Trienoic Fatty Acids and Plant Tolerance of High Temperature

By Y. Murakami, M. Tsuyama, Y. Kobayashi, H. Kodama, K. Iba. 2000

441 citations recorded by the source corpus.

Subfields: Biochemistry, Molecular Biology, Plant Science

View Paper: https://www.semanticscholar.org/paper/b20b55bcf2d68337c63dc6033603b96f86195886

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In Biochemistry

M. Al-Whaibi

In Molecular Biology

In Plant Science

Citations in the corpus

Brassicaceae germplasm diversity for agronomic and seed quality traits under drought stress (2013, background): “, 2002), tobacco (Kodama et al., 1994; Murakami et al., 2000), and coconut (Repellin et al.”
Growth, lipid peroxidation and photosynthesis in two tall fescue cultivars differing in heat tolerance (2009, background): “PS 2 is the most heat-sensitive component of the photosynthetic system (Murakami et al. 2000, Karim et al. 2003).”
Crop Production under Drought and Heat Stress: Plant Responses and Management Options (2017, background): “A transgenic tobacco plant showing a better photosynthetic activity under heat stress has been produced by alteration of the chloroplast membranes (Murakami et al., 2000).”
Effects of moderate heat stress on photosynthesis: importance of thylakoid reactions, rubisco deactivation, reactive oxygen species, and thermotolerance provided by isoprene (2005, background): “1996) or fatty acid composition of thylakoid membranes (Murakami et al. 2000).”
Physiology and molecular biology of stress tolerance in plants (2006, background): “For example, Murakami et al. (2000) engineered Arabidopisis plants to prevent them from making trienoic fatty acids in their chloroplasts.”
Physiological and Molecular Effects of 24-Epibrassinolide, a Brassinosteroid on Thermotolerance of Tomato (2005, background): “The number of unsaturated lipids (fatty acids with double bond) in thylakoid membrane of chloroplasts- that contain the light absorbing system, electron transport chain and ATP synthase- is important in determining a plant’s ability for growth and photosynthesis at high temperature (Murakami et al. ”
Inhibition of photosynthesis by heat stress: the activation state of Rubisco as a limiting factor in photosynthesis. (2004, background): “However, the relationship between net photosynthesis and electron transport activity is often compromised by the use of extremely high CO2 concentrations for the measurement of leaf photosynthesis in an O2 electrode (Havaux 1993, Murakami et al. 2000, Yamasaki et al. 2002).”
Plant heat-shock proteins: A mini review (2011, positive): “…possibility of using genetic engineering to have more tolerant plants to high temperatures by reducing the degree of saturation of fatty acids in membranes (Murakami et al.,2000) through silencing the enzyme u 3-fatty acid desatur-ase that involves in the synthesis of triple bonds in fatty acids.”
Comprehending crystalline β-carotene accumulation by comparing engineered cell models and the natural carotenoid-rich system of citrus (2011, neutral): “…real-time PCR was performed using the StepOnePlus real-time PCR system (Applied Biosystems, Foster City, CA, USA) and SYBR Premix Ex Taq (Perfect Real Time) reagent (Takara) using gene-speciﬁc primers QAhNRAMP1-F, 5 # -CCTCATCACTGCCTTCGT-3 # and QAhNRAMP1-R, 5 # - ATTGCTGTGTTATCCTTGGTC-3 # .”
Unraveling Field Crops Sensitivity to Heat Stress：Mechanisms, Approaches, and Future Prospects (2018, neutral): “[210] have been developing genetically modified N.”
Rapid Induction of Distinct Stress Responses after the Release of Singlet Oxygen in Arabidopsis Online version contains Web-only data. Article, publication date, and citation information can be found at www.plantcell.org/cgi/doi/10.1105/tpc.014662. (2003, background): “It is the most prominent polyunsaturated fatty acid in chloroplast membrane lipids, accounting for up to 80% of total fatty acids (Murakami et al., 2000).”