4.8 Article

Disruption of Brachypodium lichenase alters metabolism of mixed-linkage glucan and starch

期刊

PLANT JOURNAL
卷 109, 期 4, 页码 927-939

出版社

WILEY
DOI: 10.1111/tpj.15603

关键词

mixed-linkage glucan; lichenase; BdLCH1; chlorenchyma cells; starch; Brachypodium distachyon

资金

  1. Great Lakes Bioenergy Research Center, U.S. Department of Energy, Office of Science, Office of Biological and Environmental Research [DE-SC0018409]

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The study identifies a gene encoding a lichenase BdLCH1 in Brachypodium distachyon, which is highly expressed in the endosperm of germinating seeds and chlorenchyma cells of mature leaves. Disruption of BdLCH1 leads to increased mixed-linkage glucan content in senesced leaves, suggesting a role in cell wall modification to support highly metabolically active cells.
Mixed-linkage glucan, which is widely distributed in grasses, is a polysaccharide highly abundant in cell walls of grass endosperm and young vegetative tissues. Lichenases are enzymes that hydrolyze mixed-linkage glucan first identified in mixed-linkage glucan-rich lichens. In this study, we identify a gene encoding a lichenase we name Brachypodium distachyon LICHENASE 1 (BdLCH1), which is highly expressed in the endosperm of germinating seeds and coleoptiles and at lower amounts in mature shoots. RNA in situ hybridization showed that BdLCH1 is primarily expressed in chlorenchyma cells of mature leaves and internodes. Disruption of BdLCH1 resulted in an eight-fold increase in mixed-linkage glucan content in senesced leaves. Consistent with the in situ hybridization data, immunolocalization results showed that mixed-linkage glucan was not removed in chlorenchyma cells of lch1 mutants as it was in wild type and implicate the BdLCH1 enzyme in removing mixed-linkage glucan in chlorenchyma cells in mature vegetative tissues. We also show that mixed-linkage glucan accumulation in lch1 mutants was resistant to dark-induced degradation, and 8-week-old lch1 plants showed a faster rate of starch breakdown than wild type in darkness. Our results suggest a role for BdLCH1 in modifying the cell wall to support highly metabolically active cells.

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