Biosynthesis of soluble carotenoid holoproteins in Escherichia coli

Carotenoids are widely distributed natural pigments that are excellent antioxidants acting in photoprotection. They are typically solubilized in membranes or attached to proteins. In cyanobacteria, the photoactive soluble Orange Carotenoid Protein (OCP) is involved in photoprotective mechanisms as a highly active singlet oxygen and excitation energy quencher. Here we describe a method for producing large amounts of holo-OCP in E.coli. The six different genes involved in the synthesis of holo-OCP were introduced into E. coli using three different plasmids. The choice of promoters and the order of gene induction were important: the induction of genes involved in carotenoid synthesis must precede the induction of the ocp gene in order to obtain holo-OCPs. Active holo-OCPs with primary structures derived from several cyanobacterial strains and containing different carotenoids were isolated. This approach for rapid heterologous synthesis of large quantities of carotenoproteins is a fundamental advance in the production of antioxidants of great interest to the pharmaceutical and cosmetic industries.

T he human body is constantly exposed to external (ultraviolet radiation, pollution, cigarette smoke, toxic chemicals) and internal (side reactions of respiration, oxidation of nutrients) factors which induce the formation of Reactive Oxygen Species (ROS). Due to the harmful effects of ROS, the pharmaceutical and cosmetic industries have a significant interest in the production of new antioxidant molecules. For many applications, the medium in which the anti-oxidant effect is desired is water-based and requires a hydrophilic antioxidant. Water soluble carotenoid proteins fit these requirements. Carotenoids are widely distributed natural pigments which play important roles in photosynthesis, nutrition and illness prevention. They have a protective role in photosynthetic and non-photosynthetic organisms including humans by serving as protective colorants or by quenching singlet oxygen ( 1 O 2 ) and free radicals induced by exogenous sensitizers or produced by metabolic processes (reviews [1][2][3][4]. Carotenoids which are relatively hydrophobic molecules, typically occur solubilized in membranes or non-covalently attached to membrane or soluble proteins. In photosynthetic organisms, they are mainly found in the membrane-embedded, chlorophyll-containing-antennae where they have the dual activities of harvesting solar energy and quenching excess energy and 1 O 2 (see reviews 1,5 ). A number of water soluble carotenoid proteins from photosynthetic organisms have also been characterized [6][7][8] . The cyanobacterial Orange Carotenoid Protein (OCP) is one of the best characterized soluble carotenoid proteins. We have recently demonstrated that the OCP is an excellent antioxidant--better than vitamin C, trolox, tocopherol and isolated carotenoids 9 . The OCP protects cyanobacteria by quenching the 1 O 2 formed in reaction centers and antennae 9 . It was first described by Holt and Krogmann in 1981 10 and is present in the majority of cyanobacteria containing phycobilisomes (PBs), the large extra-membrane antenna formed by blue and red phycobiliproteins 11 .
The OCP is a photoactive protein 12 ; it is essential for a photoprotective mechanism that decreases the excitation energy arriving at photochemical reaction centers 13 . The OCP has an a-helical N-terminal domain (residues  and an a/b C-terminal domain (residues 190-317) (Fig. 1A) 14 . The carotenoid, 39-hydroxyechinenone (hECN), spans both domains which are joined by a flexible linker. The presence of a ketocarotenoid is essential for OCP photoactivity 15 . Light absorption by the carotenoid induces conformational changes in the carotenoid and in the protein that are essential for its photoprotective function 12 (Fig. 1B). In darkness, the OCP is orange (OCP o ); upon illumination, it becomes red. The red form (OCP r ) is the active form of the protein 12,15 . Only OCP r is able to bind the PBs. Once the OCP r is bound, the carotenoid interacts with a chromophore of the PB core and quenches the excitation energy [16][17][18] . This photoprotective mechanism is activated by blue-green light but not by orange or red light that are not absorbed by the carotenoid. However, the OCP photoprotects cyanobacteria from strong orange-red light; this protection is related to the 1 O 2 quenching activity of the OCP 9 .
