Abstract
Boron (B) is an essential microelement for higher plants, and its deficiency is widespread around the world and constrains the productivity of both agriculture and forestry. In the last two decades, numerous studies on model or herbaceous plants have contributed greatly to our understanding of the complex network of B-deficiency responses and mechanisms for tolerance. In woody plants, however, fewer studies have been conducted and they have not well been recently synthesized or related to the findings on model species on B transporters. Trees have a larger body size, longer lifespan and more B reserves than do herbaceous plants, indicating that woody species might undergo long-term or mild B deficiency more commonly and that regulation of B reserves helps trees cope with B deficiency. In addition, the highly heterozygous genetic background of tree species suggests that they may have more complex mechanisms of response and tolerance to B deficiency than do model plants. Boron-deficient trees usually exhibit two key visible symptoms: depression of growing points (root tip, bud, flower, and young leaf) and deformity of organs (root, shoot, leaf, and fruit). These symptoms may be ascribed to B functioning in the cell wall and membrane, and particularly to damage to vascular tissues and the suppression of both B and water transport. Boron deficiency also affects metabolic processes such as decreased leaf photosynthesis, and increased lignin and phenol content in trees. These negative effects will influence the quality and quantity of wood, fruit and other agricultural products. Boron efficiency probably originates from a combined effect of three processes: B uptake, B translocation and retranslocation, and B utilization. Root morphology and mycorrhiza can affect the B uptake efficiency of trees. During B translocation from the root to shoot, differences in B concentration between root cell sap and xylem exudate, as well as water use efficiency, may play key roles in tolerance to B deficiency. In addition, B retranslocation efficiency primarily depends on the extent of xylem-to-phloem transfer and the variety and amount of cis-diol moieties in the phloem. The B requirement for cell wall construction also contribute to the B use efficiency in trees. The present review will provide an update on the physiological and molecular responses and tolerance mechanisms to B deficiency in woody plants. Emphasis is placed on the roles of B reserves that are more important for tolerance to B deficiency in trees than in herbaceous plants and the possible physiological and molecular mechanisms of differential B efficiency in trees. We propose that B may be used to study the relationship between the cell wall and the membrane via the B-bridge. Transgenic B-efficient tree cultivars have considerable potential for forestry or fruit rootstock production on low B soils in the future.
Highlights
Boron (B) is essential for the growth and development of higher plants (Warington, 1923)
AtBOR2 is an efflux-type B transporter that is localized to the plasma membrane and has been proposed to facilitate the effective cross linking of rhamnogalacturonan II (RG-II) by B in the cell wall and root cell elongation
Miwa et al (2013) demonstrated that the proportion of cross-linked RG-II in Arabidopsis bor2-1 and bor2-2 mutants (∼42.5 and ∼45.7%) was significantly lower than that of both wild type (∼54.0%) and bor1-3 mutant (∼52.8%) plants under B limitation. These results may suggest that B transport by the AtBOR2 protein from the symplast to the apoplast may be required for the effective cross linking of RG-II in the cell wall under B deficiency
Summary
Boron (B) is essential for the growth and development of higher plants (Warington, 1923). A consistent observation reported is that B deficiency can increase vascular cross sectional areas in Norway spruce needle (Sutinen et al, 2006, 2007), pumelo leaf and fruit vascular tissues (Liu et al, 2013b), and sweet orange (Citrus sinensis) leaf veins (Yang et al, 2013) These results suggest that B deficiency can increase the size but weaken the function of vascular tissue in trees. Boron starvation first damages the integrity of the cell wall and membrane, disrupting the phenol metabolism-related enzyme systems, such as phenylalanine-ammonium lyase (PAL; Cakmak et al, 1995; Brown et al, 2002), and results in the accumulation of phenols and related alterations of lignin synthesis from phenol alcohols (Pilbeam and Kirkby, 1983; Yang et al, 2013; Zhou et al, 2015). The accumulation of soluble sugars in B-deficient leaves of trees may produce feedback inhibition to net photosynthesis (Han et al, 2008; Ruuhola et al, 2011; Hajiboland et al, 2013b; Lu et al, 2014)
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