Titlebook: Biochemical and Cellular Mechanisms of Stress Tolerance in Plants; Joe H. Cherry Conference proceedings 1994 Springer-Verlag Berlin Heidel

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Cross Protection of One Stress by Another: Strategies in Postharvest Fruit Storageein synthesis by inhibiting the synthesis of pre-stress proteins, while heat stress and anaerobic proteins are actively synthesized (Key et al., 1981; Sachs et al., 1980). The alteration of the protein pattern is a reflection of both transcriptional (of stress related proteins) and translational (se

arthroscopy

misanthrope

Altered Gene Expression in Thermoadapted Cultured Cells of Cowpearidization groups and six groups of cDNA clones exhibit increased level of gene expression in thermoadapted cells. We suggest that these non-. genes are involved in the long-term tolerance to hyperthermic stress.

vibrant

Cloning of a Dna Fragment Encoding γ-Glutamyl Kinase and γ-Glutamyl Phosphate Reductase from a Tomatcleotide sequence analysis revealed that the 5’ portion of the . locus contains an 849 bp open reading frame which has the coding capacity for a protein with extensive amino acid sequence similarities to γ-glutamyl kinase from ., yeast and Δ.-pyrroline-5-caroboxylate synthetase from moth bean, and t

誰在削木頭

Regulation of Gene Expression in Response to Drought and Osmotic Shockwith exogenous ABA. However, it was possible to identify some polypeptides specifically induced in osmotically shocked cells, a group of which was also detected in adapted cells. The comparison of protein electrophoretic patterns demonstrated t h a t most changes observed in PEG adapted cells were n

debacle

Gene Expression during Water Stresss available from the same plant for the isolation of molecular components relevant to desiccation. Initially we isolated a large number of cDNA clones which are induced upon dehydration and/or ABA treatment (Bartels et al. 1990, Piatkowski et al. 1990, Bartels et al. 1992).

植物學(xué)

Molecular Genetic Approaches to Improving Heat and Drought Stress Tolerance in Crop Plantscular marker-aided selection. The main reason for this deficiency is the polygenic nature of the stress tolerance traits which makes it difficult to identify a single gene conferring stress tolerance in crop plants. Most of the data collected in stress tolerance research is correlative and cause and

Override

https://doi.org/10.1007/978-94-017-6796-5l., 1990), and by transient activation of heterologous hs promoters, including also the. soybean Gmhspl7.3-B promoter, in tobacco protoplasts (Treuter et al., 1993). The functional analysis of HSF from tomato and Arabidopsis and the manipulation of HSF expression in transgenic plants will have a maj

尊敬

The Ethics and Politics of Subjectivity,e properties of those proteins, in the 15 to 27 kD range. This relates to a rather unique feature of HS in plants in that most plants synthesize a large number of LMW hsps, and some of these are generally the most abundant hsps expressed in plants. Most other eukaryotes, in contrast, synthesize a li

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