Properties and Crystal Structure of the Cereibacter sphaeroides Photosynthetic Reaction Center with Double Amino Acid Substitution I(L177)H + F(M197)H

The photosynthetic reaction center of the purple bacterium Cereibacter sphaeroides with two site-directed mutations Ile-L177–His and M197 Phe–His is of double interest. The substitution I(L177)H results in strong binding of a bacteriochlorophyll molecule with L-subunit. The second mutation F(M197)H introduces a new H-bond between the C2-acetyl carbonyl group of the bacteriochlorophyll PB and His-M197, which is known to enhance the stability of the complex. Due to this H-bond, π -electron system of P finds itself connected to an extensive H-bonding network on the periplasmic surface of the complex. The crystal structure of the double mutant reaction center obtained with 2.6 Å resolution allows clarifying consequences of the Ile L177 – His substitution. The value of the P/P+ midpoint potential in the double mutant RC was found to be ~20 mV less than the sum of potentials measured in the two RCs with single mutations I(L177)H and F(M197)H. The protein environment of the BChls PA and BB were found to be similar to that in the RC with single substitution I(L177)H, whereas an altered pattern of the H-bonding networks was found in the vicinity of bacteriochlorophyll PB. The data obtained are consistent with our previous assumption on a correlation between the bulk of the H-bonding network connected with the π-electron system of the primary electron donor P and the value of its oxidation potential.


Introduction
Photosynthetic reaction centers are integral membrane complexes responsible for the extremely efficient conversion of light energy into the chemical energy of separated charges. The crystal structure of the reaction center (RC) of the purple nonsulfur bacterium Cereibacter (C.) sphaeroides shows that this complex consists of three subunits and ten cofactors ( Figure 1A) [1]. The L and M protein subunits and cofactors are related to each other by an approximate two-fold symmetry axis [2]. Cofactors are represented by four bacteriochlorophylls (BChl), two bacteriopheophytins (BPeo), two quinones, one carotenoid molecule, and a non-heme iron atom and are arranged in two membranespanning branches, A and B. Only one, A branch, is active in photosynthetic electron transfer. Two BChls, P A and P B , are combined into a dimer P that serves as a primary electron donor. An important property of P is the midpoint potential (E m ) P/P + which is related to the energy level of P* after light excitation. In the wild-type RCs of purple bacteria, cofactors interact with integral L-and M-subunits through relatively weak non-covalent contacts. Figure 1B shows four BChl molecules in the C. sphaeroides RC and some amino acid residues from their environment. Histidine residues, L173 and M202, coordinate central Mg 2+ atoms of BChls P A and P B , respectively, and His-M182 is the ligand of BChl B B . In native C. sphaeroides RC, the C2-acetyl carbonyl group of the BChl P A forms an H-bond with

Construction of the mutant strain
The I(L177)H and F(M197)H mutations previously introduced [11,12] were combined together in puf-operon by simple cloning using available unique restriction sites [11]. Polyhistidine tag (6His) was introduced from the 3′-end of the puf-M gene, similar to what was previously described [13]. The modified puf-operon with the mutations was cloned into the broad-host-range vector pRK415, containing DNA fragment that included the pufLMX genes. The resulting plasmid was transferred into C. sphaeroides strain DD13 [14] through conjugative crossing to give a recombinant strain with the RC-only phenotype. The control pseudo wild-type strain was similarly made using the DD13 strain, complemented by a wild-type copy of the pufLMX genes.

