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PreprintCC BY-NC-NDbioRxiv

ZmPMI3 phosphomannose isomerase kinetics is associated with natural variation of watersoluble carbohydrate content in mature maize stem

  1. 1Heinrich Heine University Duesseldorf, Institute for Plant Cell Biology and Biotechnology

Abstract

Mature maize stems accumulate substantial amounts of water-soluble carbohydrates (WSC) providing an accessible carbon pool for industrial bioconversion. However, the genetic factors controlling WSC reserves under field conditions remain poorly resolved. In this study, we quantified total WSC including glucose, fructose, sucrose contents in the internode below the first ear of a genetically diverse maize panel at physiological maturity and associated trait variation with genome-wide SNP data. The panel displayed extensive variation in stem WSCs content, with values ranging up to 50.4 % of dry weight. Genome-wide association mapping identified 20 quantitative trait loci associated with individual sugars or total WSC content. One fructose associated region contained two adjacent gene annotations predicted to encode fragments of a phosphomannose isomerase. Sequence comparison, cDNA amplification and protein structure prediction supported a unified gene model, here designated as ZmPMI3. Biochemical characterization showed ZmPMI3 catalyzes the reversible conversion between mannose-6-phosphate and fructose-6-phosphate, a central reaction in carbohydrate metabolism. Natural protein haplotypes with distinct kinetic properties were identified correlating with significant differences in stem WSC content. Together, these findings identify ZmPMI3 as a candidate contributor to natural variation in maize stem carbohydrate reserves, potentially through altered hexose-phosphate partitioning.

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BibTeX
@misc{robertz2026zmpmi3,
  title = {{ZmPMI3 phosphomannose isomerase kinetics is associated with natural variation of watersoluble carbohydrate content in mature maize stem}},
  author = {S. Robertz and S. Wang and F. Roeber and S. Groh and M. Pauly and V. Ramirez},
  howpublished = {bioRxiv},
  year = {2026},
  month = oct,
  doi = {10.64898/2026.10.12.758442},
  url = {https://www.biorxiv.org/content/10.64898/2026.10.12.758442v1},
  note = {CC BY-NC-ND},
}
RIS
TY  - UNPB
TI  - ZmPMI3 phosphomannose isomerase kinetics is associated with natural variation of watersoluble carbohydrate content in mature maize stem
AU  - S. Robertz
AU  - S. Wang
AU  - F. Roeber
AU  - S. Groh
AU  - M. Pauly
AU  - V. Ramirez
PY  - 2026
DA  - 2026/10/12
PB  - bioRxiv
DO  - 10.64898/2026.10.12.758442
UR  - https://www.biorxiv.org/content/10.64898/2026.10.12.758442v1
AB  - Mature maize stems accumulate substantial amounts of water-soluble carbohydrates (WSC) providing an accessible carbon pool for industrial bioconversion. However, the genetic factors controlling WSC reserves under field conditions remain poorly resolved. In this study, we quantified total WSC including glucose, fructose, sucrose contents in the internode below the first ear of a genetically diverse maize panel at physiological maturity and associated trait variation with genome-wide SNP data. The panel displayed extensive variation in stem WSCs content, with values ranging up to 50.4 % of dry weight. Genome-wide association mapping identified 20 quantitative trait loci associated with individual sugars or total WSC content. One fructose associated region contained two adjacent gene annotations predicted to encode fragments of a phosphomannose isomerase. Sequence comparison, cDNA amplification and protein structure prediction supported a unified gene model, here designated as ZmPMI3. Biochemical characterization showed ZmPMI3 catalyzes the reversible conversion between mannose-6-phosphate and fructose-6-phosphate, a central reaction in carbohydrate metabolism. Natural protein haplotypes with distinct kinetic properties were identified correlating with significant differences in stem WSC content. Together, these findings identify ZmPMI3 as a candidate contributor to natural variation in maize stem carbohydrate reserves, potentially through altered hexose-phosphate partitioning.
ER  -