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Triticale and barley microspore embryogenesis induction requires both reactive oxygen species generation and efficient system of antioxidative defence

Iwona Żur; Ewa Dubas; Monika Krzewska; Przemysław Kopeć; Anna Nowicka; Ewa Surówka; Katarzyna Gawrońska; Gabriela Gołębiowska; Katarzyna Juzoń; Sabina Malaga
Plant Cell, Tissue and Organ Culture (PCTOC) · Vol. 145, Issue 2 · pp. 347-366 · 2021

Abstract

The effectiveness of microspore embryogenesis (ME) is determined by a complex network of internal and environmental factors. In the present study on triticale and barley, strong positive correlation (r = 0.85) between the generation of hydrogen peroxide (H 2 O 2 ) and ME effectiveness confirmed the important role of reactive oxygen species in microspore reprogramming. However, for high effectiveness of ME induction, intensive H 2 O 2 generation had to be associated with high activity of antioxidative enzymes, superoxide dismutase and catalase. The strong seasonal effect on the physiological status of microspores revealed in the study suggests a kind of ‘biological clock’ controlling plant reproduction, crucial for microspore viability and embryogenic potential. Although the effect of various modifications of ME-inducing stress tiller pre-treatment was determined mainly by the physiological condition of microspores, at higher stress intensity positive effects induced by antioxidant molecules—reduced glutathione and its precursor, l -2-oxothiazolidine-4-carboxylic acid—were observed. High level of variation in the response to ME-inducing stress tiller pre-treatment was also revealed between the two DH lines of triticale and two cultivars of barley and among microspores isolated from subsequently developed spikes.

Bibliographic Information

JournalPlant Cell, Tissue and Organ Culture (PCTOC)
PublisherSpringer
Publication Date2021-05-01
Publication Year2021
Volume145
Issue2
Pages347-366
Document TypeJournal Article
Print ISSN0167-6857
eISSN1573-5044
DOI10.1007/s11240-021-02012-7

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NARA Access Coverage1981-01-01~Current
Journal Homepagehttps://www.springer.com/journal/11240
Publisher PageOpen Publisher Page
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