ABSTRACT
Redesigning lignin, the aromatic polymer fortifying plant cell walls, to be more amenable to chemical depolymerization can lower the energy required for industrial processing. We have engineered poplar trees to introduce ester linkages into the lignin polymer backbone by augmenting the monomer pool with monolignol ferulate conjugates. Herein, we describe the isolation of a transferase gene capable of forming these conjugates and its xylem-specific introduction into poplar. Enzyme kinetics, in planta expression, lignin structural analysis, and improved cell wall digestibility after mild alkaline pretreatment demonstrate that these trees produce the monolignol ferulate conjugates, export them to the wall, and use them during lignification. Tailoring plants to use such conjugates during cell wall biosynthesis is a promising way to produce plants that are designed for deconstruction.
Subject(s)
Acyltransferases/chemistry , Acyltransferases/genetics , Lignin/chemistry , Lignin/metabolism , Populus/genetics , Populus/metabolism , Acyltransferases/isolation & purification , Angelica sinensis/enzymology , Angelica sinensis/genetics , Cell Wall/chemistry , Cell Wall/metabolism , Coumaric Acids/metabolism , Genes, Plant , Molecular Structure , Plant Roots/enzymology , Plants, Genetically Modified/genetics , Plants, Genetically Modified/growth & development , Populus/growth & development , Trees/genetics , Trees/metabolismABSTRACT
Molecular nanostructures may constitute the fabric of future quantum technologies, if their degrees of freedom can be fully harnessed. Ideally one might use nuclear spins as low-decoherence qubits and optical excitations for fast controllable interactions. Here, we present a method for entangling two nuclear spins through their mutual coupling to a transient optically excited electron spin, and investigate its feasibility through density-functional theory and experiments on a test molecule. From our calculations we identify the specific molecular properties that permit high entangling power gates under simple optical and microwave pulses; synthesis of such molecules is possible with established techniques.