AI Article Synopsis

  • Treatment with plant growth-promoting bacteria (PGPB) producing acdS or transgenic plants with acdS improves salinity tolerance in plants by reducing harmful ethylene levels.
  • The effectiveness of acdS in enhancing salinity tolerance is influenced by the method of delivery, impacting various signaling pathways including ethylene, abscisic acid, auxin, jasmonic acid, and brassinosteroids.
  • Additionally, acdS promotes gene expression related to carbohydrate metabolism, reactive oxygen species management, and even enhances photosynthesis-related genes, despite roots not being photosynthetic tissue.

Article Abstract

treated with plant growth-promoting bacteria (PGPB) producing 1-aminocyclopropane-1-carboxylate deaminase (acdS) or transgenic lines expressing exhibit increased salinity tolerance. AcdS reduces the level of stress ethylene to below the point where it is inhibitory to plant growth. The study determined that several mechanisms appear to be responsible for the increased salinity tolerance and that the effect of acdS on gene expression patterns in roots during salt stress is a function of how it is delivered. Growth in soil treated with the PGPB ( 8R6) mostly affected ethylene- and abscisic acid-dependent signaling in a positive way, while expression of in transgenic lines under the control of the broadly active CaMV promoter or the root-specific promoter affected auxin, jasmonic acid and brassinosteroid signaling and/biosynthesis. The expression of genes involved in minor carbohydrate metabolism were also up-regulated, mainly in roots of lines expressing . Expression of also affected the expression of genes involved in modulating the level of reactive oxygen species (ROS) to prevent cellular damage, while permitting ROS-dependent signal transduction. Though the root is not a photosynthetic tissue, acdS had a positive effect on the expression of genes involved in photosynthesis.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6036250PMC
http://dx.doi.org/10.3389/fmicb.2018.01297DOI Listing

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