UCSB scientists synthesize first genetically evolved semiconductor material
June 14, 2012
UC Santa Barbara (UCSB) scientists have, for the first time, used genetic engineering and molecular evolution to direct the enzymatic synthesis of a semiconductor.
(This adds further details to our earlier news item on this.)
By controlling this directed evolution, it will be possible to evolve materials with specific capacities, like high performance in an evolved solar cell, for example, the researchers say.
“In the realm of human technologies it would be a new method, but it’s an ancient approach in nature,” said UCSB scientist Lukmaan Bawazer.
Using silicateins — proteins responsible for the formation of silica skeletons in marine sponges — the researchers were able to generate new mineral architectures by directing the evolution of these enzymes.
Silicateins, which are genetically encoded, serve as templates for the silica skeletons and control their mineralization, thus participating in similar types of processes by which animal and human bones are formed. Silica, also known as silicon dioxide, is the primary material in most commercially manufactured semiconductors.
In this study, polystyrene microbeads coated with specific silicateins were put through a mineralization reaction by incubating the beads in a water-in-oil emulsion that contained chemical precursors for mineralization: metals of either silicon or titanium dissolved in the oil or water phase of the emulsion.
As the silicateins reacted with the dissolved metals, they precipitated them, integrating the metals into the resulting structure and forming nanoparticles of silicon dioxide or titanium dioxide.
With the creation of a silicatein gene pool — the combination and recombination of various silicatein genetic materials — the scientists were able to create a multitude of silicateins, and then select for the ones with desired properties.
“This genetic population was exposed to two environmental pressures that shaped the selected minerals: The silicateins needed to make (that is, mineralize) materials directly on the surface of the beads, and then the mineral structures needed to be amenable to physical disruption to expose the encoding genes,” said Bawazer. The beads that exhibited mineralization were sorted from the ones that didn’t, and then fractured to release the genetic information they contained, which could either be studied, or evolved further.
The process yielded forms of silicatein not available in nature that behaved differently in the formation of mineral structures. For example, some silicateins self-assembled into sheets and made dispersed mineral nanoparticles, as opposed to more typical agglomerated particles formed by natural silicateins. In some cases, crystalline materials were also formed, demonstrating a crystal-forming ability that was acquired through directed evolution, said Bawazer.
Because silicateins are enzymes, with relatively long amino acid chains that can fold into precise shapes, there is the potential for more functionality than would be possible using shorter biopolymers or more traditional synthetic approaches. In addition, the process could potentially work with a variety of metals, to evolve different types of materials. By changing the laboratory-controlled environments in which directed evolution occurs, it will be possible to evolve materials with specific capacities, like high performance in an evolved solar cell, for example.
Research for this paper was supported by the U.S. Department of Energy.
Ref.: Lukmaan A. Bawazer et al., Evolutionary selection of enzymatically synthesized semiconductors from biomimetic mineralization vesicles, PNAS, 2012, DOI: 10.1073/pnas.1116958109 (open access)