Bacterial growth and reaction center purification
The growth of recombinant bacterial strains under dark semi-aerobic conditions has been described elsewhere [11]. The cells were harvested and then broken by ultrasonication, and membranes were sedimented by ultracentrifugation. Reaction centers were solubilized using lauryldimethylamine oxide (LDAO) (Sigma-Aldrich, Missouri, USA) and then purified by passage through Ni-NTA agarose column (Serva, Heidelberg, Germany). After the purification of the RCs, the detergent was replaced as previously described [15]. The purified RCs were dissolved in 20 mM Tris-HCl buffer (pH 8.0) (Helicon, Moscow, Russia) containing 0.2% sodium cholate (Sigma-Aldrich, Missouri, USA) or 0.05 % Triton X-100 (Helicon, Moscow, Russia).
2.3. Thermal stability, adsorption spectroscopy, and redox potential measurements Previously, it was shown that substitution of Ile-L177 for His in the RC of C. sphaeroides near BChl B B and P A resulted in unexpectedly strong binding between one of these chromophores and L-subunit, which was stable during SDS-PAGE under a variety of denaturing conditions [5]. The appearance of a new band at 638 nm in the absorption spectrum of the I(L177)H mutant RC indicated that the central Mg 2+ atom of one out of four BChls became hexa-coordinated, while the other BChls remained penta-coordinated [6]. Treatment of the isolated RC with sodium borohydride revealed that the pigment strongly bound to the protein is BChl P A [7]. Later, the crystal structure of RC I(L177)H was obtained with a relatively low resolution of 2.9 Å [6]. The difference electron density map showed low sigma peaks adjacent to the central Mg 2+ atom of BChl B B , indicating the potential presence of a water molecule. Computer modeling proposed the involvement of two water molecules in the β-coordination of the BChl B B , however, a higher resolution structure is needed for a conclusion on this issue. The question concerning the nature of the strong attachment of BChl P A to the RC protein also remains open.
We suggested that decreased thermal stability of the I(L177)H mutant RC structure, shown in previous work [7], could be one of the possible reasons for the poor quality of the RC crystals and the resulting insufficient resolution of the crystal structure [6]. It is known that H-bond formation between the protein environment and the C2-acetyl carbonyl groups of the BChl dimer contributes to the strengthening of the local structure of the C. sphaeroides RC, increasing its resistance to elevated temperatures and pressure [8,9]. Based on the recently resolved crystal structure of the RC F(M197)H, it was found that the increased stability of this complex is associated with the incorporation of the C2-acetyl carbonyl group of BChl P B into the H-bonding network surrounding this cofactor. It was also suggested that the size and pattern of the H-bonding networks near P can affect the oxidation potential of the BChl dimer [10]. However, more experimental data are needed to support this assumption. While the H-bonding networks associated with proton transfer and secondary quinone reduction are well characterized, the H-bonding clusters on the periplasmic side of the purple bacteria RCs are less studied and their role requires further investigation.
We have combined I(L177)H and F(M197)H mutations in C. sphaeroides RC to increase the stability of its structure and thereby increase the probability of obtaining the crystal structure of this complex with higher resolution. This work introduces the new double mutant RC and describes its spectral properties and oxidation potential of the primary electron donor P. X-ray crystal structure of the RC I(L177)H + F(M197)H, obtained with a resolution of 2.6 Å, clarifies some details of unusually strong pigment-protein interaction resulting from the Ile→His substitution at L177 position and shows that a new water molecule appears from β-side of BChl B B , which is responsible for hexa-coordination of the central Mg 2+ atom of this cofactor. In addition, the crystal structure provides data in support of the previously stated assumption about the correlation between the bulk of the H-bonding network in the vicinity of the BChl dimer and the value of the oxidation potential of the primary electron donor.

Construction of the Mutant Strain
The I(L177)H and F(M197)H mutations previously introduced [11,12] were combined together in puf -operon by simple cloning using available unique restriction sites [11]. Polyhistidine tag (6His) was introduced from the 3 -end of the puf -M gene, similar to what was previously described [13]. The modified puf -operon with the mutations was cloned into the broad-host-range vector pRK415, containing DNA fragment that included the puf LMX genes. The resulting plasmid was transferred into C. sphaeroides strain DD13 [14] through conjugative crossing to give a recombinant strain with the RC-only phenotype. The control pseudo wild-type strain was similarly made using the DD13 strain, complemented by a wild-type copy of the puf LMX genes.