Due to the outstanding antioxidant properties of carotenoids and their role in human health, substantial effort has been devoted to the engineering of noncarotenogenic bacteria to produce high quantities of these colorants; this also requires the development of methods to isolate the carotenoids from the engineered microorganisms (reviews [19][20][21][22] ). For many applications, a water soluble antioxidant is needed. The soluble OCP which is an excellent 1 O 2 quencher, is an ideal candidate. However, to-date there are no reports showing that it is possible to insert a carotenoid molecule in a protein in E.coli. Todate, genes encoding carotenoid proteins have been expressed in E.coli to isolate the apo-protein (protein without carotenoid) and then the carotenoid is attached to the apo-protein by in vitro reconstitution (examples 20,[23][24][25]. The OCP has been isolated from the WT cyanobacterial strains Synechocystis PCC 6803 (thereafter Synechocystis) and Arthrospira maxima or from Synechocystis mutants overexpressing WT or mutated OCPs 12,14,26-28 . This, however, is a labor-intensive process because of the low concentration of the OCP in cyanobacterial cells. Indeed, even when using OCP-overexpressing strains purification requires 3 weeks to obtain 40 mg protein from 30 L of cyanobacteria cells (A Wilson and D Kirilovsky, unpublished data).
Here we describe the construction of E.coli strains that are able to synthesize large amounts of OCP homologs from different cyanobacterial strains incorporating various carotenoids in vivo. This fast holo-OCP production has already enabled us to further understand the function of different carotenoids in OCPs, for example that canthaxanthin-OCPs are very good energy and 1 O 2 quenchers. The work described here is important not only to accelerate the elucidation of the OCP photoprotective mechanism by rapid synthesis of variant OCPs, but promises to enable the isolation and characterization of other carotenoid proteins with potential applications for promoting human health.

Results
Biosynthesis of His-tagged holo-OCPs in E.coli cells. The aim of our work was to synthesize holo-OCPs (OCPs attaching one carotenoid molecule) from Synechocystis, Arthrospira and Anabaena strains in E.coli cells. For this purpose, the genes coding for enzymes involved in the synthesis of the desired carotenoids (supplementary Fig. 1) and the ocp gene must be expressed in the same cell. It is known that in Synechocystis and Arthrospira OCP binds hECN 10,14 . Previous work showed that it is difficult to obtain large quantities of this carotenoid in E.coli cells 29,30 . We decided to express the ocp gene in the presence of two other ketocarotenoids: echinenone (ECN) and canthaxanthin (CAN). Synechocystis OCP is able to bind ECN and the ECN-OCP is photoactive and induces PB fluorescence quenching 27 . In contrast, Arthrospira OCP weakly binds ECN 31 . Prior to this study, nothing was known about the Anabaena OCP. Although we did not know if CAN-OCP would be active, we hypothesized that the carbonyl groups present in CAN rings could allow photoactivity and stabilization of the carotenoid binding.
The E. coli cells producing holo-OCPs carried three plasmids. The first plasmid, pAC-BETA (or pACCAR16DcrtX) 32,33 , contained the Erwinia herbicola (or Erwinia uredovora) operon carrying the four genes (crtB, crtE, crtI, crtY), which are necessary to synthesize bcarotene. In the second plasmid the crtO gene of Synechocystis or the crtW gene from Anabaena PCC 7210 was introduced. While CrtO is a monoketolase synthesizing mostly echinenone from bcarotene 34 , CrtW is a diketolase that catalyses the formation of canthaxanthin 35 (supplementary Fig. 1). The ocp genes were cloned in a third plasmid (pCDFDuet-1). In order to maintain the three plasmids within the same E.coli cell, the use of three different and compatible replication origins and three different antibiotic resistances was required (Fig. 2).
The operon containing the crtB, crtE, crtI and crtY genes was under the control of the constitutive crtE promoter. Thus, the bcarotene was constitutively synthesized in the E.coli cells. The crtO and crtW genes were under the control of the arabinose inducible promoter araBAD. The transcription of ocp genes was controlled by the IPTG-inducible T7lac promoter. A sequential induction of these genes was essential to isolate high quantities of holo-OCP. The expression of crtO or crtW genes was induced in E.coli containing a relatively high concentration of b-carotene. Subsequently the expression of ocp genes was induced in E.coli cells containing high concentrations of ECN or CAN in their membranes.
