Allophycocyanin A is a carbon dioxide receptor in the cyanobacterial phycobilisome

Light harvesting is fundamental for production of ATP and reducing equivalents for CO2 fixation during photosynthesis. However, electronic energy transfer (EET) through a photosystem can harm the photosynthetic apparatus when not balanced with CO2. Here, we show that CO2 binding to the light-harvesting complex modulates EET in photosynthetic cyanobacteria. More specifically, CO2 binding to the allophycocyanin alpha subunit of the light-harvesting complex regulates EET and its fluorescence quantum yield in the cyanobacterium Synechocystis sp. PCC 6803. CO2 binding decreases the inter-chromophore distance in the allophycocyanin trimer. The result is enhanced EET in vitro and in live cells. Our work identifies a direct target for CO2 in the cyanobacterial light-harvesting apparatus and provides insights into photosynthesis regulation.

Light harvesting is fundamental for production of ATP and reducing equivalents for CO 2 fixation during photosynthesis. However, electronic energy transfer (EET) through a photosystem can harm the photosynthetic apparatus when not balanced with CO 2 . Here, we show that CO 2 binding to the lightharvesting complex modulates EET in photosynthetic cyanobacteria. More specifically, CO 2 binding to the allophycocyanin alpha subunit of the lightharvesting complex regulates EET and its fluorescence quantum yield in the cyanobacterium Synechocystis sp. PCC 6803. CO 2 binding decreases the interchromophore distance in the allophycocyanin trimer. The result is enhanced EET in vitro and in live cells. Our work identifies a direct target for CO 2 in the cyanobacterial light-harvesting apparatus and provides insights into photosynthesis regulation.
Oxygenic photosynthesis evolved in the cyanobacteria about 2.5 Gyr ago and provided much of our current atmospheric O 2 1 . Cyanobacteria gather photons using a harvesting antenna known as the phycobilisome (PBS). Phycobiliproteins (PBPs) constitute PBSs to produce one of the largest protein complexes known. The PBPs include phycocyanin, phycoerythrin and allophycocyanin, together with their associated linker proteins 2 . PBS light absorption is achieved by open-chain tetrapyrrole (bilin) chromophores covalently attached to the PBPs and their associated linker proteins 3 . Two subunits of a PBP, an αand a βsubunit, form an αβ heterodimer known as an (αβ) monomer, which is assembled into an (αβ) 3 trimer. Electronic energy transfer (EET) within the (αβ) 3 trimer is fast and efficient (on the sub-ps to ps timescales) 4 . The PBP (αβ) 3 trimers form the ordered supramolecular lightharvesting complex via the linker proteins 5 . A typical cyanobacterial hemidiscoidal PBS consists of a central core surrounded by peripheral chromophore-containing rods that capture photons 6 . The PBS core transfers excitation energy via a terminal emitter to the photosynthetic reaction centres with the subsequent synthesis of ATP and NADPH 7 . CO 2 assimilation into sugars requires NADPH and ATP. There is evidence from non-cyanobacterial model systems that CO 2 fixation and availability are coupled to light-harvesting 8,9 . For example, CO 2deficient conditions in algae reduce photosystem (PS) II antenna size, and PSI/PSII fluorescence intensity increases 10,11 . A light-harvesting chlorophyll-protein complex II migrated from PSII to PSI under CO 2deficient conditions in Chlamydomonas 12 . Insufficient CO 2 can also result in over-reduction of the plastoquinone pool, resulting in singlet oxygen species and photoinhibition 13 . The addition of a suitable carbon source under CO 2 -deficient conditions restored photosynthetic activity 14 .
The mechanism(s) that couples inorganic carbon availability to light-harvesting is uncertain. In higher plants, bicarbonate binding to PSII 15 . However, questions remain as HCO 3 − is also proposed to be tightly bound to PSII under physiologically relevant environmental CO 2 , meaning this binding site's role as an authentic regulatory site at limiting CO 2 awaits further experimentation 16 . Nevertheless, there is considerable evidence that CO 2 /HCO 3 − availability can regulate lightharvesting and subsequent EET.
How might CO 2 regulate light-harvesting? CO 2 and protein can interact through carbamates on neutral N-terminal α-aminoor lysine ε-amino groups. For example, carbamylation regulates the activities of Rubisco 17 , haemoglobin (Hb) 18 , and ubiquitin 19 . In addition, several proteins carry a stable carbamate required for catalysis, e.g., urease, alanine racemase, transcarboxylase 5 S, class D β-lactamase and phosphotriesterase 20 . Therefore, we and others have hypothesized that reversible carbamylation of neutral N-terminal α-amino groups and/or lysine ε-amino groups could form a widespread mechanism for protein regulation by CO 2 17,20 . We developed triethyloxonium tetrafluoroborate (TEO) as a chemical proteomics tool to identify carbamate post-translational modifications (PTMs) 20 . We hypothesised the TEO chemical proteomics tool could be used to discover CO 2 -binding proteins in the cyanobacterial PBS to determine the mechanistic basis for coupling CO 2 availability to EET. Here we describe the discovery of a CO 2 -binding site in the PBS and its role in regulating EET.