Bacterial Growth and Reaction Center Purification
The growth of recombinant bacterial strains under dark semi-aerobic conditions has been described elsewhere [11]. The cells were harvested and then broken by ultrasonication, and membranes were sedimented by ultracentrifugation. Reaction centers were solubilized using lauryldimethylamine oxide (LDAO) (Sigma-Aldrich, Missouri, USA) and then purified by passage through Ni-NTA agarose column (Serva, Heidelberg, Germany). After the purification of the RCs, the detergent was replaced as previously described [15]. The purified RCs were dissolved in 20 mM Tris-HCl buffer (pH 8.0) (Helicon, Moscow, Russia) containing 0.2% sodium cholate (Sigma-Aldrich, Missouri, USA) or 0.05 % Triton X-100 (Helicon, Moscow, Russia).

Thermal Stability, Adsorption Spectroscopy, and Redox Potential Measurements
Thermal stability of the RCs was studied in Tris-Triton buffer with 250 mM NaCl by monitoring thermo-dependent changes of the Q Y band amplitude at 48 • C as previously described [15]. Absorption spectra were recorded using a Shimadzu UV-1800 spectrophotometer (Shimadzu, Kyoto, Japan) at room temperature. Sodium ascorbate (1 mM) was added to samples to maintain the primary electron donor in a reduced state. The P/P + midpoint potential was determined by chemical titrations using potassium ferricyanide and sodium ascorbate as previously described [6].

Reaction Center Crystallization and Data Analysis
Trigonal crystals of the reaction center with the double mutation I(L177)H + F(M197)H, space group P3 1 21, were grown using the hanging drop vapor diffusion method as previously described in detail [6]. X-ray diffraction data were collected at the P11 beamline PETRA III electron storage ring (Hamburg, Germany) using cryo-cooled crystals. The crystal used for data collection diffracted to a higher resolution limit of 2.6 Å. The diffraction data were processed and scaled using XDS [16]. Molecular replacement was performed with Phaser [17], using the coordinates of the I(L177)H mutant RC structure from C. sphaeroides (PDB ID: 3V3Z) [6] as the search model. Data collection and refinement statistics are given in Table 1. Rigid body refinement was carried out before refinement using restrained maximum likelihood refinement in REFMAC 5.0 [18]. Manual rebuilding of the model was carried out in Coot [19]. The final cycle with an occupancy refinement was performed in Phenix [20]. The coordinates and structure factors of double mutant RC have been deposited in the Protein Data Bank (PDB ID: 8C3F). Figures were prepared using the program PyMol [21].

Absorption Spectra
The mutant RC with the double substitution I(L177)H + F(M197)H was stably assembled in photosynthetic membranes and the yield of the RC after purification was similar to that of the wild-type RC from the same amount of the cell mass. The absorption spectrum of the wild-type RC measured at room temperature shows the Q Y P band at 865 nm, the Q Y B band at 804 nm, and the Q Y H band at 759 nm [22]. In the short wavelength region, the BChls and BPheos of the wild-type RC give rise to asymmetric absorbance bands with main peaks at 599 and 533 nm, respectively. Previously, it was shown that the absorption spectrum of RC F(M197)H was similar to the spectrum of the wild-type RC [23]. As described by [11], the room temperature absorption spectrum of RC I(L177)H showed a noticeable 18 nm blue shift and a diminished amplitude of the Q Y P band near 847 nm, a diminished amplitude of the Q Y B band, as well as decreased absorption in the Q X region of BChl absorption near 600 nm. The absorption spectrum of RC I(L177)H + F(M197)H showed similarity to that of RC I(L177)H, except that the blue shift of the Q Y P band was less pronounced and the maximum of this band was observed at 854 nm ( Figure 2).

