4.8 Article

BETA-AMYLASE9 is a plastidial nonenzymatic regulator of leaf starch degradation

Journal

PLANT PHYSIOLOGY
Volume 188, Issue 1, Pages 191-207

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1093/plphys/kiab468

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Funding

  1. ETH Zurich
  2. Korea Research Foundation - Korean Government (MOEHRD, Basic Research Promotion Fund) [KRF-2008C00143]

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Beta-amylases (BAMs) play a crucial role in transitory starch degradation in chloroplasts, regulating the availability of photosynthetically fixed carbon over the diel cycle in plants. The characterization of BETA-AMYLASE 9 (BAM9) in Arabidopsis revealed its conservation in plants and unique regulation of starch breakdown compared to BAM4. BAM9 activates starch degradation and responds to environmental changes, making it a valuable gene target for managing carbohydrate availability in fluctuating conditions.
beta-Amylases (BAMs) are key enzymes of transitory starch degradation in chloroplasts, a process that buffers the availability of photosynthetically fixed carbon over the diel cycle to maintain energy levels and plant growth at night. However, during vascular plant evolution, the BAM gene family diversified, giving rise to isoforms with different compartmentation and biological activities. Here, we characterized BETA-AMYLASE 9 (BAM9) of Arabidopsis (Arabidopsis thaliana). Among the BAMs, BAM9 is most closely related to BAM4 but is more widely conserved in plants. BAM9 and BAM4 share features including their plastidial localization and lack of measurable alpha-1,4-glucan hydrolyzing capacity. BAM4 is a regulator of starch degradation, and bam4 mutants display a starch-excess phenotype. Although bam9 single mutants resemble the wild-type (WT), genetic experiments reveal that the loss of BAM9 markedly enhances the starch-excess phenotypes of mutants already impaired in starch degradation. Thus, BAM9 also regulates starch breakdown, but in a different way. Interestingly, BAM9 gene expression is responsive to several environmental changes, while that of BAM4 is not. Furthermore, overexpression of BAM9 in the WT reduced leaf starch content, but overexpression in bam4 failed to complement fully that mutant's starch-excess phenotype, suggesting that BAM9 and BAM4 are not redundant. We propose that BAM9 activates starch degradation, helping to manage carbohydrate availability in response to fluctuations in environmental conditions. As such, BAM9 represents an interesting gene target to explore in crop species.

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