Synechocystis sp. PCC 6803 allophycocyanin A binds CO 2
An extract of Synechocystis sp. PCC 6803 soluble protein was incubated with 20 mM NaH 14 CO 3 and subjected to TEO-trapping (Fig. 1a). An insignificant level of 14 CO 2 was incorporated into the protein extract in the absence of TEO. The inability to observe protein-bound 14 CO 2 in the absence of TEO is likely due to the ready reversibility of carbamylation that leads to sample degassing during preparation for analysis. However, the TEO-trapped protein lysate contained significant protein-bound 14 CO 2 , even when accounting for 50% of the total protein sample being Rubisco. Thus, we conclude that the Synechocystis proteome contains CO 2 -interacting proteins carbamylated at labile sites exchangeable with the environment. We proceeded to identify carbamate PTMs to investigate proteins that couple CO 2 Table 1). The MSMS spectrum lacked detectable b ions crossing the modification. Therefore, independent experiments were performed and identified the same carbamylation site with either both y and b ions or only b ions crossing the modification (Supplementary Fig. 2; Supplementary Table 2). In all cases, the K6 carbamate was identified on the internal lysine residue of the peptide, a so-called missed cleavage. Carbamylation removes the positive charge on the lysine that is essential for cleavage site recognition by trypsin. This missed cleavage supports the Slr2067 K6 carbamate as genuine as a missed cleavage is an otherwise rare event, despite the suboptimal spectra quality. The slr2067 gene encodes the allophycocyanin α-subunit (ApcA). ApcA is the α-subunit of the allophycocyanin (αβ) 3 trimer located within the PBS core. It has a critical role in EET from the PBS antennal proteins to the photosystem via the terminal pigment. We identified the same carbamate PTM on ApcA residue K6 in TEOtrapping experiments performed on isolated PBS ( Fig. 1c; Supplementary Table 3) and purified recombinant ApcAB (αβ) 3 trimer ( Fig. 1d; Supplementary Fig. 3). We performed the CO 2 trapping experiments on ApcA with 13 CO 2 to corroborate the carbamate PTM by interrogating the MS/MS data for a 73.0211 Da modification. The expected +1 Da m/z increase (from 72.0211 Da) was observed for the carbamylation site at K6 (Fig. 1e). We performed a control experiment to identify the reason for the relative difficulty in observing multiple ions that encompass the K6 carbamate. Synthetic SIVTKSIVNADAEAR peptide was equilibrated with 50 mM CO 2 /HCO 3 − at pH 8.5, TEO was added, and the peptide analysed by MS/MS (Supplementary Fig. 4; Supplementary Tables 4-6) 20 . MS/MS fragment ions that cross K6 were observed to be lower intensity for the carboxyethylated peptide compared to the unmodified or ethylated peptide (note how the intensity of the labelled ions is almost indistinguishable from background non-specific ions in Supplementary Fig. 4b compared to Supplementary Fig. 4a, c). Therefore, the relative difficulty of observing the carbamate modification on K6 by LC-MS/MS is an intrinsic property of the carboxyethylated peptide.
To compensate for the relative difficulty in using MS/MS to observe a carbamate at K6, we used 13 C-NMR as an orthologous method to confirm the ApcA CO 2 -binding site at K6. Carbamate formation on wild type recombinant ApcA (αβ) 3 trimer (ApcAB WT (αβ) 3 ) was confirmed using 13 C-NMR spectroscopy by observing a signal at 165 ppm, which matched literature values for carbamate formation (Fig. 1f) 21 . We generated a K6A mutant recombinant protein (ApcAB K6A (αβ) 3 ) to investigate whether the observed 13 C-NMR signal was due to the carbamate forming at K6. We also generated a K6E mutant recombinant protein (ApcAB K6E (αβ) 3 ) as we hypothesised that mutation of K6 to glutamate would represent the local carbamate charge state at 100% occupancy. Circular dichroism spectra for ApcAB WT (αβ) 3 versus ApcAB K6A (αβ) 3 and ApcAB K6E proteins demonstrated that the three proteins possessed similar secondary structures ( Supplementary  Fig. 5). Therefore, there is no gross alteration in the ApcAB K6A (αβ) 3 structure in the mutant protein.
No signal corresponding to a carbamate was observed in ApcAB K6A (αβ) 3 trimers. ApcA is, consequently, a CO 2 -binding protein via carbamylation of K6 at photosynthetically appropriate gas levels 22 .
Carbamylated ApcA peptide detection was not sufficiently reliable to quantify carbamylation at varying CO 2 /HCO 3 − by either labelling or label-free methods and 13 C-NMR was insufficiently sensitive. However, we hypothesised that increased ApcA carbamylation could be indirectly monitored through a decreased observation of the unmodified peptide. ApcAB WT (αβ) 3 was equilibrated with varying CO 2 /HCO 3 − at pH 7.4, TEO was added to trap carbamate PTMs, and samples were analysed by ESI-MS/MS. However, the unmodified K6-containing peptide was more reliably detected by MS/MS than the modified peptide. Therefore, we measured the peak area of the unmodified K6containing peptide and calculated it as a ratio of the peak area of four other control peptides. At varying CO 2 /HCO 3 − , this ratio was compared to the absence of CO 2 /HCO 3 − (Supplementary Fig. 6). The control peptides were also compared to one another. CO 2 /HCO 3 − caused an immediate decrease in the relative amount of the unmodified peptide, which we infer is due to an increase in the modified peptide. This decrease did not occur for the control peptides. The equivalent drop in the K6-containing peptide at all [CO 2 /HCO 3 − ] suggested that the carbamate might be acting as an on/off switch in the presence or absence of CO 2 .