Absorption spectra
The mutant RC with the double substitution I(L177)H + F(M197)H was stably assembled in photosynthetic membranes and the yield of the RC after purification was similar to that of the wild-type RC from the same amount of the cell mass. The absorption spectrum of the wild-type RC measured at room temperature shows the QY P band at 865 nm, the QY B band at 804 nm, and the QY H band at 759 nm [22]. In the short wavelength region, the BChls and BPheos of the wild-type RC give rise to asymmetric absorbance bands with main peaks at 599 and 533 nm, respectively. Previously, it was shown that the absorption spectrum of RC F(M197)H was similar to the spectrum of the wild-type RC [23]. As described by [11], the room temperature absorption spectrum of RC I(L177)H showed a noticeable 18 nm blue shift and a diminished amplitude of the QY P band near 847 nm, a diminished amplitude of the QY B band, as well as decreased absorption in the QX region of BChl absorption near 600 nm. The absorption spectrum of RC I(L177)H + F(M197)H showed similarity to that of RC I(L177)H, except that the blue shift of the QY P band was less pronounced and the maximum of this band was observed at 854 nm (Figure 2).  Thermal stability of the wild-type RC as well as mutant RCs I(L177)H, F(M197)H, and I(L177)H+F(M197)H was determined by recording thermo-dependent changes of the QY B band amplitude at 48°C in Tris-Triton buffer. It was shown that after 60 min of incubation in the spectrum of the wild-type RC, the amplitude of the QY B band at 804 nm decreased by 50%, whereas the spectra of the RCs I(L177)H, F(M197)H, and I(L177)H+F(M197)H demonstrated 55%, 40%, and 45% decreases, respectively ( Figure 3). These data show that, as expected, the addition of the F(M197)H mutation increases the thermal stability of RC I(L177)H, however, it remains lower than that of the single mutant RC F(M197)H.

P/P + midpoint potential
The value of the P/P + midpoint potential (Em P/P + ) of the double mutant RC was determined by redox titrations as 555 ±10 mV ( Figure S1, Supplementary). Previously, it was shown that the single mutation F(M197)H raises the value of Em P/P + by 125 mV [24] due to the formation of an H-bond between the C2-acetyl carbonyl group of BChl PB and the imidazole group of His-M197, whereas the substitution I(L177)H results in a decrease of the Em P/P + value by 50 mV [6]. Assuming that in the double mutant RC each of the mutations causes the same structural changes as in each RC with single substitutions, one would expect the resulting Em P/P + value to be ~575 mV. The crystal structure of RC I(L177)H + F(M197)H resolved in this study allows us to suggest a possible reason for the discrepancy between expected and experimentally observed mid-point potential P/P + (discussed below).

Crystal structure
The crystal structure of the double mutant reaction center was obtained with a resolution of 2.6 Å and an estimated maximal coordinate error of 0.31 Å (Table 1)

P/P + Midpoint Potential
The value of the P/P + midpoint potential (E m P/P + ) of the double mutant RC was determined by redox titrations as 555 ± 10 mV ( Figure S1, Supplementary). Previously, it was shown that the single mutation F(M197)H raises the value of E m P/P + by 125 mV [24] due to the formation of an H-bond between the C2-acetyl carbonyl group of BChl P B and the imidazole group of His-M197, whereas the substitution I(L177)H results in a decrease of the E m P/P + value by 50 mV [6]. Assuming that in the double mutant RC each of the mutations causes the same structural changes as in each RC with single substitutions, one would expect the resulting E m P/P + value to be~575 mV. The crystal structure of RC I(L177)H + F(M197)H resolved in this study allows us to suggest a possible reason for the discrepancy between expected and experimentally observed mid-point potential P/P + (discussed below).