The E. coli cells carrying the crtO gene contained 15-25% of bcarotene, 70-80% ECN and 4-6% CAN. When the ocp genes were expressed in the presence of ECN, a mixture of apo-and holo-OCPs was obtained in all cases, but the proportion of holo-OCP varied ( Table 1). The presence of photoactive holo-OCPs was already detected in vivo. Orange cells containing holo-OCPs became red when they were illuminated with high intensities of white light (Fig. 3A). In contrast, yellow and orange E.coli cultures containing only genes involved in b-carotene and ECN (without the ocp gene) did not change colour upon illumination (Fig. 3A). Once the cells were broken, a notable difference in the colour of the supernatants (soluble fraction) was observed. The supernatant derived from E. coli cells synthesizing only carotenoids, because the ocp gene was not induced, was clear ( Fig. 3Bb) and the orange colour was concentrated in the membranes (Fig. 3Ba). The slight colour observed in the supernatant is attributable to a leak of the T7 promoter and the presence of a small concentration of OCP. In contrast, in the cells in which the ocp gene was induced, the supernatant was distinctly orange (Fig. 3Bc) indicating the presence of high concentrations of holo-OCPs. Moreover, under illumination the supernatant became red (Fig. 3Bd). Nevertheless, the membranes remained orange indicating that the presence of apo-proteins was not related to a lack of ECN in the cells.
The first Synechocystis ocp overexpressed genes contained an addition of 18 nucleotides coding for six His just before the stop codon (Syn-Ctag) or an extension of 45 nucleotides after the first ATG (Syn-pDuet) (supplementary Fig. 2 and Table 1). This extension which includes the sequence coding for six-His is already included in the commercial pCDFDuet-1 plasmid. Analysis of the resulting two isolated Synechocystis OCPs revealed that the addition of the Nterminal extension of 45 nucleotides increased the total amount of OCP present in the cells (from 4-6 mg/L to 18-22 mg/L) and the yield of holoOCP (from 25-40% (Syn-Ctag-ECN) to 35-45% (Syn-pDuet-ECN)) ( Table 1).
Since a modification on the N-terminus seemed to increase the yield of holoOCPs in E.coli cells, other ocp modifications were tested. In all cases (with the exception of one), nine to 45 nucleotides coding for a series of non-charged or charged amino acids were added just after the first ATG in the ocp gene containing a sequence coding for six-His in its 39 end (supplementary Fig. 2 and Table 1). In the construction lacking the C-terminal His-tag, 27 nucleotides including the sequence coding for six-His were added to the 59 end (Syn-3aaNtag) (supplementary Fig. 2 and Table 1). Analysis of the isolated Synechocystis OCPs showed that addition of 8 to 10 amino acids largely increased the yield of holo-OCP. More than 95% of isolated Synechocystis OCP contained a carotenoid molecule. When only 3 to 6 amino acids were   www.nature.com/scientificreports added, the yield of holoprotein also increased but slightly less (Table 1). Finally, addition of 9 amino acids, including 6 His, in the N-terminus, in the absence of C-terminal His-tag (Syn-3aaNtag) allowed the isolation of the largest quantity of holo-OCP containing almost no apo-protein: 30-35 mg holo-OCP ( Table 1). All of the isolated Synechocystis holo-OCPs contained more than 95% ECN with only traces of CAN (supplementary Fig. 3). These results suggested that a slight destabilisation of the OCP N-terminal arm is necessary to increase and/or to stabilize OCP carotenoid binding. In the OCP o , this arm interacts with the C-terminal domain and seems to stabilize the closed structure of the orange form 14,27 (Fig. 1). Arthrospira and Anabaena ocp genes, containing sequences coding for an His-tag in the N-or the C-terminus, were also expressed in E.coli cells synthesizing ECN. Although the His-tag in the Nterminus increased the yield of holo Anabaena and Arthrospira OCPs (to 60 and 40%, respectively), still a large amount of apo-OCP was present (Table 1). Since the membranes remained coloured indicating the presence of ECN, the low concentration of holo-OCPs was not related to insufficient carotenoid production. The holo-Anabaena and holo-Arthrospira OCPs contained mostly ECN with traces of CAN (supplementary Fig. 3).