CO 2 alters allophycocyanin A inter-chromophore distance
We used molecular dynamics (MD) simulations to understand the mechanism underlying the increase in QY in ApcAB WT (αβ) 3 trimer. To this end, we performed two 1 μs simulations of Thermosynechococcus vulcanus (PDB: 3DBJ; ref. 25) ApcAB WT (αβ) 3 trimer (apo and CO 2 bound). The ApcAB (αβ) 3 trimer has six chromophore-binding pockets that we defined as either monomeric (enclosed by residues of a monomer alone) or interface (enclosed by residues of adjacent monomers) (Fig. 3a). Analysis of the root mean square deviation (RMSD) with reference to the initial state demonstrated that both simulations stabilised after 600 ns ( Supplementary Fig. 9). We examined the rotamer states for K6, whether apo or CO 2 -bound (Supplementary Fig. 10, Supplementary Table 8). We observed an overall change in the occupancy of rotamer states and noted the loss of a major rotamer when CO 2 -bound corresponding to χ 1~7 5°. Contact analysis demonstrated the disruption of a salt bridge between K6 and D100 in the CO 2 -bound state (Fig. 3b, Supplementary Fig. 11) where D100 resides on an α-helix that couples K6 to the chromophorebinding site. Two helices in the (αβ) 3 trimer showed a higher RMSD in the CO 2 -bound state ( Supplementary Fig. 12). This higher RMSD reflected a change in the contact frequency between the chromophore and binding-pocket residues for both the monomer ( Supplementary  Fig. 13a) and interface ( Supplementary Fig. 13b) pockets as observed during the last equilibrated 300 ns of the simulations.
We asked whether the alterations in (αβ) 3 trimer contact frequency could result in changes that explained the difference in QY with CO 2 /HCO 3 − . Therefore, we measured the change in distance of each chromophore pair (i.e., one chromophore bound to an interface pocket of an αβ heterodimer and one bound to a monomer pocket of another heterodimer) (Fig. 3c, d). We observed that in the last 300 ns of the simulation, distances are comparable between all three chromophore pairs (24-25 Å) without CO 2 (Fig. 3c), but the distance of one pair reduces to 22 Å when CO 2 -bound (Fig. 3d). Therefore, the implication is that the reduced inter-chromophore separation enhances EET to the final emitting site in the system. These data would accordingly support the observations of the basal fluorescent QY for ApcAB WT , ApcAB K6A , ApcAB K6E (αβ) 3 trimers (Fig. 2c). ApcAB K6E resembles a fully carbamylated ApcAB protein and thus shows the most significant increase in QY. The ApcAB K6A protein also has an ablated salt-bridge between K6 and D100, so basal QY is increased relative to ApcAB WT but not as much as ApcAB K6E presumably because the new contacts made by the anionic carbamate are not present.
The monomer-and interface-pocket chromophores have been proposed to form exciton-coupled pairs in (αβ) 3 trimers 26 . However, a weaker coupling regime allowing for incoherent EET according to the Förster mechanism has also been proposed 4,24 . When two chromophores with similar excitation energies are located close to one another and chirally disposed, the excited state can delocalise over both chromophores to become an exciton. Exciton interactions are important in photosynthetic light-harvesting complexes by expanding the spectral cross-section to permit faster and more robust EET 27 . However, in a weaker coupling regime, EET, according to the Förster mechanism, is applicable, and the rate of EET can be obtained for a given pairwise interaction and separation. The rate of Förster EET is provided by Where R of and R DA is the Förster radius and distance in the donoracceptor pair, respectively. κ 2 is a mutual orientation factor, and τ D is the donor fluorescence lifetime. Using a Förster radius of 68.0 Å 23 , a fluorescence lifetime of 1.5 ns 24 , and a mutual orientation factor of 1.0, we obtain an EET time of 3.3 ps for a distance of 24.5 Å (without CO 2 ) and 1.7 ps for a distance of 22.0 Å (in the presence of CO 2 ). These values are similar to previously measured EET rates in related systems 4,24 . The orientation factor κ 2 has a range; 0 ≤ κ 2 ≤ 4. For κ 2 = 1.0 the interaction dipoles adopt a "sandwich" configuration. If the orientation factor substantially impacted the rate of electronic energy transfer on CO 2 binding, there would have to be a change in mutual dipole orientation from the "sandwich" towards an "in line" configuration. No structural change consistent with this configuration change was evidenced from the molecular dynamics simulations. Therefore, altered change in distance between interacting chromophores is the significant contributor to the modulation of the electronic energy transfer. The increased EET rate calculated from distances measured in our MD simulations correlates with the higher QY measured for ApcAB (αβ) 3 trimers in the presence of CO 2 and corroborates our hypothesis.
We employed ultrafast transient absorption spectroscopy to validate the calculated EET rates experimentally. The ApcAB (αβ) 3 trimers of Synechococcus sp. PCC 7002 used for in vitro biochemistry are very similar in structure to the ApcAB (αβ) 3 trimers of Thermosynechococcus vulcanus used for molecular dynamics ( Supplementary  Fig. 14). Synechoccus ApcAB (αβ) 3 trimers were, therefore, used for ultrafast transient absorption spectroscopy. ApcAB (αβ) 3 trimers were monitored over a 2.5 ps time window after excitation by a~200 fs optical pulse at 515 nm (Fig. 4, Supplementary Fig. 15). Probing the absorption recovery at 610-630 nm revealed a fast initial stimulated emission component of 200-400 fs, observed in both the absence and presence of CO 2 in both ApcAB WT (αβ) 3 and ApcAB K6A (αβ) 3 trimers. We attribute this fast initial stimulated emission component to relaxation within the strongly coupled αβ dimer, consistent with earlier work 28 . PCC 7002 ApcAB WT (αβ) 3 , ApcAB K6A (αβ) 3 , or ApcAB K6E (αβ) 3 trimers (*p = 0.0036, one sample t-test, ratio is derived from n = 11 independent replicates for WT and n = 7 independent replicates for K6A, mean ± 95% CI). The 200-400 fs component is followed by a stimulated emission component in the ps timescale (the EET rate according to the Förster mechanism) which is modulated by CO 2 in ApcAB WT (αβ) 3 . In the absence of CO 2 , we observed a long lifetime component significantly longer than could be fit with the period of data acquisition. The lifetime was significantly reduced in the presence of CO 2 and could be fit to give a value of 2.9 ps (τ 1 = 200 fs (60% of the amplitude), τ 2 = 2.9 ps (40% of the amplitude)). Crucially, in ApcAB K6A (αβ) 3, the stimulated emission component was too long to be fit by the data and was also not observed to be reduced by CO 2 within the sensitivity of the experiment. We conclude that this stimulated emission component is due to weaker coupling Förster EET within ApcAB (αβ) 3 . The modulation of this component with CO 2 is consistent with the distance variations predicted in the MD simulations. Further, the Förster EET rates measured here are on a ps timescale and therefore compatible with the values calculated from MD simulations. In conclusion, ultrafast transient absorption measurements show an enhanced rate of Förster EET in ApcAB WT (αβ) 3 in the presence of CO 2 . Consequently, we propose that the CO 2 enhanced EET rate reduces the yield of non-radiative decay early in the allophycocyanin EET sequence. Thus, the excitation energy is more effectively transferred to the final emitting state, resulting in a higher fluorescence QY.

