Abstract
BackgroundOne-carbon (C1) metabolism is important for synthesizing a range of biologically important compounds that are essential for life. In plants, the C1 pathway is crucial for the synthesis of a large number of secondary metabolites, including lignin. Tetrahydrofolate and its derivatives, collectively referred to as folates, are crucial co-factors for C1 metabolic pathway enzymes. Given the link between the C1 and phenylpropanoid pathways, we evaluated whether folylpolyglutamate synthetase (FPGS), an enzyme that catalyzes the addition of a glutamate tail to folates to form folylpolyglutamates, can be a viable target for reducing cell wall recalcitrance in plants.ResultsConsistent with its role in lignocellulosic formation, FPGS1 was preferentially expressed in vascular tissues. Total lignin was low in fpgs1 plants leading to higher saccharification efficiency of the mutant. The decrease in total lignin in fpgs1 was mainly due to lower guaiacyl (G) lignin levels. Glycome profiling revealed subtle alterations in the cell walls of fpgs1. Further analyses of hemicellulosic polysaccharides by NMR showed that the degree of methylation of 4-O-methyl glucuronoxylan was reduced in the fpgs1 mutant. Microarray analysis and real-time qRT-PCR revealed that transcripts of a number of genes in the C1 and lignin pathways had altered expression in fpgs1 mutants. Consistent with the transcript changes of C1-related genes, a significant reduction in S-adenosyl-l-methionine content was detected in the fpgs1 mutant. The modified expression of the various methyltransferases and lignin-related genes indicate possible feedback regulation of C1 pathway-mediated lignin biosynthesis.ConclusionsOur observations provide genetic and biochemical support for the importance of folylpolyglutamates in the lignocellulosic pathway and reinforces previous observations that targeting a single FPGS isoform for down-regulation leads to reduced lignin in plants. Because fpgs1 mutants had no dramatic defects in above ground biomass, selective down-regulation of individual components of C1 metabolism is an approach that should be explored further for the improvement of lignocellulosic feedstocks.Electronic supplementary materialThe online version of this article (doi:10.1186/s13068-015-0403-z) contains supplementary material, which is available to authorized users.
Highlights
One-carbon (C1) metabolism is important for synthesizing a range of biologically important compounds that are essential for life
Methionine is an important product of the C1 metabolic pathway because it is the direct precursor of S-adenosyl l-methionine (AdoMet), the universal methyl-group donor, which is crucial for the synthesis of a large number of secondary metabolites [3], such as lignin, betaines, phytohormones [4], and hemicellulosic 4-O-methyl glucuronoxylan (GX) [5]
FPGS1 is preferentially expressed in vascular tissues, consistent with its role in lignin biosynthesis Lignification in plants occurs predominantly in the vascular tissues where secondary cell walls are formed
Summary
One-carbon (C1) metabolism is important for synthesizing a range of biologically important compounds that are essential for life. The C1 pathway is crucial for the synthesis of a large number of secondary metabolites, including lignin. Tetrahydrofolate and its derivatives, collectively referred to as folates, are crucial co-factors for C1 metabolic pathway enzymes. Given the link between the C1 and phenylpropanoid pathways, we evaluated whether folylpolyglutamate synthetase (FPGS), an enzyme that catalyzes the addition of a glutamate tail to folates to form folylpolyglutamates, can be a viable target for reducing cell wall recalcitrance in plants. Methionine is an important product of the C1 metabolic pathway because it is the direct precursor of S-adenosyl l-methionine (AdoMet), the universal methyl-group donor, which is crucial for the synthesis of a large number of secondary metabolites [3], such as lignin, betaines, phytohormones [4], and hemicellulosic 4-O-methyl glucuronoxylan (GX) [5]. Interaction of lignin with other wall matrix components has become a focus of cell wall research [13]
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