In an attempt to increase the yield of Arthrospira and Anabaena holo-OCPs, the ocp genes were induced in E.coli cultures synthesizing CAN. This strain, carrying the crtW gene, contained 15-25% of b-carotene, 50-60% CAN, 7-9% ECN and 5-7% of an unknown carotenoid. Indeed, the presence of CAN increased the yield of holoprotein to 60% in the case of Arthrospira OCP. In contrast, the presence of CAN decreased the yield of holo-Synechocystis-OCP (Syn-3aaNtag-CAN) to 75-85% and of holo Anabaena-OCP (Ana-3aaNtag-CAN) to 40-45% (Table 1). While the holo-Anabaena-CAN-OCP contained mostly CAN with only traces of ECN, holo-Synechocystis-CAN-OCP contained 50-70% CAN and holo-Arthrospira-CAN-OCP contained only 50-55% CAN (supplementary Fig. 3). Our results indicated that the binding and/or the stability of carotenoids in the protein differs between Synechocystis and Arthrospira or Anabaena OCPs. Most probably only the presence of hECN will allow the isolation of more than 95% of holo Arthrospira or Anabaena OCPs.
Characteristics of the isolated OCPs. The isolated proteins are orange in darkness and red in strong light (Fig. 4A). Orange ECN-OCPs (OCP o ) absorbance spectra show maxima at 472 and 496 nm and a shoulder at 450 nm, comparable to the native cyanobacteria OCPs (Fig. 4A and supplementary Fig. 4A). The absorbance spectra of CAN-OCP o s were slightly red shifted compared to ECN-OCP o s with maxima at 475 and 500 nm ( Fig. 4A and supplementary Fig.  4B). The maximum of OCP r absorbance spectra was at 510 nm for ECN-OCPs and 525 nm for CAN-OCPs.
All three CAN-OCPs and Synechocystis and Arthrospira ECN-OCPs completely converted to their red form (OCP r ) under illumination (Fig. 4B). The kinetics of OCP o to OCP r photoconversion of the three CAN-OCPs and ECN-Arthropira-OCP were similar (t 1/2 5 4-7 sec) and faster than that of the ECN-Synechocystis OCP (t 1/2 5 18 sec) (Fig. 4B). The slower photoconversion of Synechocystis OCP compared to Arthrospira OCP was previously observed when the proteins were overexpressed in Synechocystis cells 31 . Anabaena ECN-OCP o only partially converted to OCP r , suggesting slight differences in the carotenoid-protein interaction in this protein (Fig. 4B). N-and Cterminal His-tagged Synechocystis OCPs presented similar conversion kinetics from OCP o to OCP r (Fig. 4C). When both termini of the protein were modified, an acceleration of OCP r accumulation was observed, suggesting a destabilization of the closed OCP o (Fig. 4C). Only one exception was observed: the addition of 8 charged amino acids hindered the conversion OCP o to OCP r (Fig. 4C).
The capacity of N-terminal His-tagged ECN-and CAN-OCPs to quench 1 O 2 was studied. Electron paramagnetic resonance (EPR) spin trapping was applied for 1 O 2 detection using TEMPD-HCl (2,2,6,6-tetramethyl-4-piperidone). When this nitrone reacts with 1 O 2 , it is converted into the stable nitroxide radical, which is paramagnetic and detectable by EPR spectroscopy. The production of 1 O 2 was induced by illumination of the photosensitizer methylene blue. Figure 5A shows the typical EPR signal of the nitroxide radical obtained after 3 min illumination (1000 mmol photons m 22 s 21 ) of a solution containing methylene blue and TEMPD-HCl in the absence or presence of the OCP. The presence of only 1.5 mM holo-OCP decreased the EPR signal between 65 and 85% and 4 mM OCP quenched nearly the entire EPR signal. These results indicated that all of the E. coli-derived OCPs are very good 1 O 2 quenchers (Fig. 5B). The slight differences in the efficiency of 1 O 2 quenching are likely due to the presence of higher concentrations of apo-protein for the same concentration of holo-OCP (see supplementary Fig. 5). Nevertheless, our results suggested that Arthrospira OCP has a slightly better activity as 1 O 2 quencher than Synechocystis OCP. In contrast, Anabaena-ECN-OCP had a slightly lower activity as 1 O 2 quencher. The nature of the bound carotenoid seemed not to influence the activity, as previously suggested 9 .
