ASU team discovers a new take on early evolution of photosynthesis

A team of scientists from Arizona State University’s School of Molecular Sciences has begun rethinking the evolutionary history of photochemical reaction centers (RCs). Their analysis was recently published online in Photosynthesis Research and describes a new pathway that ancient organisms may have taken to evolve the great variety of photosynthetic RCs seen today across bacteria, algae, and plants. The study will go into print later this summer in a special issue dedicated to photochemical RCs.

Photosynthesis is the process by which plants, algae and some bacteria use the energy from the sun to power their metabolism. Plants and algae use this light energy to make sugars from water and carbon dioxide, releasing the oxygen that we breathe. But certain bacteria carry out a simpler form of photosynthesis that does not produce oxygen, and is believed to have evolved first.

The molecular engines in all photosynthetic organisms that convert light energy to chemical energy are called photochemical reaction centers. RCs are chlorophyll-containing proteins found in the cell membrane. Their first appearance and subsequent diversification has allowed photosynthesis to power the biosphere for over 3 billion years, in the process supporting the evolution of more complex life forms.

Two types of RCs exist today: Type I RCs support metabolism by moving electrons to soluble proteins, while Type II RCs move electrons to membrane-associated molecules. However, evidence has been building in the lab of professor Kevin Redding that the RC from the heliobacteria may be able to perform both of these functions, making it a functional hybrid of the two RC types.

The heliobacterial RC is thought to be one of the simplest RCs still around today. It is homodimeric, meaning that its core is composed of two copies of the same protein. This contrasts with the two RCs from oxygen-producing organisms like plants whose core is heterodimeric, having their core composed of two similar, but not identical, proteins.

It is believed that the RC arose only once during Earth’s history, and that all the RCs around today are distantly related to that original ancestor. Over time, these RCs have changed to perform different chemistries. While the amino acid sequences have changed a great deal, astonishingly, the overall structure of RCs has remained similar. The team believes that the ancestral reaction center (ARC) was simpler than the versions that exist today. This ARC was probably homodimeric and interacted with molecules in the membrane, like the modern Type II RCs (and the heliobacterial RC), instead of with soluble proteins.

It is very difficult to reconstruct these evolutionary steps, which took over 3 billion years to occur. One way in which this is generally done is to compare the amino acid sequences of the proteins and note the number of differences between them, assuming that more similarity means that they are more closely related. In their study, however, the team cautions against relying heavily on this method for RCs. The sequence differences are just too numerous and too much time has passed to obtain reliable information from this method.

They instead compared the positions of protein structural elements and chlorophylls within the RCs. In essence, they focused more on the structure and function of the RCs to reconstruct the evolutionary history, starting by making predictions about the ARC’s structure and function.

The team envisions that the ARC, in its simplest form, was probably rather inefficient at its chemistry. Its job was to use the energy of sunlight to provide two electrons to a membrane-associated molecule called a quinone. However, the ARC likely could loosely bind two quinone molecules, one on each side of the core. With two identical-looking quinones, the ARC was not able to prioritize which quinone would get electrons, making it less likely that either would get the two it needed.

This problem was solved in two different ways. In the lineage that led to the modern Type II RCs, the core changed from homodimeric to heterodimeric, which allowed the RC to prioritize which quinone it gave electrons to, accelerating the chemistry. In the lineage that led to the modern Type I RCs, the core remained homodimeric, but a metal cluster was added so that the first electron would end up there, facilitating its delivery to the quinone that received the next electron.

Once the ARC had acquired the metal cluster, thus becoming the ancestor to all modern Type I RCs, more changes occurred to further direct electrons to a soluble acceptor, which resulted in extracting more energy for the cell’s metabolism. These included changes in the positions and identities of the chlorophyll cofactors. Much of the later changes in the Type I RCs were driven by the need to deal with the presence of oxygen, as the unstable intermediates within RCs can react with oxygen to generate very damaging molecules. In the opinion of the ASU team, the heliobacterial RC retains clear vestiges of the changes leading to the early Type I RC and that understanding the fine details in how modern RCs work allows for informed hypotheses about how they evolved.

The team included Greg Orf, Christopher Gisriel and Kevin E. Redding. This work was funded by the Division of Chemical Sciences, Geosciences, and Biosciences, Office of Basic Energy Sciences, of the U.S. Department of Energy through Grant (DE-SC0010575).