Plants use sunlight and water to capture CO2 from the atmosphere to build their biomass. That biomass can then be converted to products that are nowadays made from fossil resources such as petroleum. Whereas the use of fossil resources leads to a net increase of CO2 into the atmosphere (e.g. when burning it as fuel), this is not the case when using plant biomass. For this reason, plant biomass is considered a renewable, carbon-neutral resource. 

A major objective of the group is to demonstrate, in field trials, that the improved biomass processing efficiency of the engineered, greenhouse-grown biomass crops is maintained when plants are grown in the field. This is especially relevant for poplar, as trees are harvested in winter when leaves have been shed and the wood formation program has ended. But also for maize, plants grown in the field are phenotypically very different from those grown in the greenhouse due to the very different environment.

A main bottleneck in our gene discovery studies is that the identity of most metabolites is unknown. We can only understand the response to pathway perturbations, when we know the identity of the differentially accumulating compounds, e.g. in reverse genetics studies where we aim at identifying the substrate for an enzyme.

A second plausible cause of the observed phenotypic consequences of lignin-modified plants is the differential accumulation of soluble bioactive phenolics in the lignin-modified plants compared to the wild type.

In addition to engineering lignin structure by using genes of the host plant itself (modification of H/G/S/benzodioxanes/aldehydes/ferulates levels; Chanoca et al., 2019), it is also possible to engineer easily degradable lignin polymers by using genes from other taxa in a synthetic biology approach, as discussed in Vanholme et al. (2012).

Engineering plants for reduced lignin amount or altered structure is often associated with a yield penalty. Several hypotheses have been put forward to explain the molecular basis of the yield penalty. It has been shown that lignin modification often results in a collapse of vessels, which negatively affects water and nutrient transport in the plant.

When improving plant cell walls, it all comes down to identifying the genes that are involved in the biosynthesis of the major cell wall polymers, and altering their expression levels in target crops such as poplar and maize. Through co-expression analyses in Arabidopsis and maize, we have identified a set of candidate genes that likely play an important role in phenolic biosynthesis.