Finally, the ability of the OCPs to quench PB fluorescence was tested. Arthrospira and Synechocystis OCPs isolated from E coli were able to induce a large PB fluorescence quenching ( Fig. 6A and 6C). The activity of Synechocystis ECN-OCP was higher than that of Synechocystis CAN-OCP; the opposite was observed with Anabaena OCP since ECN-OCP was only partially converted to the red form (Fig. 6A). Addition of 6 to 10 amino acids to the N-terminus of the C-terminal His-tagged OCP partially inhibited the fluorescence quenching, suggesting that OCP binding to PBs is hindered ( Fig. 6B and supplementary Fig. 6B). The weaker binding of these modified OCPs was confirmed by the rapid fluorescence recovery observed when PBs-OCP complexes were incubated in darkness (Fig. 6C). In contrast, C-terminal His-tagged OCP remained mostly attached to the PBs (Fig. 6C). Both N-and C-terminal His-tagged Synechocystis ECN-OCPs isolated from E.coli were able to induce a large fluorescence quenching (Fig. 6A). However, a fast fluorescence recovery was observed only with Synechocystis N-terminal Histagged OCPs (Fig. 6C). Thus, the behaviour of OCPs is affected by the location of the His-tag.

Discussion
The use of soluble carotenoproteins as antioxidants to promote human health is an area of active research and, consequently, methods to produce them in high yields are important. The aim of our work was to synthesize holo-OCPs (OCPs attaching the carotenoid) in E.coli to develop a method for obtaining high quantities of carotenoproteins. Using the method described here, we obtained 200 times more holo-OCP in 20% of the time of previously established purifications involving overexpression in cyanobacterial cells (C Bourcier de Carbon, A Wilson and D Kirilovsky, unpublished data). In only four days more than 30 mg holo-Synechocystis OCP can be obtained from 1 L of E.coli cells using the construction Syn-3aaNtag-ECN.
The key elements of this production method are the choice of promoters and the sequential induction of genes. b-carotene must be present in the membrane before induction of ctrO or crtW genes leading to the synthesis of ECN or CAN, respectively. More importantly, ECN and CAN have to be synthesized in advance and present in the membrane before induction of the ocp gene. The presence of IPTG in the growth medium inhibits cell growth even at low concentrations. In addition, the T7lac promoter cannot be induced at temperatures higher than 30uC. In contrast, arabinose enhances cell growth and the araBAD promoter allows induction at 37uC. Thus, the carotenoid genes must be induced first with arabinose at 37uC to obtain a high concentration of carotenoid-containing cells and then, the carotenoprotein gene could be induced by IPTG addition at lower temperatures (20 to 28uC) to slow down protein synthesis, allowing protein folding and carotenoid binding.
The possibility of isolate holo-OCPs from E.coli cells constitutes a major advance for the investigation of the molecular mechanism of OCP since it facilitates rapid isolation of mutant proteins with new characteristics. The method has already permitted us to further characterize OCPs revealing different phenotypes related to specificity and strength of carotenoid binding. We demonstrate here that all OCPs are able to bind CAN and that CAN-OCPs are photoactive and able to induce large PB fluorescence quenching, like the native hECN-OCPs. This demonstration was not previously possible when OCPs were isolated by overexpression in Synechocystis cells since they contain only traces of CAN.
We also show here that Arthrospira, Anabaena and Synechocystis OCPs are characterized by different phenotypes in terms of specificity and strength of carotenoid binding. Synechocystis OCP binds and stabilizes ECN better than CAN. In contrast, Arthrospira and Anabaena OCPs preferentially bind CAN over ECN and have a low affinity for both carotenoids. It is difficult to explain these differences based in the comparison of Arthrospira and Synechocystis OCP o structures due to the high sequence identity among amino acids forming the carotenoid-binding pocket and the similar carotenoid orientation in the proteins (supplementary Fig 9A). Nothing is known about how the carotenoid is introduced in the apo-OCP. We can hypothesize that the OCP is synthesized by membrane bound ribosomes and that the carotenoid is introduced during the synthesis of the N-terminal domain. It could be possible that the amino acids involved in this initial binding differ from those in  Fig 9B and 9C).