Crystal Structure
The crystal structure of the double mutant reaction center was obtained with a resolution of 2.6 Å and an estimated maximal coordinate error of 0.31 Å (Table 1). After refinement, the structural model of RC I(L177)H + F(M197)H was compared with the structures of the wild-type RC (PDB ID: 3V3Y), RC F(M197)H (PDB ID: 7OD5), and I(L177)H (PDB ID: 3V3Z). In the structure of RC I(L177)H + F(M197)H, the protein environment of BChls B B and P A is similar to that in the previously described structure of RC I(L177)H [3]. A new electron density appears from the β-side of B B , which suggests the incorporation of a new water molecule ( Figure 4A). The structure shows that the water is located at a distance of 2.7 Å from the central Mg 2+ atom of B B , which is typical for the BChl axial ligands. This water is also 3.1 Å close to the imidazole group of His-L177, which is within the typical range for H-bond formation (Figure 4). BChls BB and PA is similar to that in the previously described structure of RC I(L177)H [3]. A new electron density appears from the β-side of BB, which suggests the incorporation of a new water molecule ( Figure 4A). The structure shows that the water is located at a distance of 2.7 Å from the central Mg 2+ atom of Вв, which is typical for the BChl axial ligands. This water is also 3.1 Å close to the imidazole group of His-L177, which is within the typical range for H-bond formation (Figure 4). The imidazole group of His-L177 points towards the methyl carbon of the pyrrole ring I of PA with the center-to-center distance between N and C atoms of 2.06 Å. According to the electron density map, imidazole forms a covalent bond with the methyl carbon of PA with a high degree of probability. Based on the structural data, we modeled pigmentprotein interactions that occur as a result of Ile→His substitution at the L177 site ( Figure  4B).
Comparison of the structures of the double mutant RC and RC F(M197)H in the proximity of BChl PB shows structural conservation in the main body of the protein as well as in the cofactor system. In both complexes, the imidazole group of His-M197 is located within the H-bond distance from the C2-acetyl carbonyl group of BChl PB. It was noted that the C2-acetyl group shows 29.7° out of plane rotation ( Figure 5), which is more significant compared with that observed in RC F(M197)H (20.7°) [10]. The data are consistent with spectral properties of RC I(L177)H + F(M197)H (as discussed below). The imidazole group of His-L177 points towards the methyl carbon of the pyrrole ring I of P A with the center-to-center distance between N and C atoms of 2.06 Å. According to the electron density map, imidazole forms a covalent bond with the methyl carbon of P A with a high degree of probability. Based on the structural data, we modeled pigment-protein interactions that occur as a result of Ile→His substitution at the L177 site ( Figure 4B).
Comparison of the structures of the double mutant RC and RC F(M197)H in the proximity of BChl P B shows structural conservation in the main body of the protein as well as in the cofactor system. In both complexes, the imidazole group of His-M197 is located within the H-bond distance from the C2-acetyl carbonyl group of BChl P B . It was noted that the C2-acetyl group shows 29.7 • out of plane rotation ( Figure 5), which is more significant compared with that observed in RC F(M197)H (20.7 • ) [10]. The data are consistent with spectral properties of RC I(L177)H + F(M197)H (as discussed below). Analysis of the RC I(L177)H + F(M197)H structure in the vicinity of PB ( Figure 6) shows that the main pattern of the previously described H-bonding network, which includes the C2-acetyl carbonyl group of BChl PB, the imidazole group of His-M197, side groups of Asn-M195, Ser-L158, Asp-L155, and Tyr-M198 and two water molecules (assigned as waters-C and -E in Figure 6 and [10]), is similar to that observed in the RC with the single substitution F(M197)H. The sigma level of the electron density map peak for the water-C is low (1.7) and not sufficient to assert its presence with confidence. However, this water is observed in the structures of the wild-type RC and RC F(M197)H [10] as part of Asn-M195, Ser-L158, Asp-L155, and Tyr-M198 and two water molecules (assigned as waters-C and -E in Figure 6 and [10]), is similar to that observed in the RC with the single substitution F(M197)H. The sigma level of the electron density map peak for the water-C is low (1.7) and not sufficient to assert its presence with confidence. However, this water is observed in the structures of the wild-type RC and RC F(M197)H [10] as part of their H-bonding networks. As shown in Figure 6, there is a high degree of probability that water-C is also present in the structure of the double mutant RC. The distances between the related side groups in the network are all within the range of 2.5-3.03 Å consistent with H-bond formation ( Figure 6). The only exception is the distance between water-C and the side group of Asp-L155, which exceeds 3.7 Å. Taking into account the coordinate error, it suggests that no H-bond forms between these groups in RC I(L177)H + F(M197)H. The absence of this H-bond is consistent with some shortening of the distance between water-C and the imidazole group of His-M197 (2.7 Å), compared with the structure of RC F(M197)H (3.1 Å) ( Figure 6). In addition, Figure 6B shows a change in the mutual arrangement of the Tyr-M198 and Asp-L155 side groups, indicating that Asp-L155 is shifted away from water-C in the double mutant RC structure.

