Reaction centers (RCs), integral membrane proteins that mediate the conversion of light into chemical energy, were crystallized by two different vapor diffusion techniques. In one method, small amphipathic molecules (1,2,3-heptanetriol and triethylammonium phosphate) were added to the RCs that had been solubilized in detergent. In the second method, crystallization occurred near the phase boundaries of a two-phase system created by the addition of polyethylene glycol and NaCl to RCs in ocyl /3-D-glucoside. Several different crystal forms were obtained; two were analyzed by x-ray diffraction. One was monoclinic (space group P2) with fi = 105°, and a = 70 A, b = 105 A, and c = 85 A, two RCs per unit cell, and one RC per asymmetric unit; the crystal diffracted to 3.5 A at 17TC. The other crystal form was orthorhombic (space group C222) with a = 185 A, b = 170 A, and c = 105 A, with eight RCs per unit cell and one RC per asymmetric unit. Reversible light-induced EPR signals of the primary donor (bacteriochlorophyll dimer) showed that the RCs in the crystal were fully active. From the angular dependence of the EPR signal the molecular g anisotropy of the bacteriochlorophyll dimer was deduced to be go1-= (64 -+-3) X 10-5. Linear dichroism measurements were performed on the monoclinic crystal. The two bands at 535 and 544 nm assigned to the Q1 transitions of the bacteriopheophytins were resolved and preliminary orientations of some of the pigments were obtained.The reaction center (RC) is an integral membrane protein that mediates the conversion of electromagnetic energy (light) into chemical energy. The RC from the purple bacterium Rhodopseudomonas sphaeroides is composed of three polypeptide chains designated L, M, and H present in a 1:1:1 stoichiometry with a total molecular weight of -100,000. The following cofactors (reactants) involved in the energy transfer process are attached to the RC: four bacteriochlorophylls (BChl), two bacteriopheophytins (BPhe), two ubiquinones, and one nonheme iron (for review see ref. 1).Although a great deal of work has been done on the characterization of RCs, there is little information available about their three-dimensional structure. The lack of knowledge of the exact spatial relationships between the reactants makes it difficult to understand quantitatively the details of the energy transfer process, in particular the remarkably high quantum efficiency of the photosynthetic process. Accordingly, we have begun structural studies on crystals of RCs from R. sphaeroides.Recently several membrane proteins have been crystallized (2-4), including RCs from the photosynthetic bacterium Rhodopseudomonas viridis (5), and some structural studies have been performed (6, 7). However, since RCs from R. sphaeroides are smaller and have been characterized in more detail than those from R. viridis, studies on R. sphaeroides may be easier to interpret. In this work we describe methods of obtaining crystals from R. sphaeroides and present preliminary result of x-ray diffraction, electron pa...