The most unexpected result was the different behavior in PBs binding of Synechocystis OCPs with a His-Tag on the N-terminus compared to those with the tag on the C-terminus. In the past, all OCP characterizations and the construction of stable OCP-PBs complexes were made with isolated C-terminal His-tagged OCPs 12,16,28 . These OCPs, once bound to PBs at 0.5 or 0.8 M phosphate, remain almost permanently attached and the PBs remain quenched 16,28 . This characteristic allowed the isolation of quenched OCP-PB complexes 16,28 . Here, we show that the absence of the C-terminal His-tag largely accelerates the dark recovery of PB fluorescence, suggesting a decreased stability of bound OCP r . In contrast, OCP r binding kinetics were only slightly affected. In addition, a longer N-terminus in Cterminal His-tagged OCPs hinders the OCP binding and destabilizes the strong OCP r attachment to PBs. Our results strongly suggest that while the C-terminal His-tag increases the stability of OCP r -PB complexes, a longer N-terminus destabilizes this attachment.
Production of antioxidant molecules and proteins is a topic of considerable general interest to plant and human biologists since oxidative stress is involved in many processes leading to cell death or tissue damage. Here we show that all three recombinant OCPs show excellent activity as 1 O 2 quencher. Other soluble carotenoproteins also display good antioxidant properties like Asta P 6 and could be used in nutraceutics, cosmetics, etc. The possibility of engineering noncarotenogenic bacteria to produce carotenoproteins, like the OCP, which are present at relative low concentrations in the native organisms, constitutes a major breakthrough in efforts to obtain large quantities of carotenoid molecules as antioxidants.
In addition, the ability to synthesize holo-OCPs in E.coli is an important step in the construction of a biofuel (biomass) producing minimal microbe using sunlight as natural source of energy. In order to create these minimal entities new synthetic reaction centers containing the minimal number of components needed for electron transport are being constructed and antenna molecules are being attached to them to expand the spectral range for light absorption (for example [36][37][38][39][40] ). Presently, nothing is done to protect these systems. The OCP, a good quencher of excitation energy and singlet oxygen, is an excellent candidate for this function. It can regulate the excitation energy arriving to the reaction centers and quench the singlet oxygen formed by the inevitable secondary, dangerous reactions.

Methods
Amplification and cloning of Crt genes encoding enzymes involved in carotenoid synthesis and of ocp gene. The plasmids pAC-BETA (gift of Prof F. Cunningham) and pACCAR16DcrtX (gift of Prof G. Sandmann), which contain a P15A origin of replication and the crtB, crtE, crtI and crtY genes under the control of the promoter of crtE from Erwina herbicola and Erwina uredovora respectively, were used 32,33 . All results presented in this article were obtained with pAC-BETA.
The crtO and crtW genes were cloned into a modified Plasmid pBAD/gIII A (from Invitrogen) which contains a PBR322 origin of replication, an arabinose inducible promoter (araBAD) and an ampicillin resistance marker. The Plasmid pBAD/gIII A was first modified to avoid the export of the recombinant protein into the periplasmic space of the cells. For this purpose, the region encoding the ''gene III signal sequence'' was deleted. Primers used for the PCR mutagenesis were pBAD/gIIIAmut (F and R) (supplementary Fig. 7). The modified plasmid pBAD/gIII A was named pBAD. The Plasmid pBAD was digested with BgIII and EcoRI restriction enzymes to clone the crtO gene (slr0088) of Synechocystis PCC6803 or with NcoI and EcoRI restriction enzymes to clone the crtW gene (alr3189) of Anabaena PCC7120. Primers CrtO (F and R) and CrtW (F and R) were used to amplify crtO and crtW genes respectively (supplementary Fig. 7). The resulting plasmids were named pBAD-CrtO and pBAD-CrtW.
The ocp gene was cloned in the plasmid pCDFDuet-1 (from Novagen). The plasmid pCDFDuet-1 contains a CDF origin of replication, T7lac promoter and Streptomycin/ Spectinomycin resistance. The sequences of synthetic oligonucleotides (primers) used in the amplification and modification of all the genes are described in supplementary Fig. 7.
