Class III peroxidases in cellulose deficient cultured maize cells during cell wall remodeling.


Journal article


Romina Martínez-Rubio, J. Acebes, A. Encina, A. Kärkönen
Physiologia Plantarum : An International Journal for Plant Biology, 2018

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APA   Click to copy
Martínez-Rubio, R., Acebes, J., Encina, A., & Kärkönen, A. (2018). Class III peroxidases in cellulose deficient cultured maize cells during cell wall remodeling. Physiologia Plantarum : An International Journal for Plant Biology.


Chicago/Turabian   Click to copy
Martínez-Rubio, Romina, J. Acebes, A. Encina, and A. Kärkönen. “Class III Peroxidases in Cellulose Deficient Cultured Maize Cells during Cell Wall Remodeling.” Physiologia Plantarum : An International Journal for Plant Biology (2018).


MLA   Click to copy
Martínez-Rubio, Romina, et al. “Class III Peroxidases in Cellulose Deficient Cultured Maize Cells during Cell Wall Remodeling.” Physiologia Plantarum : An International Journal for Plant Biology, 2018.


BibTeX   Click to copy

@article{romina2018a,
  title = {Class III peroxidases in cellulose deficient cultured maize cells during cell wall remodeling.},
  year = {2018},
  journal = {Physiologia Plantarum : An International Journal for Plant Biology},
  author = {Martínez-Rubio, Romina and Acebes, J. and Encina, A. and Kärkönen, A.}
}

Abstract

Maize (Zea mays L.) suspension-cultured cells habituated to a cellulose biosynthesis inhibitor 2,6-dichlorobenzonitrile (DCB) have a modified cell wall, in which the reduction in the cellulose content is compensated by a network of highly cross-linked feruloylated arabinoxylans and the deposition of lignin-like polymers. For both arabinoxylan cross-linking and lignin polymerization, class III peroxidases (POXs) have been demonstrated to have a prominent role. For the first time, a comparative study of POX activity and isoforms in control and cellulose-impaired cells has been addressed, also taking into account their cellular distribution in different compartments. Proteins from the spent medium (SM), soluble cellular (SC), ionically (ICW) and covalently bound cell wall protein fractions were assayed for total and specific peroxidase activity by using coniferyl and sinapyl alcohol and ferulic acid as substrates. The isoPOX profile was obtained by isoelectric focusing. POX activity was higher in DCB-habituated than in non-habituated cells in all protein fractions at all cell culture stages. For all substrates assayed, SC and ICW fractions showed higher activity at the early log growth phase than at the late log phase. However, the highest POX activity in the spent medium was found at the late log phase. According to the isoPOX profiles, the highest diversity of isoPOXs was detected in the ICW and SM protein fractions. The latter fraction contained isoPOXs with higher activity in DCB-habituated cells. Some of the isoPOXs detected could be involved in cross-linking of arabinoxylans and in the lignin-like polymer formation in DCB-habituated cells.