Sucrose Utilization for Improved Crop Yields: A Review Article

Photosynthetic carbon converted to sucrose is vital for plant growth. Sucrose acts as a signaling molecule and a primary energy source that coordinates the source and sink development. Alteration in source–sink balance halts the physiological and developmental processes of plants, since plant growth is mostly triggered when the primary assimilates in the source leaf balance with the metabolic needs of the heterotrophic sinks. To measure up with the sink organ’s metabolic needs, the improvement of photosynthetic carbon to synthesis sucrose, its remobilization, and utilization at the sink level becomes imperative. However, environmental cues that influence sucrose balance within these plant organs, limiting positive yield prospects, have also been a rising issue over the past few decades. Thus, this review discusses strategies to improve photosynthetic carbon assimilation, the pathways actively involved in the transport of sucrose from source to sink organs, and their utilization at the sink organ. We further emphasize the impact of various environmental cues on sucrose transport and utilization, and the strategic yield improvement approaches under such conditions.

Potassium Application Boosts Photosynthesis and Sorbitol Biosynthesis and Accelerates Cold Acclimation of Common Plantain (Plantago major L.)

Potassium (K) is essential for the processes critical for plant performance, including photosynthesis, carbon assimilation, and response to stress. K also influences translocation of sugars in the phloem and regulates sucrose metabolism. Several plant species synthesize polyols and transport these sugar alcohols from source to sink tissues. Limited knowledge exists about the involvement of K in the above processes in polyol-translocating plants. We, therefore, studied K effects in Plantago major, a species that accumulates the polyol sorbitol to high concentrations. We grew P. major plants on soil substrate adjusted to low-, medium-, or high-potassium conditions. We found that biomass, seed yield, and leaf tissue K contents increased in a soil K-dependent manner. K gradually increased the photosynthetic efficiency and decreased the non-photochemical quenching. Concomitantly, sorbitol levels and sorbitol to sucrose ratio in leaves and phloem sap increased in a K-dependent manner. K supply also fostered plant cold acclimation. High soil K levels mitigated loss of water from leaves in the cold and supported cold-dependent sugar and sorbitol accumulation. We hypothesize that with increased K nutrition, P. major preferentially channels photosynthesis-derived electrons into sorbitol biosynthesis and that this increased sorbitol is supportive for sink development and as a protective solute, during abiotic stress.

Enhancing biomass production and yield by maintaining enhanced capacity for CO2 uptake in response to elevated CO2

Dahal, K., Weraduwage, S. M., Kane, K., Rauf, S. A., Leonardos, E. D., Gadapati, W., Savitch, L., Singh, J., Marillia, E.-F., Taylor, D. C., Micallef, M. C., Knowles, V., Plaxton, W., Barron, J., Sarhan, F., Hüner, N., Grodzinski, B. and Micallef, B. J. 2014. Enhancing biomass production and yield by maintaining enhanced capacity for CO2 uptake in response to elevated CO2. Can. J. Plant Sci. 94: 1075–1083. Using four model plants, two members of the Gramineae, rye and wheat, and two Brassicaceae, Brassica napus and Arabidopsis thaliana, two fundamental approaches were exploited to determine how regulating source-sink development would alter photosynthesis, productivity and yield during long-term acclimation to elevated CO2. In one approach we exploited the cold acclimation response of winter wheat, rye and B. napus. In the other approach we modified the dark respiration in A. thaliana to alter availability of respiratory substrates required for anabolic processes, such as fatty acid metabolism, thus reducing sink limitations on canopy photosynthesis at elevated CO2. Taken together, the data show the importance of maintaining strong demand from active sinks when the above-ground canopy is being exposed to elevated levels of the primary substrate of photosynthesis, CO2.

A bonding process between grains in mechanically disaggregated snow

Collections of disaggregated snow particles were examined in a temperature-controlled microscope stage. In addition to necks that appeared to sinter in a manner congruent with the two-particle model, there also appeared unanticipated dendritic growth, which developed on some grains and grew into the pore space. These branches developed preferentially only on part of, and in different directions on, individual grains. Some of these grew enough to join with adjacent grains that were in close proximity but not initially in contact, while the surface of the adjacent grains did not show measurable growth or loss. Growth orientation is hypothesized to be due to crystal habit dependence on temperature. Columnar growth was observed at –5˚C and plate-like at –15˚C. The random growth orientation is in contrast to observed source and sink development aligned with a temperature gradient imposed using a gradient stage. In this case, a source-to-sink directionality across the pore was apparent in which faceted crystals grew at the expense of neighboring source grains. The process of mechanically disaggregating snow produces numerous broken shards and sharp-edged fracture surfaces. We hypothesize that it is the sublimation of these high-surface-energy regions that provides the excess vapor to facilitate the diffusion-limited dendritic growth observed in this ‘equitemperature’, mechanically processed snow.

Interactions Between Rising CO2 Concentration and Nitrogen Supply in Cotton. I. Growth and Leaf Nitrogen Concentration

The influence of sink development on the response of shoot growth in cotton (Gossypium hirsutum L. cv. Siokra BT1-4) was investigated by growing plants at three levels of CO2=2 concentration: 350 (ambient), 550 and 900 μL L-1 and six levels of nitrogen (N) supply ranging from deficient to excess (0-133 mg N kg-1 soil week-1). Changes in leaf N concentration were also investigated. At 59 days after sowing, there was an average 63% increase in shoot growth at 550 μL CO2 L-1 compared with ambient CO2-grown plants, with no significant growth increase at 900 μL CO2 L-1 and, this response was closely matched by sink development (flower number and stem weight). Low N supply restricted the responses of both sink development and shoot growth to high CO2. At elevated CO2, leaf N concentration was reduced by an average 27% at low to adequate N supply. The high CO2-induced reduction in leaf N concentration, however, disappeared when the N supply was increased to a high level of 133 mg N kg-1 soil week-1. These CO2 effects on leaf N concentration were smaller when N was expressed per unit leaf area, apparently due to a combination of the effects of elevated CO2 or high N supply reducing specific leaf area and, to an N uptake limitation at low to moderate levels of N supply. The critical foliar N concentrations (leaf N concentration at 90% of maximum shoot growth) were reduced from 42 to 38 and 36 mg g-1 when CO2 concentrations were increased from 350 to 550 and 900 μL L-1 respectively, indicating that changes in fertiliser management may be required under changing CO2 concentrations.