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New insight into the mechanism of cellulose and callose biosynthesis: proteases may regulate callose biosynthesis upon wounding
Authors:Jin Nakashima  Walairat Laosinchai  Xiaojiang Cui  R Malcolm Brown
Institution:(1) Section of Molecular Genetics and Microbiology, School of Biological Sciences, University of Texas at Austin, Austin, TX 78712-1095, USA
Abstract:Using a silver-enhanced, gold-secondary antibody immuno-location approach, we investigated the mechanisms for the switch from beta-1,4- to beta-1,3-glucan biosynthesis upon wounding. Antibodies against beta-1,4- and beta-1,3-glucan synthases were used to locate these synthases before and after wounding of Mung bean (Vigna radiata var Berken) hypocotyls. Within 5 min of wounding, beta-1,4-glucan synthases which were densely localized on plasma membranes adjacent to the secondary walls at the wound site completely disappeared, and beta-1,3-glucan synthases became labeled. The immuno-location of the beta-1,3-glucan synthases in the secondary walls was in good accordance with the region where the beta-1,4-glucan synthases were localized before wounding. Aniline blue was also utilized to visualize the deposition of callose upon wounding. Within 5 min of wounding, callose had accumulated in the corresponding region where the immuno-labeling of beta-1,3-glucan synthase was detected after wounding. The beta-1,3-glucan synthases were always detected from the sieve plate and plasmodesmata which are known to have constitutive synthesis of callose regardless of wounding. Secondary walls located distantly into the tissue away from the wound site were consistently labeled by the beta-1,4-glucan synthase antibody even after wounding. Immuno-blot analysis clearly shows that the levels of beta-1,4-glucan synthase subunit Ces A decreased dramatically within 30 min, whereas the beta-1,3-glucan synthase subunit CFL1 levels increased significantly after wounding. The intensity of labeling reached a maximum at the wound site, and gradually decreased in correspondence with the distance from the wound site. When a protease inhibitor cocktail was applied upon wounding, neither the beta-1,3-glucan synthase appeared nor callose was deposited during the first 5 min of wounding. On the other hand, beta-1,4-glucan synthase was detected at the wound site, implying that activation of beta-1,3-glucan synthase may rely on the degradation of the beta-1,4-glucan synthase. Our study may provide new insight into beta-glucan synthesis in higher plants.
Keywords:beta-1" target="_blank">gif" alt="beta" align="MIDDLE" BORDER="0">-1  3-glucan synthase (callose synthase)  beta-1" target="_blank">gif" alt="beta" align="MIDDLE" BORDER="0">-1  4-glucan synthase (cellulose synthase)  Immuno-light microscopy  Mung bean (Vigna radiata var Berken)  Protease inhibitor cocktail  Secondary wall thickening  Wounding
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