Discussion
We have characterized spectral properties and mid-point potential P/P + of the double mutant RC I(L177)H + F(M197)H as well as presented the crystal structure of the complex with 2.6 Å resolution. It is shown that the spectral properties of the double mutant RC are similar to those of RC I(L177)H, except that the blue shift of the QY P band is less pronounced, namely 11 nm compared with 18 nm for RC I(L177)H. It was noticed that while a single mutation F(M197)H did not lead to evident changes in the spectral properties of It has been shown that in the wild-type RC of C. sphaeroides, an H-bonding network also presents on the periplasmic side of BChl P A [10]. The network includes the C2-acetyl carbonyl group of BChl P A , the imidazole group of His-L168, side groups of Asn-L166, Asp-M184, and Tyr-L169 and a water molecule assigned as water-D. In the crystal structure of RC I(L177)H + F(M197)H, the positions of the side groups of the aforementioned residues did not change significantly, compared with those in the wild-type and F(M197)H RC structures ( Figure S2 in Supplementary section). Although the sigma level of the electron density map peak for the water-D is low (1.5), its presence is indicated by the distance of this water from the side groups of Asn-L166 and Asp-M184, which is within the range of H-bond distances, similar to those in the wild-type and F(M197)H RCs. Thus, the data obtained show that the protein environment of BChls P A and B B is similar to that in the RC with single substitution I(L177)H.