N-terminal His-tagged OCP. The pCDFduet-1 plasmid was digested with EcoRI and NotI to clone the different ocp genes (slr1963 from Synechosystis PCC6803, NIES39_N00720 from Arthrospira Platensis PCC7345 and all3149 from Anabaena PCC 7120). The primers OCPSyn-pDuet (F and R) were used to amplify the Synechocystis ocp gene (1104 nucleotides) using genomic DNA of Synechocystis PCC6803 as template. The primers OCPAna-pDuet (F and R) were used to amplify the Anabaena ocp gene (1076 nucleotides) using genomic DNA of Anabaena PCC 7120 as template. The primers OCPArthro-pDuet (F and R) were used to amplify the Arthrospira ocp gene (1355 nucleotides) using the plasmid pOF7345 as template 31 . The resulting PCR products were introduced into pCDFDuet-1 to create the pCDF-OCPSyn-pDuet, pCDF-OCPArthro-pDuet and pCDF-OCPAna-pDuet plasmids. In the OCP isolated from E.coli strains carrying these plasmids, an extension of 15 amino acids was present in the N-terminal of the OCP protein. This extension contains a His-tag comprising 6 His residues.
C-terminal His-tagged OCP. To obtain a C-terminal His-tagged Synechocystis OCP, it was first, necessary to abolish a NcoI site in the Synechocystis ocp gene sequence; accordingly the GCC sequence coding for Ala73 was changed to GCG (also coding for an alanine) using the plasmid pSK-OCPsyn-CterHisTagDFRP 12 . Then, pCDFDuet-1 was digested with NcoI and NotI to excise the N-terminal extension containing the His-tag initially present in this plasmid. The ocp genes containing a C-terminal His-Tag from Synechosystis PCC6803, Arthrospira Platensis PCC7345 and Anabaena PCC 7120 were cloned in the plasmid. The primers OCPsyn-Ctag (F and R) were used to amplify the ocp gene tagged in C-terminal domain from the plasmid pSK-OCPsyn-CterHisTagDFRP-A73A 12 . The primers OCParthro-Ctag (F and R) were used to amplify the ocp gene from the plasmid p2A7345His 31 . The primers OCPana-Ctag (F and R) were used to amplify the ocp gene from genomic DNA of Anabaena PCC 7120, the C-terminal His-tag was then added by PCR mutagenesis. The resulting PCR products were introduced into pCDFDuet-1 to create the pCDF-OCPsyn-Ctag, pCDF-OCParthro-Ctag and pCDF-OCPana-Ctag plasmids.
Modifications in His-tagged OCPs. The sequences added after the first ATG of the ocp Synechocystis gene are described in supplementary Fig. 2. The modifications (NC15, NC10, NC8, NC6, NC3, Mix15 and C8, Table 1) were introduced by directed mutagenesis, using the pCDF-OCPSyn-Ctag plasmid as template and the different oligonucleotides described in supplementary Fig. 7. The modification 3aaNtag (Table 1) was created by site-directed mutagenesis using the pCDF-OCPSyn-pDuet plasmid as template and the oligonucleotides described in supplementary Fig. 7. This mutagenesis causes the deletion of part of the OCP N-terminal extension present in the pCDF-OCPSyn-pDuet plasmid. The modification 3aaNtag was also created in the ocp genes of Arthrospira and Anabaena using the pCDF-OCParthro-pDuet and pCDF-OCPana-pDuet plasmids as templates and the oligonucleotides described in supplementary Fig. 7.
Transformation of E.coli cells and induction of genes. E.coli BL21-Gold (DE3) cells from Agilent Technologies (F-ompT hsdS(rB -mB-) dcm1 Tetr gal l(DE3) endA Hte) were used for OCP production. BL21 cells were transformed simultaneously with three plasmids: pAC-BETA, pBAD-CrtO (or pBAD-CrtW) and pCDF-OCP. The pCDF-OCP plasmid contains WT or modified sequences of ocp genes. The transformed E.coli cells were grown in the presence of three antibiotics (ampicillin (50 mg/ml), chloramphenicol (17 mg/ml) and streptomycin (25 mg/ml)) to maintain the three different plasmids in the same E.coli cell. For induction of the different genes, transformed E.coli were grown in TB medium at 37uC for 3-4 hours until OD 600 5 0.6. Then arabinose was added (0.02%) and the culture was grown overnight at 37uC. In the morning the cells are diluted with fresh medium and Arabinose 0.02% and they are grown at 37uC till OD 600 5 1-1.2. Then isopropyl b-Dthiogalactoside (IPTG) (0.2 mM) was added and the cells incubated overnight at 28uC. In the morning, the cultures were harvested and pellets were stored at 280uC until they were used.
