4.6 Article

Sugarcane Root Transcriptome Analysis Revealed the Role of Plant Hormones in the Colonization of an Endophytic Diazotroph

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FRONTIERS IN MICROBIOLOGY
卷 13, 期 -, 页码 -

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FRONTIERS MEDIA SA
DOI: 10.3389/fmicb.2022.924283

关键词

sugarcane root; physiological function; gene expression; endophytic diazotroph; inoculation

资金

  1. Natural Science Foundation of Guangxi Province [2019GXNSFDA185004, 2021GXNSFAA196041, 2021GXNSFDA196004]
  2. National Natural Science Foundation of China [31701489, 31801288]
  3. Science and Technology Project of Guangxi Province [Guike AD20297130, Guike ZY21195033]
  4. Guangxi Academy of Agricultural Sciences Fund [Guinongke 2021YT09, Guinongke 2021JM01, Guinongke 2021JM68]

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This study found that certain sugarcane germplasms can absorb more nitrogen through bacterial nitrogen fixation. Strain GXS16 can colonize sugarcane roots and exhibit high nitrogenase activity under different environmental conditions. Analysis of plant hormones and gene expression showed that ethylene plays a critical role in regulating the sugarcane root response to GXS16 inoculation.
Some sugarcane germplasms can absorb higher amounts of nitrogen via atmospheric nitrogen fixation through the bacterial diazotrophs. Most endophytic diazotrophs usually penetrate through the root, colonize inside the plant, and fix the nitrogen. To assess the plant's bacterial association during root colonization, strain GXS16 was tagged with a plasmid-bear green fluorescent protein (GFP) gene. The results demonstrated that the strain can colonize roots all the way to the maturation zone. The strain GXS16 showed maximum nitrogenase enzyme activity at pH 8 and 30 degrees C, and nitrogenase activity is less affected by different carbon sources. Further, strain GXS16 colonization response was investigated through plant hormones analysis and RNAseq. The results showed that the bacterial colonization gradually increased with time, and the H2O2 and malondialdehyde (MDA) content significantly increased at 1 day after inoculation. There were no substantial changes noticed in proline content, and the ethylene content was detected initially, but it decreased with time. The abscisic acid (ABA) content showed significant increases of 91.9, 43.9, and 18.7%, but conversely, the gibberellin (GA(3)) content decreased by 12.9, 28.5, and 45.2% at 1, 3, and 5 days after inoculation, respectively. The GXS16 inoculation significantly increased the activities of catalase (CAT), superoxide dismutase (SOD), polyphenol oxidase (PPO), ascorbate peroxidase (APX), and glutathione reductase (GR) at different timepoint. In contrast, the peroxisome (POD) activity had no changes detected during the treatment. In the case of RNAseq analysis, 2437, 6678, and 4568 differentially expressed genes (DEGs) were identified from 1, 3, and 5 days inoculated root samples, and 601 DEGs were shared in all samples. The number or the expression diversity of DEGs related to ethylene was much higher than that of ABA or GA, which indicated the critical role of ethylene in regulating the sugarcane roots response to GXS16 inoculation.

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