Allophycocyanin A CO 2 -binding regulates EET in the cell
We next assessed whether CO 2 /HCO 3 − enhanced EET in the context of the whole organism. QY measurements from the PBS in vivo are typically an order of magnitude lower than for the isolated recombinant proteins. This decreased QY is due to efficient EET from the PBS to the photosystem via the terminal pigment and subsequent photochemistry (charge separation and electron transfer) at the reaction ApcA is shown in red and ApcB in blue. b K6 forms a salt bridge with D100. D100 is sited on an α-helix that connects to the chromophore-binding pocket. c Plot of the frequency of distance against inter-chromophore distance for three monomerinterface chromophore pairs in the apo state. d Plot of the frequency of distance against inter-chromophore distance for three monomer-interface chromophore pairs in the CO 2 -bound state. Source data are provided as a Source Data file.
centres. Therefore, the observed QY in vivo reflects energy lost from the PBS that is not transmitted to the photosystem. However, we reasoned that an increased observed QY would be reflective of increased EET to the photosystem due to reduced non-radiative decay at the initially excited chromophores, as previously discussed.
We used CRISPR-Cpf1 to generate Synechocystis sp. PCC 6803 with single amino acid mutations at K6 in ApcA. Absorption spectra were measured for wild type, K6A and K6E cells and were broadly similar ( Supplementary Fig. 16). The relative peak heights for the PBS were similar in all strains ( Supplementary Fig. 16 inset). The peak height for P680 for K6E cells was increased. As this absorption at the photosynthetic reaction centre is downstream of the effects studies at the PBS, this strain was still investigated further. We depleted Synechocystis sp. PCC 6803 wild type and K6A cells of CO 2 /HCO 3 − under cool white light and measured the fluorescence QY when exciting chlorophyll a and PBS at 485 nm and measuring emission at 660 nm (Fig. 5a). Although 485 nm will also excite carotenoids, their low QY and efficient electronic energy transfer to chromophores makes it very unlikely they will impact on the observations. We observed a slight but significant enhancement of QY for wild type cells but not K6A cells when exposed to CO 2 /HCO 3 − . The observed effect is small, as expected, as energy transfer from the PBS to the photosystem is extremely efficient. However, both the small size of the effect and the indirect measure of EET limited the utility of this approach. We, therefore, measured whole-cell fluorescence lifetimes at 660 nm for wild type, K6A and K6E cells excited at 635 nm (Table 1; Fig. 5b). Two predominant fluorescent lifetimes on the ps timescale were observed. No difference in lifetime or fluorescence amplitude was observed between cells in the presence of NaCl or CO 2 /HCO 3 − within the measurement error for the experiment. However, the τ 2 fluorescence lifetime for both K6A and K6E cells was significantly longer than for wild type cells, indicating increased energy transfer to the emitting species (Fig. 4b). This observation is consistent with the increased basal fluorescent QY for ApcAB K6A , ApcAB K6E (αβ) 3 trimers compared to wild type (Fig. 2c) and decreased inter-chromophore distance (Fig. 3d). The 635 nm excitation wavelength can also excite phycocyanin. However, as the effect on the τ 2 fluorescence lifetime is dependent on allophyocyanin genotype (Table 1), the impact of phycocyanin is likely minimal but cannot be ruled out.
Together, the data support the hypothesis that carbamate formation at ApcA K6 breaks a salt bridge with D100 and enhances EET in whole cells.