OCP isolation and calculation of holo-OCP concentration. E.coli frozen cells were resuspended in the lysis buffer containing 40 mM Tris pH 8, 10% glycerol and 300 mM NaCl and were broken in dim light using a French Press. The membranes were pelleted and the supernatant was loaded onto a nickel column (Ni-Probond resin, Invitrogen). The OCP was eluted with 200 mM Imidazol. For isolation of Synechocystis, Arthrospira and Anabaena OCPs overexpressed in Synechocystis, an initial 50 mL Synechocystis culture was daily diluted during 2 weeks until reaching 30 L culture at OD800 5 0.8. The cells were precipitated and broken using a French Press. The OCP was isolated from the supernatant using two columns as described in 12 . Complete isolation took three weeks.
Total OCP concentration was measured using the Bradford method. At least five independent Bradford measurements of each isolated OCP were done. The concentration in mg/mL obtained by this method was converted to molar concentration using a MW of 35 kDa for the OCP. Holo-OCP concentration was calculated based in the fact that each holo-OCP binds one carotenoid molecule and thus, the molar concentrations of carotenoid and holo-OCP are identical. Carotenoid concentration was first calculated in mg/mL from the carotenoid absorbance at 496 nm and using A 1% 1 cm 5 2158 and then converted to molar concentration. The ratio between the molar concentration of holo-OCP and total OCP gives the percentage of holo-protein described in Table 1. When this ratio is around 1, we estimated that the preparation contained 100% holo-protein.
Absorbance spectra and photoactivity kinetics of OCP. Absorbance spectra and kinetics of photoactivity (illumination with 5000 mmol photons m 22 s 21 of white light) and dark recovery were measured in a Specord S600 (Analyticjena) at 18uC.
Measurements of OCP fluorescence quenching activity. Isolated Synechocystis PBs in 0.5 or 0.8 M phosphate were incubated in the presence of different modified OCP r s under illumination with strong blue-green light. The high concentration of phosphate was needed to maintain the integrity of PBs. Phosphate also influences the strength of OCP binding to PBs; it is stronger at 0.8 M than at 0.5 M phosphate 16 . The ratio of OCP to PB was 40 in all the experiments as previously described 16,18 . The concentration of the OCP for these experiments was calculated from the carotenoid absorbance spectra since only the OCP attaching a carotenoid is able to be photoactivated and to bind to PBs. The presence of apo-OCP did not hinder OCP r binding (supplementary Fig. 8).
Fluorescence quenching and recovery were monitored with a pulse amplitude modulated fluorometer (101/102/103-PAM; Walz, Effelrich, Germany). The fluorescence quenching was induced by 900 mmol photons m 22 s 21 of blue-green light (400-550 nm). All measurements were carried out at 23uC in 0.5 or 0.8 M phosphate buffer. The OCP was pre-converted to the red form by 10 min illumination with 5000 mmol photons m 22 s 21 of white light at 4uC. 1 O 2 detection by EPR spin trapping. Electron paramagnetic resonance (EPR) spin trapping was applied for 1 O 2 detection using TEMPD-HCl (2,2,6,6-tetramethyl-4piperidone) (100 mM). When this nitrone reacts with 1 O 2 , it is converted into the stable nitroxide radical, which is paramagnetic and detectable by EPR spectroscopy. The production of 1 O 2 was induced by illumination of the photosensitizer methylene blue (10 mM). The measurements were done in buffer 100 mM Tris-HCl pH 8 in the absence or in the presence of different concentrations of purified OCPs. The samples were illuminated for 3 min with white light (1000 mmol photons m 22 s 21 ). The EPR settings were as follows: hall center field 5 3467.270 G, microwave frequency 5 9.74 Ghz, power 5 4.450 mV and number of scans 5 12.
Measurement of carotenoid content in OCPs. The carotenoid content of E.coli cells and the isolated OCPs was analysed by High-Performance Liquid Chromatography (HPLC) and Mass spectrometry as described in 9 .