

Bacterial Fatty Acid Synthesis and its Relationships with Polyketide Synthetic Pathways. In: _Methods in Enzymology_). (Academic Press, 2009). * Frenkel-Pinter, M., Sargon, A. B., Glass, J.

B., Hud, N. V. & Williams, L. D. Transition metals enhance prebiotic depsipeptide oligomerization reactions involving histidine. _RSC Adv._ 11, 3534–3538 (2021). Article  CAS  PubMed 

PubMed Central  Google Scholar  * Stubbs, R. T., Yadav, M., Krishnamurthy, R. & Springsteen, G. A plausible metal-free ancestral analogue of the Krebs cycle composed entirely of

α-ketoacids. _Nat. Chem._ 12, 1016–1022 (2020). Article  CAS  PubMed  PubMed Central  Google Scholar  * Pulletikurti, S., Yadav, M., Springsteen, G. & Krishnamurthy, R. Prebiotic

synthesis of α-amino acids and orotate from α-ketoacids potentiates transition to extant metabolic pathways. _Nat. Chem._ 14, 1142–1150 (2022). Article  CAS  PubMed  Google Scholar  * Yi, R.

et al. Alternating co-synthesis of glycol nucleic acid (GNA) monomers with dicarboxylic acids via drying. _Chem. Commun._ 59, 6865–6868 (2023). Article  CAS  Google Scholar  * Tziotis, D.,

Hertkorn, N. & Schmitt-Kopplin, P. Kendrick-Analogous Network Visualisation of Ion Cyclotron Resonance Fourier Transform Mass Spectra: Improved Options for the Assignment of Elemental

Compositions and the Classification of Organic Molecular Complexity. _Eur. J. Mass Spectrom._ 17, 415–421 (2011). Article  CAS  Google Scholar  Download references ACKNOWLEDGEMENTS This

research was funded by the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) – Project-ID 364653263 – TRR 235 (CRC 235). C.S. and C.H. thank the Hans-Fischer-Gesellschaft

(D-Munich) for financial support. Furthermore, this project was funded by the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) under Germany´s Excellence Strategy - EXC 2094

- 390783311 (A.R.). FUNDING Open Access funding enabled and organized by Projekt DEAL. AUTHOR INFORMATION AUTHORS AND AFFILIATIONS * Helmholtz Munich, Research Unit Analytical

BioGeoChemistry, Neuherberg, Germany Philippe Diederich, Leopold Weidner & Philippe Schmitt-Kopplin * Excellence Cluster ORIGINS, Boltzmannstraße 2, 85748, Garching, Germany Alexander

Ruf * LMU Munich, Faculty of Physics, Schellingstraße 4, 80799, Munich, Germany Alexander Ruf * Technical University of Munich, TUM School of Natural Sciences, Department of Bioscience,

Bavarian NMR Center (BNMRZ), Structural Membrane Biochemistry, Lichtenbergstr. 4, 85748, Garching, Germany Thomas Geisberger, Christian Seitz, Wolfgang Eisenreich & Claudia Huber *

Comprehensive Foodomics Platform, Chair of Analytical Food Chemistry, TUM School of Life Sciences, Technical University of Munich, Maximus-von-Imhof-Forum 2, 85354, Freising, Germany Leopold

Weidner & Philippe Schmitt-Kopplin * Center for Astrochemical Studies, Max Planck Institute for Extraterrestrial Physics, Gießebachstraße 1, 85748, Garching bei München, Germany

Philippe Schmitt-Kopplin Authors * Philippe Diederich View author publications You can also search for this author inPubMed Google Scholar * Alexander Ruf View author publications You can

also search for this author inPubMed Google Scholar * Thomas Geisberger View author publications You can also search for this author inPubMed Google Scholar * Leopold Weidner View author

publications You can also search for this author inPubMed Google Scholar * Christian Seitz View author publications You can also search for this author inPubMed Google Scholar * Wolfgang

Eisenreich View author publications You can also search for this author inPubMed Google Scholar * Claudia Huber View author publications You can also search for this author inPubMed Google

Scholar * Philippe Schmitt-Kopplin View author publications You can also search for this author inPubMed Google Scholar CONTRIBUTIONS P.D. conceived and designed the analysis, collected the

data, performed experiments, performed data analysis, and wrote the paper. A.R., L.W., T.G., C.S., and C.H. contributed analysis tools. T.G. and C.S. performed experiments. C.H., W.E.,

P.S.K., A.R., and L.W. edited the paper. P.S.K., C.H., and W.E. provided funding, supervised the project, and edited the paper. CORRESPONDING AUTHORS Correspondence to Claudia Huber or

Philippe Schmitt-Kopplin. ETHICS DECLARATIONS COMPETING INTERESTS The authors declare no competing interests. PEER REVIEW PEER REVIEW INFORMATION _Communications Chemistry_ thanks Malak

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ARTICLE Diederich, P., Ruf, A., Geisberger, T. _et al._ C2-addition patterns emerging from acetylene and nickel sulfide in simulated prebiotic hydrothermal conditions. _Commun Chem_ 6, 220

(2023). https://doi.org/10.1038/s42004-023-01021-1 Download citation * Received: 18 July 2023 * Accepted: 03 October 2023 * Published: 12 October 2023 * DOI:

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