Discussion
The Calvin-Benson-Bassham (CBB) cycle rate depends on multiple factors. However, PCO 2 is particularly important as it determines the relative rate of RuBisCO carboxylation compared to the competing oxygenation reaction. Following ribulose-1,5-biphosphate carboxylation, the CBB cycle requires ATP and NADPH, whose availability is controlled by light-dependent reactions. Therefore, although the lightdependent reactions might be independent of substrate availability, reduced PCO 2 could represent a bottleneck for the ensuing lightindependent reactions. It follows that an organism should optimise the light-dependent reaction rate to fit the changing environmental conditions that, under specific adverse scenarios, could lead to damage of the photosystems. Therefore, it seems paramount that CO 2 can have a regulatory effect at the level of light-harvesting and/or lightdependent reactions for 'sink to source' regulation. The finding of a CO 2 -mediated PTM in the PBS might represent such a mechanism.

CO 2 trapping
All CO 2 trapping experiments were conducted in phosphate buffer (4 mL, 50 mM, pH 7.4). The solution was transferred to a potentiometric titrator (902 Titrando; Metrohm) and incubated at 25°C with stirring. Next, a freshly made solution of triethyloxonium tetrafluoroborate (Et 3 OBF 4 ; (280 mg, 1.47 mmol) in dH 2 O (1 mL)) was added stepwise with a constant pH maintained (pH 7.4) through the slow addition of 1 M NaOH solution via the automatic burette. The reaction mixture was stirred, and the pH was maintained for 1 h after the final Et 3 OBF 4 addition to ensure that all TEO was hydrolysed. The reaction mixture was then dialysed against dH 2 O (1 L) overnight.

