When French bean (Pbaseolus vulgaris) plants were depodded in the early stages of fruit development, relative levels of a specific protein with a relative molecular weight of 28,000 were enhanced in the young pods that formed later. The protein, designated pod storage protein (PSP), was purified from extracts of newly formed pods from plants that had been previously depodded four times at intervals of 2 weeks. Two-dimensional polyacrylamide gel electrophoresis showed the presence of three forms (designated A, B, and C) of PSP with identical electrophoretic mobilities but different charges. The molecular mass of native PSP was estimated by gel filtration t o be 67 kD; therefore, the protein was most likely present as a dimer. The antisera raised against forms A and C were cross- mobilization in pods during fruit maturation (Tanaka et al., 1993).In the course of studies of endopeptidases in pods of French bean plants, we found that when a large number of pods in the early stages of fruit development were removed from a plant, relative levels of a specific protein with an M, of 28,000 were enhanced in the newly formed pods. The protein accumulated to high levels in the pods of plants that had been previously depodded, whereas a smaller amount was detected in the pods of nontreated plants. It was postulated that enhanced levels of the M, 28,000 protein resulted from a reduction of plant sink size caused by removing pods in the early stages of fruit development.In this report, we characterize this protein from French bean pods and designate it PSP. PSP cDNA clones were isolated, and the deduced amino acid sequence showed 65 to 71% identity with the sequences of VSPs from soybean (Glycine man) leaves (Staswick, 1988) and 40% identity with the sequences of acid phosphatase-1 from tomato (Erion et al., 1991). (Pkaseolus vul-garis) plants, the accumulation of protein in developing pods precedes that in se& (Endo et al., 1987). As reported for other legumes such as field pea (Flinn and Pate, 1968), bean (Oliker, 1978), and cowpea (Peoples et al., 1985a(Peoples et al., , 1985b(Peoples et al., , 1985c, protein accumulates in French bean seeds during fruit development concurrently with active mobilization of protein and free amino acids in the pods. Thus, a proportion of seed nitrogen is temporarily stored in pods Dry seeds of French bean (Phaseolus vulgaris L. cv Goldchased from Sakata Seed (Yokohamat Japan). If stated with 13 h of light (190 p E s-l m-') and 11 h of darkness at 25°C and, at desired developmental stages, maturing fruits were harvested and stored at -20°C until use. For the purification of PSP, pods were collected as follows: just star) and "ybean (Glycine max cv Mikawajima) were purOtherwise, MATERIALS AND METHODS During fruit development in French beanFrench bean plants were grown in a phytotron as proteins, amino acids, and probably small peptides, which are then mobilized to support the growth of seeds.activity throughout the development and subsequent senescence of French bean pods (Endo et al., 1987)....
Pod storage protein (PSP) accumulated in developing pods of French bean (Phaseolus vulgaris L.) plants, and increasing the PSP mRNA level by pod removal resulted in the enhancement of PSP accumulation in pods that formed later. Pod storage protein was detected in flowers, young leaves and young stem internodes in addition to pods. Accumulation of PSP and its mRNA was induced by sink-removal in an organ-specific manner. In addition, wounding induced PSP accumulation systemically in leaves. Methyl jasmonate did not induce PSP synthesis but enhanced the synthesis that was induced by wounding. In senescing pods, PSP was degraded, and degradation products with molecular masses of 20 and 17 kDa were detected in the pods. The amount of 20-kDa degradation product was greater than that of the 17 kDa product.
Metabolism in maize meristem cultures exposed to different heat treatments has been analyzed by 13C-NMR spectroscopy of tissue extracts. The effects of a 40 degrees C permissive stress were compared with a 45 degrees C lethal stress, and the metabolism of glutamate and glutamine were markedly altered by both temperatures. Changes in the incorporation of labeled precursors, alterations due to the in vivo application of enzyme inhibitors, and differences in the activity of enzymes in cell free extracts have confirmed that glutamate synthase (GluS) is partially inactivated by the lethal thermal exposure. This enzyme is quantitatively protected by the induction of thermotolerance. The time dependence for the protection correlates with the appearance of a set of late-arising heat shock proteins (hsps). The function of these late-arising proteins is not yet known, but only one of them, a 67-kDa protein, is spatially correlated with GluS protection. Therefore, the quantitative protection of a key metabolic enzyme has been correlated with the in vivo function of a specific hsp.
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