Metabolic and Transcriptomic Approaches of Chitosan and Water Stress on Polyphenolic and Terpenoid Components and Gene Expression in (Karl.) and .

Farzaneh Khodadadi, Farajollah Shahriai Ahmadi, Majid Talebi, Adam Matkowski, Antoni Szumny, Mahvash Afshari, Mehdi Rahimmalek
Author Information
  1. Farzaneh Khodadadi: Department of Plant Biotechnology, Ferdowsi University of Mashhad, Mashhad 91779-48974, Iran.
  2. Farajollah Shahriai Ahmadi: Department of Plant Biotechnology and Plant Breeding, Ferdowsi University of Mashhad, Mashhad 91779-48974, Iran.
  3. Majid Talebi: Department of Biotechnology, College of Agriculture, Isfahan University of Technology, Isfahan 84156-83111, Iran.
  4. Adam Matkowski: Department of Pharmaceutical Biology and Botany, Wroclaw Medical University, Borowska 211, 50-556 Wroclaw, Poland. ORCID
  5. Antoni Szumny: Department of Food Chemistry and Biocatalysis, Wrocław University of Environmental and Life Sciences, 50-375 Wroclaw, Poland. ORCID
  6. Mahvash Afshari: Department of Agronomy and Plant Breeding, College of Agriculture, Isfahan University of Technology, Isfahan 83111-84156, Iran.
  7. Mehdi Rahimmalek: Department of Food Chemistry and Biocatalysis, Wrocław University of Environmental and Life Sciences, 50-375 Wroclaw, Poland. ORCID

Abstract

In this research, a HPLC analysis, along with transcriptomics tools, was applied to evaluate chitosan and water stress for the prediction of phenolic flavonoids patterns and terpenoid components accumulation in Karel and . The results indicated that the tanshinone contents under drought stress conditions increased 4.2-fold with increasing drought stress intensity in both species. The rosmarinic acid content in the leaves varied from 0.038 to 11.43 mg/g DW. In addition, the flavonoid content was increased (1.8 and 1.4-fold) under mild water deficit conditions with a moderate concentration of chitosan (100 mg L). The application of foliar chitosan at 100 and 200 mg L under well-watered and mild stress conditions led to increases in hydroxyl cryptotanshinone (OH-CT) and cryptotanshinone (CT) contents as the major terpenoid components in both species. The expressions of the studied genes (DXS2, HMGR, KSL, 4CL, and TAT) were also noticeably induced by water deficit and variably modulated by the treatment with chitosan. According to our findings, both the drought stress and the application of foliar chitosan altered the expression levels of certain genes. Specifically, we observed changes in the expression levels of DXS and HMGR, which are upstream genes in the MEP and MVA pathways, respectively. Additionally, the expression level of KSL, a downstream gene involved in diterpenoid synthesis, was also affected. Finally, the present investigation confirmed that chitosan treatments and water stress were affected in both the methylerythritol phosphate pathway (MEP) and mevalonate (MVA) pathways, but their commitment to the production of other isoprenoids has to be considered and discussed.

Keywords

References

  1. Adv Biomed Res. 2023 Mar 21;12:67 [PMID: 37200741]
  2. Antioxidants (Basel). 2020 Jul 29;9(8): [PMID: 32751256]
  3. Cells. 2021 Jan 09;10(1): [PMID: 33435339]
  4. Front Plant Sci. 2023 Jun 02;14:1200898 [PMID: 37332721]
  5. Sci Rep. 2021 Mar 31;11(1):7260 [PMID: 33790349]
  6. Molecules. 2015 Sep 08;20(9):16235-54 [PMID: 26370949]
  7. BMC Genomics. 2014 Jan 28;15:73 [PMID: 24467826]
  8. PLoS One. 2011;6(12):e29713 [PMID: 22242141]
  9. Jundishapur J Nat Pharm Prod. 2014 Oct 04;9(4):e16432 [PMID: 25625046]
  10. BMC Complement Med Ther. 2023 Jun 3;23(1):184 [PMID: 37270541]
  11. PLoS One. 2012;7(11):e46797 [PMID: 23209548]
  12. Biotechnol Appl Biochem. 2007 Apr;46(Pt 4):191-6 [PMID: 17014425]
  13. Plants (Basel). 2021 Jan 28;10(2): [PMID: 33525688]
  14. Sci Rep. 2019 Oct 17;9(1):14929 [PMID: 31624328]
  15. Physiol Mol Biol Plants. 2019 Mar;25(2):313-326 [PMID: 30956416]
  16. Int J Mol Sci. 2020 Jun 23;21(12): [PMID: 32586060]
  17. Plant Physiol Biochem. 2021 Apr;161:166-175 [PMID: 33610861]
  18. Plant Physiol Biochem. 2020 Oct;155:406-415 [PMID: 32814277]
  19. Food Chem. 2022 Dec 15;397:133802 [PMID: 35914462]
  20. BMC Plant Biol. 2018 Oct 26;18(1):258 [PMID: 30367616]
  21. Chem Biodivers. 2018 Mar;15(3):e1700508 [PMID: 29350879]
  22. Plant Physiol Biochem. 2005 Mar;43(3):241-8 [PMID: 15854832]
  23. BMC Plant Biol. 2022 Jul 22;22(1):364 [PMID: 35869431]
  24. Front Pharmacol. 2019 Mar 14;10:202 [PMID: 30923500]

Grants

  1. /Ferdowsi Mashhad University
  2. BPN.ULM.2021.1.00250. U.00001/Polish National Agency for Academic Exchange

MeSH Term

Terpenes
Salvia
Transcriptome
Chitosan
Dehydration
Flavonoids

Chemicals

Terpenes
cryptotanshinone
Chitosan
Flavonoids

Word Cloud

Created with Highcharts 10.0.0chitosanstresswaterdroughtexpressionconditionsgenesHPLCterpenoidcomponentstanshinonecontentsincreasedspeciescontent1milddeficit100mgLapplicationfoliarcryptotanshinoneHMGRKSLalsolevelsMEPMVApathwaysgeneaffectedresearchanalysisalongtranscriptomicstoolsappliedevaluatepredictionphenolicflavonoidspatternsaccumulationKarelresultsindicated42-foldincreasingintensityrosmarinicacidleavesvaried00381143mg/gDWadditionflavonoid84-foldmoderateconcentration200well-wateredledincreaseshydroxylOH-CTCTmajorexpressionsstudiedDXS24CLTATnoticeablyinducedvariablymodulatedtreatmentAccordingfindingsalteredcertainSpecificallyobservedchangesDXSupstreamrespectivelyAdditionallyleveldownstreaminvolvedditerpenoidsynthesisFinallypresentinvestigationconfirmedtreatmentsmethylerythritolphosphatepathwaymevalonatecommitmentproductionisoprenoidsconsidereddiscussedMetabolicTranscriptomicApproachesChitosanWaterStressPolyphenolicTerpenoidComponentsGeneExpressionKarlSalvia

Similar Articles

Cited By