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Environmental Responses in Plants

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Cover of 'Environmental Responses in Plants'

Table of Contents

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    Book Overview
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    Chapter 1 Hydrotropism: Analysis of the Root Response to a Moisture Gradient
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    Chapter 2 Assessing Gravitropic Responses in Arabidopsis
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    Chapter 3 Physiological Analysis of Phototropic Responses in Arabidopsis.
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    Chapter 4 Automatic Chloroplast Movement Analysis.
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    Chapter 5 Microscopic and Biochemical Visualization of Auxins in Plant Tissues.
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    Chapter 6 Immunolocalization of PIN and ABCB Transporters in Plants
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    Chapter 7 Analysis of Circadian Leaf Movements
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    Chapter 8 Sample Preparation of Arabidopsis thaliana Shoot Apices for Expression Studies of Photoperiod-Induced Genes.
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    Chapter 9 A Luciferase-Based Assay to Test Whether Gene Expression Responses to Environmental Inputs Are Temporally Restricted by the Circadian Clock.
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    Chapter 10 Identification of Arabidopsis Transcriptional Regulators by Yeast One-Hybrid Screens Using a Transcription Factor ORFeome
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    Chapter 11 Monitoring Alternative Splicing Changes in Arabidopsis Circadian Clock Genes.
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    Chapter 12 Assessing the Impact of Photosynthetic Sugars on the Arabidopsis Circadian Clock.
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    Chapter 13 Assessing Protein Stability Under Different Light and Circadian Conditions.
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    Chapter 14 Screening for Abiotic Stress Tolerance in Rice: Salt, Cold, and Drought.
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    Chapter 15 Basic Techniques to Assess Seed Germination Responses to Abiotic Stress in Arabidopsis thaliana.
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    Chapter 16 Assessing Tolerance to Heavy-Metal Stress in Arabidopsis thaliana Seedlings.
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    Chapter 17 Assessing Drought Responses Using Thermal Infrared Imaging.
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    Chapter 18 Generating Targeted Gene Knockout Lines in Physcomitrella patens to Study Evolution of Stress-Responsive Mechanisms.
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    Chapter 19 Screening Stress Tolerance Traits in Arabidopsis Cell Cultures.
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    Chapter 20 Using Arabidopsis Protoplasts to Study Cellular Responses to Environmental Stress.
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    Chapter 21 Construction of Artificial miRNAs to Prevent Drought Stress in Solanum tuberosum.
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    Chapter 22 Virus-Induced Gene Silencing for Gene Function Studies in Barley.
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    Chapter 23 Methods for Long-Term Stable Storage of Colletotrichum Species.
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    Chapter 24 Plant Inoculation with the Fungal Leaf Pathogen Colletotrichum higginsianum.
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    Chapter 25 Tracing Plant Defense Responses in Roots upon MAMP/DAMP Treatment. - PubMed - NCBI
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    Chapter 26 Analysis of the lmmunity-Related Oxidative Bursts by a Luminol-Based Assay
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    Chapter 27 Quantitative Analysis of Microbe-Associated Molecular Pattern (MAMP)-Induced Ca2+ Transients in Plants
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    Chapter 28 Rapid Assessment of DNA Methylation Changes in Response to Salicylic Acid by Chop-qPCR
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    Chapter 29 Determining Nucleosome Position at Individual Loci After Biotic Stress Using MNase-qPCR
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    Chapter 30 Phosphoprotein Enrichment Combined with Phosphopeptide Enrichment to Identify Putative Phosphoproteins During Defense Response in Arabidopsis thaliana
Attention for Chapter 27: Quantitative Analysis of Microbe-Associated Molecular Pattern (MAMP)-Induced Ca2+ Transients in Plants
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Chapter title
Quantitative Analysis of Microbe-Associated Molecular Pattern (MAMP)-Induced Ca2+ Transients in Plants
Chapter number 27
Book title
Environmental Responses in Plants
Published in
Methods in molecular biology, January 2016
DOI 10.1007/978-1-4939-3356-3_27
Pubmed ID
Book ISBNs
978-1-4939-3354-9, 978-1-4939-3356-3
Authors

Fabian Trempel, Stefanie Ranf, Dierk Scheel, Justin Lee

Editors

Paula Duque

Abstract

Ca(2+) is a secondary messenger involved in early signaling events triggered in response to a plethora of biotic and abiotic stimuli. In plants, environmental cues that induce cytosolic Ca(2+) elevation include touch, reactive oxygen species, cold shock, and salt or osmotic stress. Furthermore, Ca(2+) signaling has been implicated in early stages of plant-microbe interactions of both symbiotic and antagonistic nature. A long-standing hypothesis is that there is information encoded in the Ca(2+) signals (so-called Ca(2+) signatures) to enable plants to differentiate between these stimuli and to trigger the appropriate cellular response. Qualitative and quantitative measurements of Ca(2+) signals are therefore needed to dissect the responses of plants to their environment. Luminescence produced by the Ca(2+) probe aequorin upon Ca(2+) binding is a widely used method for the detection of Ca(2+) transients and other changes in Ca(2+) concentrations in cells or organelles of plant cells. In this chapter, using microbe-associated molecular patterns (MAMPs), such as the bacterial-derived flg22 or elf18 peptides as stimuli, a protocol for the quantitative measurements of Ca(2+) fluxes in apoaequorin-expressing seedlings of Arabidopsis thaliana in 96-well format is described.

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Mendeley readers

The data shown below were compiled from readership statistics for 6 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 6 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 2 33%
Student > Bachelor 1 17%
Professor > Associate Professor 1 17%
Unknown 2 33%
Readers by discipline Count As %
Agricultural and Biological Sciences 3 50%
Biochemistry, Genetics and Molecular Biology 1 17%
Unknown 2 33%