4.7 Article

Characterization, Expression Profiling, and Biochemical Analyses of the Cinnamoyl-CoA Reductase Gene Family for Lignin Synthesis in Alfalfa Plants

期刊

出版社

MDPI
DOI: 10.3390/ijms23147762

关键词

cinnamoyl-CoA reductase; kinetic analysis; lignin biosynthesis; Medicago sativa

资金

  1. National Natural Science Foundation of China [31871545]

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In this study, the characteristics, gene expression, and substrate-binding motif of the Cinnamoyl-CoA reductase (CCR) gene family in alfalfa were investigated. The results suggest that CCR plays a pivotal role in lignin synthesis and plant development, as well as in response to environmental stresses. These findings have important implications for improving legume forage quality and biofuels industry engineering in the future.
Cinnamoyl-CoA reductase (CCR) is a pivotal enzyme in plant lignin synthesis, which has a role in plant secondary cell wall development and environmental stress defense. Alfalfa is a predominant legume forage with excellent quality, but the lignin content negatively affects fodder digestibility. Currently, there is limited information on CCR characteristics, gene expression, and its role in lignin metabolism in alfalfa. In this study, we identified 30 members in the CCR gene family of Medicago sativa. In addition, gene structure, conserved motif, and evolution analysis suggested MsCCR1-7 presumably functioned as CCR, while the 23 MsCCR-likes fell into three categories. The expression patterns of MsCCRs/MsCCR-likes suggested their role in plant development, response to environmental stresses, and phytohormone treatment. These results were consistent with the cis-elements in their promoters. Histochemical staining showed that lignin accumulation gradually deepened with the development, which was consistent with gene expression results. Furthermore, recombinant MsCCR1 and MsCCR-like1 were purified and the kinetic parameters were tested under four substrates. In addition, three-dimensional structure models of MsCCR1 and MsCCR-like1 proteins showed the difference in the substrate-binding motif H212(X)2K215R263. These results will be useful for further application for legume forage quality modification and biofuels industry engineering in the future.

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