Discussion
We have characterized spectral properties and mid-point potential P/P + of the double mutant RC I(L177)H + F(M197)H as well as presented the crystal structure of the complex with 2.6 Å resolution. It is shown that the spectral properties of the double mutant RC are similar to those of RC I(L177)H, except that the blue shift of the Q Y P band is less pronounced, namely 11 nm compared with 18 nm for RC I(L177)H. It was noticed that while a single mutation F(M197)H did not lead to evident changes in the spectral properties of RC, the addition of this mutation to RC I(L177)H led to a significant red shift of the Q Y P band. This spectral shift of the Q Y P band is likely a result of a much more substantial out-of-plane rotation of the C2-acetyl carbonyl group of BChl P B (29.7º) compared with that observed in the structure of RC F(M197)H (20.7º) under the same conditions. As discussed previously in detail [10], the energy of the P Q Y transition in the mutant RC F(M197)H appears to be affected both by the rotation of the acetyl group of P B , which causes a red shift of the P Q Y band, and by a small increase in the distance between the two BChls of the dimer that leads to a blue shift of the band. In RC F(M197)H, these opposing effects compensate for each other, and as a result, the absorption spectrum remained practically the same as in the wild-type RC [23]. The resolution of the double mutant RC crystal structure does not allow us to estimate possible changes in the distance between the BChl planes in the dimer P but we see much more pronounced out-of-plane rotation of the acetyl group of BChl P B and suggest that it causes an additional 7 nm red-shift of the P Q Y band compared to the absorption spectrum of RC I(L177)H.
The original goal of this work was to combine RC I(L177)H and F(M197)H mutations to increase the stability of the mutant RC to improve the resolution of its crystal structure. The data obtained demonstrate that RC I(L177)H + F(M197)H is slightly more thermostable than the wild-type RC but not as stable as RC F(M197)H. Nevertheless, after the introduction of an additional H-bond of P with its protein environment, we succeeded in improving the resolution of the crystal structure up to 2.6 Å. For the first time, an analysis of the structural consequences of the I(L177)H mutation in the C. sphaeroides RC was performed based on its crystal structure obtained with 2.9 Å resolution (PDB ID: 3V3Z) [6]. The model of pigment-protein interactions that arose as a result of the mutation was somewhat refined in this work. It is shown that only one new water molecule, rather than two, appeared on the β-side of B B and is suggested to be the 6 th -ligand of the Mg 2+ atom of this BChl. This water appears to donate H-bond to the imidazole group of His-L177, which is also in contact with the methyl group of the pyrrole ring-1 of BChl P A (Figure 4). The distance between the N and C atoms of these groups in the structure is 2.06 Å, which exceeds known distance characteristic for C-N covalent bond (~1.5 Å) [25]. The resolution of the double mutant RC crystal structure is not yet sufficient to unequivocally confirm the covalent nature of BChl -protein binding and to reveal the origin of this bond and needs further improvement. However, it should be noted that the potential reactivity of this (B)Chl methyl group is supported by the fact that in the Chl f structure in the pyrrole ring-I, instead of a methyl group, a vinyl group is present [26].
The mutant RC I(L177)H + F(M197)H presented in this work turned out to be of interest as an object that has a modified H-bonding network near the BChl dimer P. Recently, the presence of H-bonding clusters on the periplasmic surface of the C. sphaeroides RC was reported [10]. Comparative analysis of such networks in the structures of natural and mutant RCs of different purple bacteria allowed us to assume that the polar protein environment can specifically affect the oxidative potential of the primary electron donor. In particular, it was suggested that when the π-electron system of P is connected with these networks, there is a correlation between the value of E m P/P + and the patterns, sizes, and, apparently, the total strength of H-bonds in the clusters. The crystal structure of RC I(L177)H + F(M197)H provides data in support of this assumption.
The main pattern of the H-bonding network in the protein environment of BChl P B in the double mutant RC structure (Figure 4) was found to be similar to that observed in the F(M197)H mutant RC [10], with one exception. The 3.7 Å remoteness of the water-C from the side group of Asp-L155 exceeds the H-bond distance ( Figure 6B). If the H-bond between Asp-L155 and water-C is not formed, one H-bond falls out of the H-bonding network. As a result, the bulk of the network connected with BChl P B through imidazole His-M197 became not as extended as in the F(M197)H RC. We assume that this can explain why the value of E m P/P + in double mutant RC is~20 mV lower than the sum of changes in the mid-point potentials caused by each of the two mutations. One should also not exclude the possibility that a more significant out-of-plane rotation of the acetyl group of P B reduces its conjugation into the π-electron system of the macrocycle, affecting both the total strength of H-bonds in the network and the value of E m P/P + . The loss of one H-bond in the network may also serve as an explanation for the fact that the thermal stability of RC I(L177)H + F(M197)H turned out to be less than that of RC F(M197)H [10]. A possible reason for the non-formation of the H-bond between Asp-L155 and water-C in RC I(L177)H + F(M197)H may be associated with the effect of the above-mentioned strong binding of BChl P A with His L177, which is expected to shift P towards BChl B B . This assumption is consistent with more significant out-of-plane rotation of the C2-acetyl carbonyl group of P B , compared with that of RC F(M197)H.
H-bond networks on the periplasmic surface of purple bacterial RCs have long been noticed. The periplasmic surface of the C. spheroids RC is an area of short-term binding of soluble cytochrome c2, which donates electrons for oxidized P [27,28]. Acidic residues Asp-L155 and Asp-M184 ( Figure 6 and Figure S2) were shown to be among a few others on the RC surface that interact with basic residues on cytochrome c 2 . In the recent work of Allen et al., it was proposed that the wide-spread network on the periplasmic side of RC participate in a hydrogen-bonded linear pathway that transfers protons between the environment of P + and the membrane surface [29]. This pathway includes the amino acid residues Asp-L155, Ser-L158, Tyr-M198, Asn M195, and a few water molecules in the vicinity of P B (Figure 6 and [10]). The possible role of the symmetry related cluster of H-bonds near BChl P A remains to be clarified.
To summarize, the data obtained in this study clarify the details of the pigment-protein interactions that arose as a result of mutation I(L177)H. In addition, the crystal structure of RC I(L177)H + F(M197)H illustrates that protein surroundings can affect the oxidation potential of the primary electron donor by altering the parameters of the H-bonding networks connected with the π-electron system of P.