Mass spectrometry
The post-dialysis reaction trapping sample supernatant was removed using vacuum centrifugation. The dried protein sample was resuspended in 8 M urea and reduced with dithiothreitol (DTT, 25 mM final concentration) at 37°C for 1 h. The sample was then alkylated with iodoacetamide (40 mM final concentration) in the dark for 1 h. This sample was then centrifuged at 1000 g for 5 min and the soluble supernatant removed. The sample was diluted to 1 M urea and digested with trypsin gold (mass spectrometry grade, Promega) in a 1:25 (w/w) ratio overnight at 37°C. The digested solution was then desalted on a C18 column and analysed by ESI-MS/MS on an LTQ Orbitrap XL mass spectrometer (Thermo) coupled to an Ultimate 3000 nano-HPLC instrument. Peptides eluted from the LC gradient were injected online to the mass spectrometer (lock mass enabled, mass range 400-1800 Da, resolution 60,000 at 400 Da, 10 MS/MS spectra per cycle, collision-induced dissociation (CID) at 35% normalised CE, rejection of singly charged ions). The post-run raw data files were converted into.mgf files using the freeware MSConvert provided by Proteowizard 29 . mgf files were analysed using PEAKS Studio 10.5 software 30 , including the variable modifications ethylation (28.03 at D or E), carboxyethylation (72.02 at K or protein N-terminal groups), oxidation (M), acetylation (N-terminal) and the fixed modification carbimidomethyl (C). These data were then refined using a false discovery rate of 1%, two unique peptides per protein and a PTM AScore of 50. Three carbamates PTMs were discovered (including on ApcA). The two additional carbamate PTMs will be reported elsewhere.

NMR
Recombinant allophycocyanin alpha subunit wild type and K6A mutant protein were prepared in phosphate saline buffer, pH 7.4, 50 mM NaH 13 CO 3 with 20-50% D 2 O. 13 C-NMR experiments spectra were acquired with a Varian 600 MHz spectrometer equipped with an Agilent OneNMR Probe to deliver a maximum pulsed-field gradient strength of 62 G cm −1 . A 1 H spectrum was acquired to examine for small molecule impurities. Thirteen 1 H experiments were recorded in 12 h, collecting 131072 complex points. The repetition time was 6.7 s, of which 1.7 s comprised the acquisition time. The excitation pulse angle was set to 45 degrees. The strong interfering H 2 O signal was eliminated using the Robust-5 pulse sequence 31 . Thirty-two 13 C scans were collected, comprising 65 536 complex data points and a spectral width of 10 kHz. The repetition time was 6.3 s, of which 3.3 s comprised the acquisition time. The W5 inter-pulse delay was set to 240 µs. Rectangular 1 ms pulsed-field gradients were used in all cases with a strength of G1 = 28.3 G cm −1 (first pair) and G2 = 4.9 G cm −1 (second pair). The gradient stabilisation delay was 0.5 ms. The first pair of lock prefocusing field gradients were separated from the first radio-frequency pulse by a 1.5 ms delay.

