30 research outputs found

    Metabolic response of Platynota stultana pupae during and after extended exposure to elevated CO2 and reduced O2 atmospheres

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    Abstract The metabolic responses of Platynota stultana pupae to reduced O 2 , elevated CO 2 , and their combinations were investigated using microcalorimetry, and mortality of pupae under elevated CO 2 atmospheres was correlated with metabolic responses. The metabolic heat rate decreased slightly with decreasing O 2 concentration until a critical O 2 concentration (P c ) below which the heat rate decreased rapidly. The P c increased with temperature. The percentage decreases of metabolic heat rate were comparable to the percentage decreases of O 2 consumption rate (RO 2 ) at 10, 8, 6, and 4% O 2 , but were smaller at 2 and 1% O 2 . The metabolic heat rate decreased rapidly at 20% CO 2 relative to 0% CO 2 , with little to no further decrease between 20 and 79% CO 2 . The percentage decreases of RO 2 under 20 and 79% CO 2 at 20°C were comparable to the percentage decreases of metabolic heat rates. The additive effects of subatmospheric O 2 and elevated CO 2 levels on reducing metabolic heat rate were generally fully realized at combinations of Յ5% CO 2 and Ն4% O 2 , but became increasingly overlapped as the O 2 concentration decreased and the CO 2 concentration increased. The high susceptibility of pupae to elevated CO 2 at high temperature was correlated with high metabolic heat rate. The metabolic responses of pupae to reduced O 2 concentrations included metabolic arrest and anaerobic metabolism. The net effect of elevated CO 2 on the pupal respiratory metabolism was similar to that of reduced O 2 ; however, mechanisms other than the decrease of metabolism were also contributing to the toxicity of CO 2

    Tomato Fruit Cell Wall Synthesis during Development and Senescence

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    ‘Bartlett’ pear fruit ( Pyrus communis L.) ripening regulation by low temperatures involves genes associated with jasmonic acid, cold response, and transcription factors

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    Low temperature (LT) treatments enhance ethylene production and ripening rate in the European pear (Pyrus communis L.). However, the underlying molecular mechanisms are not well understood. This study aims to identify genes responsible for ripening enhancement by LT. To this end, the transcriptome of ‘Bartlett’ pears treated with LT (0 °C or 10 °C for up to 14 d), which results in faster ripening, and control pears without conditioning treatment was analyzed. LT conditioned pears reached eating firmness (18 N) in 6 d while control pears took about 12 d when left to ripen at 20 °C. We identified 8,536 differentially expressed (DE) genes between the 0 °C-treated and control fruit, and 7,938 DE genes between the 10 °C-treated and control fruit. In an attempt to differentiate temperature-induced vs. ethylene-responsive pathways, we also monitored gene expression in fruit sequentially treated with 1-MCP then exposed to low temperature. This analysis revealed that genes associated with jasmonic acid biosynthesis and signaling, as well as the transcription factors TCP9a, TCP9b, CBF1, CBF4, AGL24, MYB1R1, and HsfB2b could be involved in the LT-mediated enhancement of ripening independently or upstream of ethylene

    ‘Bartlett’ pear fruit ( Pyrus communis L.) ripening regulation by low temperatures involves genes associated with jasmonic acid, cold response, and transcription factors

    No full text
    Low temperature (LT) treatments enhance ethylene production and ripening rate in the European pear (Pyrus communis L.). However, the underlying molecular mechanisms are not well understood. This study aims to identify genes responsible for ripening enhancement by LT. To this end, the transcriptome of ‘Bartlett’ pears treated with LT (0 °C or 10 °C for up to 14 d), which results in faster ripening, and control pears without conditioning treatment was analyzed. LT conditioned pears reached eating firmness (18 N) in 6 d while control pears took about 12 d when left to ripen at 20 °C. We identified 8,536 differentially expressed (DE) genes between the 0 °C-treated and control fruit, and 7,938 DE genes between the 10 °C-treated and control fruit. In an attempt to differentiate temperature-induced vs. ethylene-responsive pathways, we also monitored gene expression in fruit sequentially treated with 1-MCP then exposed to low temperature. This analysis revealed that genes associated with jasmonic acid biosynthesis and signaling, as well as the transcription factors TCP9a, TCP9b, CBF1, CBF4, AGL24, MYB1R1, and HsfB2b could be involved in the LT-mediated enhancement of ripening independently or upstream of ethylene
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