Prior to the evolution of complex biochemical machinery, the growth and division of simple primitive cells (protocells) must have been driven by environmental factors. We have previously demonstrated two pathways for fatty acid vesicle growth in which initially spherical vesicles grow into long filamentous vesicles; division is then mediated by fluid shear forces. Here we describe a different pathway for division that is independent of external mechanical forces. We show that the illumination of filamentous fatty acid vesicles containing either a fluorescent dye in the encapsulated aqueous phase, or hydroxypyrene in the membrane, rapidly induces pearling and subsequent division in the presence of thiols. The mechanism of this photochemically driven pathway most likely involves the generation of reactive oxygen species, which oxidize thiols to disulfide-containing compounds that associate with fatty acid membranes, inducing a change in surface tension and causing pearling and subsequent division. This vesicle division pathway provides an alternative route for the emergence of early self-replicating cell-like structures, particularly in thiol-rich surface environments where UV-absorbing polycyclic aromatic hydrocarbons (PAHs) could have facilitated protocell division. The subsequent evolution of cellular metabolic processes controlling the thiol:disulfide redox state would have enabled autonomous cellular control of the timing of cell division, a major step in the origin of cellular life.origin of life | vesicles O ne model for the nature of the earliest and simplest cells, or protocells, is that they consisted of a self-replicating membrane compartment (vesicle) that encapsulated a self-replicating genetic polymer (1). The emergence of any genetically encoded function that enhanced protocell reproduction or survival would have marked the beginnings of Darwinian evolution and, thus, of biology itself. We have been attempting to test various aspects of this model for the origin of cellular life through the laboratory construction and characterization of model protocells (2, 3). A necessary and complementary aspect of this program is the exploration of environmental scenarios in which external inputs of matter and energy could drive the replication of the genetic material of a protocell (4), as well as protocell membrane growth and division (5, 6). For example, we recently showed that activated nucleotides, added to a suspension of model protocells, could cross the vesicle membrane and copy encapsulated nucleic acid templates (4). We have also shown that large multilamellar fatty acid vesicles can grow by absorbing fatty acid molecules from added fatty acid micelles (6). This growth pathway begins with the emergence of a thin membranous filament from the side of the initially spherical vesicle; the filament grows and gradually incorporates the contents and membranes of the parent vesicle, which is transformed into a long filamentous vesicle. Under modest shear forces, the filamentous vesicle divides into multiple da...