Cyanobacterial genetic manipulation
Synechocystis sp. PCC 6803 was cultivated in a BG-11 liquid medium with a pH of 8.0 at 28°C. Phycobilisome isolation was performed according to the method of ref. 32. The plasmid pSL2680 containing cpf1, the native Francisella novicida CRISPR array and LacZ, amplified from the pCrispomyces-2, served as the base plasmid for construction of slr2067 K6 editing plasmids 33 . pSL2680 expressing full-length pre-crRNAs was constructed by cloning annealed oligonucleotides (5′-AGA TAT TTC GTG ACG ATA CTC ATG G-3′ and 5′-AGA CCC ATG AGT ATC GTC ACG AAA T-3′) into the AarI sites to yield pSL2680apcAgRNA. PCR was used to synthesise the homology regions which were cloned into the KpnI site on the plasmids containing the matching crRNA. The point mutation homology region was constructed in two pieces using oligonucleotides 5′-CAT TTT TTT GTC TAG CTT TAA TGC GGT AGT  TGG TAC CCT TTA ATA AGC TTG   ) or NaCl for Synechocystis sp. PCC 6803 wild type or K6A cells (*q = 0.0058, one-way ANOVA with post hoc two-stage linear set-up procedure of Benjamini, Krieger and Yekutieli, n = 6 independent replicates for WT + NaCl, K6A + NaCl and K6A + CO 2 , n = 5 independent replicates for WT + CO 2 , t = 2.382, df = 19, nd no discovery, mean ± 95% CI). b The second fluorescent lifetime component (Table 1) with 1 mM NaHCO 3 (-CO 2 ) or NaCl (-Na) for Synechocystis sp. PCC 6803 wild type, K6A, or K6E cells (*p < 0.05, ns = not significant, two-way ANOVA of data from Table 1 with post hoc Tukey test, n = 6 independent replicates, mean ± 95% CI). Source data are provided as a Source Data file.  and 5′-GCC CGG ATT ACA GAT CCT CTA GAG TCG ACG GTA CCG GCT CAC CTG TGA TGC CAT TG-3′/5′-CCA TGA GTA TCG TCA CGG CAT  CGA TCG TGA ATG CTG ATG CAG AAG C-3′ for the K6A mutation and  5′-CAT TTT TTT GTC TAG CTT TAA TGC GGT AGT TGG TAC CCT TTA  ATA AGC TTG GGT ACA CAG AC-3′/ 5′-GCT TCT GCA TCA GCA TTC  ACG ATC GAT TCC GTG ACG ATA CTC ATG G-3′ and 5′-GCC CGG ATT  ACA GAT CCT CTA GAG TCG ACG GTA CCG GCT CAC CTG TGA TGC  CAT TG-3′/5′-CC ATG AGT ATC GTC ACG GAA TCG ATC GTG AAT GCT GAT GCA GAA GC-3′ for the K6E mutation. The homology templates were assembled, linearised with KpnI, and PCR was used to generate pSL2680-K6AapcA and pSL2680-K6EapcA. E. coli with cargo plasmid either pSL2680-K6AapcA or pSL2680-K6EapcA and E. coli with conjugal plasmid pRL443 were grown overnight at 37°C. 10 mL of each culture was pelleted and resuspended in 10 mL LB media without antibiotics. Cargo and conjugal cultures were mixed and 200 µl combined with 100 µl of Synechocystis culture. The mixture was incubated for 5 h at 30°C before plating on BG11 agar plates without antibiotics. Plates were incubated for 2 days at 30°C. 15 μg mL −1 kanamycin was added, and plates were incubated at 30°C with light for 10 days until colonies appeared. At least four rounds of streak purification were performed to ensure complete segregation. Colonies were cured of plasmids on BG11 agar without antibiotics. Two mutant strains were produced for each point mutation.
Cyanobacterial manipulation for spectroscopy  Fig. 1b). The ApcAB protein from Synechococcus sp. PCC 7002 can be produced as a recombinant in Escherichia coli as a recombinant protein and was, therefore, used for in vitro biochemistry. Expression plasmid carrying Synechococcus sp. PCC 7002 ApcAB were cotransformed into E. coli BL21(DE3) cells with plasmids for chromophorylation. A 50-ml starter culture was added to 1 L of LB medium with the appropriate combination of antibiotics and shaken at 37°C for 4 h until the optical density at 600 nm (OD600) was 0.6. Recombinant protein production was induced by addition of 0.5 mM isopropyl-γ-D-thiogalactoside (IPTG). Cells were incubated with shaking at 30°C for another 4 h before they were harvested by centrifugation at 10,000 × g. Cells containing recombinant protein were thawed and resuspended in buffer O (50 mM Tris-HCl, 150 mM NaCl; pH 8.0) at 1 g (wet weight) cells/2.5 ml and then were lysed by French Press. The lysed cell suspension was centrifuged at 13,000 × g, and the recombinant protein purified using a nickel-nitrilotriacetic acid column 34 . Plasmid construction for production of recombinant Synechococcus sp. PCC 7002 ApcAB mutant plasmid was performed using standard molecular techniques and mutagenic primers 5′-ATG AGT ATT GTC ACG GCA TCC ATC GTG AAT GCC GAC-3′ and 5′-GTC GGC ATT CAC GAT GGA TGC CGT GAC AAT ACT CAT-3′ for K6A and 5′-GTC ACG GAA TCC ATC GTG AAT GCC GAC GCT G-3′ and 5′-GAT GGA TTC CGT GAC AAT ACT CAT GGT GAA GGG ATG-3′ for K6E.

