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Rice calli may decelerate its metabolism to adapt hormone free medium

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Abstract

This report focuses on the crucial role of lipids and starch metabolism in the growth and ultrastructure of the cell wall (CW) in rice calli. Non-habituated calli (NH-calli) were isolated from a rice embryo-derived callus culture supplemented with 2,4-D (2,4-Dichlorophenoxyacetic acid); however, the habituated calli (H-calli) were isolated from NH ones and cultured subsequently on exogenous hormone-free medium. The phenotypes of the H- and NH-calli differed significantly between each other as reported in our recently published work. The H-calli CW was thinner, the endoplasmic reticulum (ER), mitochondria (MT) and starch grains (SGs) were less in the H-calli. The intracellular free fatty acids (FAs) and starch content were much less in the H- if compared to NH-calli. By microarray analysis, the differentially expressed genes (DEGs) related to primary and secondary metabolism, lipid and starch metabolism were down-regulated in H- vs NH-calli. The response at the transcriptomic level involved in these changes, as well as the corresponding variations in cytology and FAs metabolism were also accurately elucidated herein. The study reveals that the decreased levels of lipids and starch in the H-calli are mainly attributable to their (H-calli) elevated consumption, in the absence of exogenous hormonal supply to ensure the demand in energy of the calli to survive and maintain an optimum growth and development with the available resource of energy (starch and lipids). This report displays as well the slowdown of the H-calli metabolism, in the absence of exogenous growth regulators supply, if compared to that of the NH-ones.

Key message

Lipids and starch decreased in the H-calli is mainly attributable to their elevated consumption to survive and maintain an optimal growth and development with the available resource of energy.

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This study includes two supplemental tables.

Abbreviations

ACBP:

acyl-CoA-binding protein

ACS:

acyl-CoA synthetase

CW:

cell wall

Cryo-SEM:

Cryo-scanning electron microscopy

DAG:

1,3-diacylglycerol

DEGs:

differentially expressed genes

DGAT:

diacylglycerol O-acyltransferase

d:

day

FAs:

fatty acids

FAE:

fatty acid elongase

FAR:

fatty acyl-CoA reductase

FM:

Fluorescence microscopy

KCS:

3-ketoacyl-CoA synthase

LD:

lipid drop

LM:

light microscopy

LTPs:

lipid transfer proteins

PM:

plasmalemma

qRT-PCR:

Quantitative real-time polymerase chain reaction

TAG:

triacylglycerol

TEM:

Transmission electron microscopy

2,4-D:

2,4-Dichlorophenoxyacetic acid.

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Acknowledgements

The authors thank Wenli Hu (Center for Excellence in Molecular Plant Sciences, Shanghai Institute of Plant Physiology and Ecology, Chinese Academy of Sciences) for assistance with the GC-MS analysis; and Xiaoyan Gao, Jiqin Li and Zhiping Zhang (Center for Excellence in Molecular Plant Sciences, Shanghai Institute of Plant Physiology and Ecology, Chinese Academy of Sciences) for assistance with the cryo-SEM and TEM analyses.

Funding

This work was supported by the funding from the national natural science foundation of China, NSFC (Grant Nos. 31600684, U1738107, 31570859 and 31370214).

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Contributions

All authors contributed to the study conception and design. Material preparation and experiment conduction were performed by J.J. and J.D.. Data collection and analysis were performed by J.J., J.Z., J.E. and W.C.. The first draft of the manuscript was written by J.J. and edited by J.E.. All authors commented on previous versions of the manuscript. All authors read and approved the final manuscript.

Corresponding authors

Correspondence to Jian Zhu or Weiming Cai.

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The authors declare that they have no conflict of interest.

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Communicated by Manoj Prasad.

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Jin, J., Essemine, J., Duan, J. et al. Rice calli may decelerate its metabolism to adapt hormone free medium. Plant Cell Tiss Organ Cult 145, 223–238 (2021). https://doi.org/10.1007/s11240-020-02004-z

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  • DOI: https://doi.org/10.1007/s11240-020-02004-z

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