Lalehvash Moghaddam

Trehalose Accumulation Triggers Autophagy during Plant Desiccation

Global climate change, increasingly erratic weather and a burgeoning global population are significant threats to the sustainability of future crop production. There is an urgent need for the development of robust measures that enable crops to withstand the uncertainty of climate change whilst still producing maximum yields. Resurrection plants possess the unique ability to withstand desiccation for prolonged periods, can be restored upon watering and represent great potential for the development of stress tolerant crops. Here, we describe the remarkable stress characteristics of Tripogon loliiformis, an uncharacterised resurrection grass and close relative of the economically important cereals, rice, sorghum, and maize. We show that T. loliiformis survives extreme environmental stress by implementing autophagy to prevent Programmed Cell Death. Notably, we identified a novel role for trehalose in the regulation of autophagy in T.loliiformis. Transcriptome, Gas Chromatography Mass Spectrometry, immunoblotting and confocal microscopy analyses directly linked the accumulation of trehalose with the onset of autophagy in dehydrating and desiccated T. loliiformis shoots. These results were supported in vitro with the observation of autophagosomes in trehalose treated T. loliiformis leaves; autophagosomes were not detected in untreated samples. Presumably, once induced, autophagy promotes desiccation tolerance in T.loliiformis, by removal of cellular toxins to suppress programmed cell death and the recycling of nutrients to delay the onset of senescence. These findings illustrate how resurrection plants manipulate sugar metabolism to promote desiccation tolerance and may provide candidate genes that are potentially useful for the development of stress tolerant crops.

Effects of mesostructured silica catalysts on the depolymerization of organosolv lignin fractionated from woody eucalyptus

Isolated and purified organosolv eucalyptus wood lignin was depolymerized at different temperatures with and without mesostructured silica catalysts (i.e., SBA-15, MCM-41, ZrO2-SBA-15 and ZrO2-MCM-41). It was found that at 300°C for 1h with a solid/liquid ratio of 0.0175/1 (w/v), the SBA-15 catalyst with high acidity gave the highest syringol yield of 23.0% in a methanol/water mixture (50/50, wt/wt). Doping with ZrO2 over these catalysts did not increase syringol yield, but increased the total amount of solid residue. Gas chromatography-mass spectrometry (GC-MS) also identified other main phenolic compounds such as 1-(4-hydroxy-3,5-dimethoxyphenyl)-ethanone, 1,2-benzenediol, and 4-hydroxy-3,5-dimethoxy-benzaldehyde. Analysis of the lignin residues with Fourier transform-infrared spectroscopy (FT-IR) indicated decreases in the absorption bands intensities of OH group, CO stretching of syringyl ring and aromatic CH deformation of syringol unit, and an increase in band intensities associated with the guaiacyl ring, confirming the type of products formed.

Effects of an alkali-acid purification process on the characteristics of eucalyptus lignin fractionated from a MIBK-based organosolv process

In this study, the effects of an alkali-acid purification process on the properties of eucalyptus lignin isolated from a methyl isobutyl ketone (MIBK)/methanol/water-based organosolv fractionation process were evaluated. The results showed that the treatment reduced the content of carbohydrates, ash, nitrogen and sulfur, and improved lignin solubility (up to 218%) in five organic solvents (acetone, methanol, ethanol, tetrahydrofuran and dimethyl sulfoxide) and removed lignin fractions with smaller molecular weights. However, analysis by Py-GC/MS, solid state NMR and 2D-HSQC NMR indicated that the alkali-acid treatment process did not cause changes to the monomeric lignin subunits and linkages of the lignin polymer. The treated lignin showed slightly higher thermal stability at temperatures <250 °C, though its maximum rate of decomposition occurred at 325 °C, 26 °C lower than that of the untreated lignin. On the basis of these results, the significant improvement in solvent solubility of the lignin by the treatment process will widen lignin application.

Co- and Ca-phosphate-based catalysts for the depolymerization of organosolv eucalyptus lignin

Depolymerization of purified organosolv eucalyptus wood lignin by heterogeneous catalysts, cobalt polyphosphate (CoP2O6) and calcium phosphate (β-CaP2O6) was investigated. A total syringol yield of 16.7% was achieved with β-CaP2O6 in a methanol–water (50/50, w/w) solvent system after depolymerization at 300 °C for 1 h, showing the selectivity of the catalyst.

Calcium Phosphate Flocs and the Clarification of Sugar Cane Juice from Whole of Crop Harvesting

Sugar cane biomass is one of the most viable feedstocks for the production of renewable fuels and chemicals. Therefore, processing the whole of crop (WC) (i.e., stalk and trash, instead of stalk only) will increase the amount of available biomass for this purpose. However, effective clarification of juice expressed from WC for raw sugar manufacture is a major challenge because of the amounts and types of non-sucrose impurities (e.g., polysaccharides, inorganics, proteins, etc.) present. Calcium phosphate flocs are important during sugar cane juice clarification because they are responsible for the removal of impurities. Therefore, to gain a better understanding of the role of calcium phosphate flocs during the juice clarification process, the effects of impurities on the physicochemical properties of calcium phosphate flocs were examined using small-angle laser light scattering technique, attenuated total reflectance Fourier transformed infrared spectroscopy, and X-ray powder diffraction. Results on synthetic sugar juice solutions showed that the presence of SiO2 and Na(+) ions affected floc size and floc structure. Starch and phosphate ions did not affect the floc structure; however, the former reduced the floc size, whereas the latter increased the floc size. The study revealed that high levels of Na(+) ions would negatively affect the clarification process the most, as they would reduce the amount of suspended particles trapped by the flocs. A complementary study on prepared WC juice using cold and cold/intermediate liming techniques was conducted. The study demonstrated that, in comparison to the one-stage (i.e., conventional) clarification process, a two-stage clarification process using cold liming removed more polysaccharides (≤19%), proteins (≤82%), phosphorus (≤53%), and SiO2 (≤23%) in WC juice but increased Ca(2+) (≤136%) and sulfur (≤200%).

Degradation of phenethoxybenzene in sodium hydroxide

Simple lignin model compounds containing β-O-4 aryl ether linkages have been utilized as a means to understand lignin depolymerisation. The effects of reaction temperature, time, catalyst concentration, and initial phenethoxybenzene (PEB) concentration on the degradation of PEB in NaOH were investigated. Operating at 300 °C for 1 h resulted in the highest combined yield of the primary products, phenol and styrene, and also resulted in a reduced amount of degradation products formed. The proportion of oligomeric and polymeric materials formed depended on the NaOH concentration, but not on the initial PEB concentration for equal reaction time. The results were used to suggest probable reaction pathways for PEB degradation.