Molecular Dynamics simulations
Comparing the structures of (αβ) 3 36 , shows that they are very similar (Supplementary Fig. 13). Accordingly, structural superpositions provided low RMSD values between the (αβ) 3 trimers; 0.78 Å RMSD between trimers from 3DBJ and 4PO5, 1.56 Å RMSD between trimers from 3DBJ and 7EXT, and 1.82 Å RMSD between trimers from 4PO5 and 7EXT. All-atom molecular dynamics simulations of Thermosynechococcus vulcanus (PDB: 3DBJ [https://www.rcsb.org/ structure/3DBJ]) ApcAB (αβ) 3 trimer in its apo and CO2-bound form were carried out using the AMBER18 molecular modelling software 37 . The topology and the initial coordinate files were generated using the LEaP module of AmberTools18. The systems simulated features no histidine, all other titratable groups were assigned to their default protonation state at 7.4 pH. The ff14SB 38 version of the all-atom Amber force field was used to represent the protein systems. The parameters for chromophore and non-standard amino acid residues (N-methyl asparagine and CO 2 -bound lysine) were taken from the GAFF2 forcefield 39 , and the missing ones were generated with Antechamber 40 (see Supplementary Data file). Each system was solvated with an explicit TIP3P water model and neutralised with the required number of randomly placed K + /Cl − ions. The ion count was adjusted to account for an osmolarity of 0.15 M.
The systems were independently subjected to 2-step energy minimisation with a combination of steepest descent and conjugate gradient methods using the pmemd programme implemented in AMBER to relax internal constraints by gradually releasing positional restraints. The first minimisation step had positional restraints on protein backbone atoms (Cα, C, N) and the chromophore with a restraint force constant of 10.0 kcal/mol/Å 2 , which were then removed in the second minimisation step. Following this, the systems were gradually heated to 300 K under constant volume (NVT) for 500 ps with positional restraints (restraint force constant of 5.0 kcal/mol/Å 2 ) on the protein Cα atoms and the entire ligand. They were then density equilibrated for 5 ns under constant pressure (NPT) to bring the atmospheric pressure of the system to 1 bar. Microsecond long production run was performed for each system under NPT conditions. Langevin thermostat (collision frequency of 1 ps −1 ) was used to maintain a constant temperature and Berendsen barostat for pressure scaling. An integration time step of 2 fs was used, with all bonds to hydrogen atoms constrained with the SHAKE algorithm. The particlemesh Ewald (PME) algorithm was used to evaluate long-range electrostatic forces with a non-bonded cut-off of 9 Å. Coordinates were saved every 10 ps. MD trajectories were analysed using the cpptraj module of AmberTools18 and VMD1.9.2 41 .

Steady-state absorption and fluorescence spectroscopy
Absorption spectra and fluorescence spectra were obtained using a Synergy H4 Plate Reader and/or a Cary 5000 UV-Vis-NIR. Steady-state fluorescence was measured using a Jobin Yvon Horiba Fluorlog 3. Photoluminescence quantum yield measurements on solutions were carried out according to the absolute method, using an integrating sphere. The optical density of recombinant proteins was adjusted to 0.1 at their fluorescence maximum. For in vitro PLQY measurements using recombinant protein, measurements were made before and after the addition of 20 mM CO 2 /HCO 3 − or NaCl to calculate the impact of the addition. Data is presented at the ratio of PLQYs with CO 2 /HCO 3 − or NaCl.

Circular dichroism
Spectra were collected in high transparency quartz cuvettes with a 0.1 cm path length using a Jasco J-1500 spectropolarimeter equipped with a mini-circulation bath and Peltier stage. Spectra for secondary structure determination were measured from 190-260 nm in PBS, pH 7.4, at a protein concentration of 12.6 μM.

Time-correlated single photon counting
Time-correlated single-photon counting (TCSPC) was carried out using a DeltaFlex. The data were subsequently fitted to a sum of exponentials; FðtÞ = ∑ i A i expðÀk i tÞ by deconvolution with the instrument response function (IRF). The IRF was obtained through light scattering from Ludox particles dispersed in solution. The FWHM was~200 ps, which afforded a temporal timeresolution of ≥100 ps.

Ultrafast transient absorption spectroscopy
Ultrafast transient absorption spectroscopy was performed using a custom-built transient absorption (TA) set-up 42 . All laser pulses used were derived from a Yb:KGW laser system (Carbide, Light Conversion), providing pulses with 1028 nm, 54 µJ, 250 fs at 60 kHz repetition rate. Approximately 4 µJ pulse −1 was used to generate white light (WL) generation in a 5 mm-thick sapphire window, which served as the probe (range~550-850 nm). The remaining~50 µJ pulse −1 was used to generate 514 nm light by second-harmonic generation in a BBO crystal, which served as the pump. The polarization of the probe was at the magic angle (54.7°) relative to the pump. The pump pulse train was chopped at 30 kHz, attenuated to deliver~0.8 µJ pulse −1 at the sample, and delayed relative to the pump using a motorised translation stage. Both pump and probe pulses were independently focussed onto the sample using curved mirrors. The transmitted WL was recollimated using a lens. A polariser was used to minimise the scattering of the pump by the sample. The WL was passed through a slit to select the central portion of the beam and dispersed via a prism onto a line-scan camera (LightWise Allegro, Imaging Solutions Group). The sample was contained in a standard cuvette of 1 mm path length, which was translated to reduce sample degradation. TA experiments on a given sample typically took 10 min to complete, which avoided overall sample degradation. The concentration of samples was 5 mg ml −1 .

Statistical analysis
All error bars represent a 95% confidence interval. All statistics and graphical analyses were performed using GraphPad Prism 8 (GraphPad Software, inc.). All data points represent independent experiments.

Reporting summary
Further information on research design is available in the Nature Research Reporting Summary linked to this article.