METABOLIC CHANNELING OF PHE FOR LIGNIN
BIOSYNTHESIS IN MARITIME PINE
Jorge El-Azaz, Fernando de la Torre, Belén Pascual,
Concepción Ávila and Francisco M. Cánovas
Departamento de Biología Molecular y Bioquímica, Universidad de Málaga.
Málaga, Spain
Email: jelazaz@alu.uma.es
The amino acid phenylalanine (Phe) is the main precursor of
phenylpropanoids biosynthesis in plants. This vast family of Phederived
compounds can represent up to 30% of captured
photosynthetic carbon, playing essential roles in plants such as cell
wall components, defense molecules, pigments and flavors. In
addition to its physiological importance, phenylpropanoids and
particularly lignin, a component of wood, are targets in plant
biotechnology.
The arogenate pathway has been proposed as the main pathway for
Phe biosynthesis in plants (Maeda et al., 2010). The final step in Phe
biosynthesis, catalyzed by the enzyme arogenate dehydratase (ADT),
has been considered as a key regulatory point in Phe biosynthesis,
due to its key branch position in the pathway, the multiple
isoenzymes identified in plants and the existence of a feedback
inhibition mechanism by Phe. So far, the regulatory mechanisms
underlying ADT genes expression have been poorly characterized,
although a strong regulation of the Phe metabolic flux should be
expected depending on its alternative use for protein biosynthesis
versus phenylpropanoid biosynthesis. This second fate involves a
massive carbon flux compared to the first one.
In this study we report our current research activities in the
transcriptional regulation of ADT genes by MYB transcription factors
in the conifer Pinus pinaster (maritime pine). The conifers channels
massive amounts of photosynthetic carbon for phenylpropanoid
biosynthesis during wood formation. We have identified the
complete ADT gene family in maritime pine (El-Azaz et al., 2016)
and a set of ADT isoforms specifically related with the lignification
process. The potential control of transcription factors previously
reported as key regulators in pine wood formation (Craven-Bartle et
al., 2013) will be presented.
Maeda et al. (2010) Plant Cell 22: 832-849.
El-Azaz et al. (2016) The Plant Jounal. Accepted article, doi:
10.1111/tpj.13195
Craven-Bartle et al. (2013). The Plant Journal 74(5):755-766