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151.
Anne-Catherine Fitchette Marion Cabanes-Macheteau Laure Marvin Barry Martin Batrice Satiat-Jeunemaitre Vronique Gomord Kim Crooks Patrice Lerouge Loïc Faye Chris Hawes 《Plant physiology》1999,121(2):333-344
We recently demonstrated the presence of a new asparagine-linked complex glycan on plant glycoproteins that harbors the Lewis a (Lea), or Galbeta(1-3)[Fucalpha(1-4)]GlcNAc, epitope, which in mammalian cells plays an important role in cell-to-cell recognition. Here we show that the monoclonal antibody JIM 84, which is widely used as a Golgi marker in light and electron microscopy of plant cells, is specific for the Lea antigen. This antigen is present on glycoproteins of a number of flowering and non-flowering plants, but is less apparent in the Cruciferae, the family that includes Arabidopsis. Lea-containing oligosaccharides are found in the Golgi apparatus, and our immunocytochemical experiments suggest that it is synthesized in the trans-most part of the Golgi apparatus. Lea epitopes are abundantly present on extracellular glycoproteins, either soluble or membrane bound, but are never observed on vacuolar glycoproteins. Double-labeling experiments suggest that vacuolar glycoproteins do not bypass the late Golgi compartments where Lea is built, and that the absence of the Lea epitope from vacuolar glycoproteins is probably the result of its degradation by glycosidases en route to or after arrival in the vacuole. 相似文献
152.
153.
Zhi Hong Hua Jin Anne-Catherine Fitchette Yang Xia Andrew M. Monk Lo?c Faye Jianming Li 《The Plant cell》2009,21(12):3792-3802
Asn-linked glycans, or the glycan code, carry crucial information for protein folding, transport, sorting, and degradation. The biochemical pathway for generating such a code is highly conserved in eukaryotic organisms and consists of ordered assembly of a lipid-linked tetradeccasaccharide. Most of our current knowledge on glycan biosynthesis was obtained from studies of yeast asparagine-linked glycosylation (alg) mutants. By contrast, little is known about biosynthesis and biological functions of N-glycans in plants. Here, we show that loss-of-function mutations in the Arabidopsis thaliana homolog of the yeast ALG12 result in transfer of incompletely assembled glycans to polypeptides. This metabolic defect significantly compromises the endoplasmic reticulum–associated degradation of bri1-9 and bri1-5, two defective transmembrane receptors for brassinosteroids. Consequently, overaccumulated bri1-9 or bri1-5 proteins saturate the quality control systems that retain the two mutated receptors in the endoplasmic reticulum and can thus leak out of the folding compartment, resulting in phenotypic suppression of the two bri1 mutants. Our results strongly suggest that the complete assembly of the lipid-linked glycans is essential for successful quality control of defective glycoproteins in Arabidopsis. 相似文献
154.
Six sesquiterpenes were isolated and identified from the essential oil of the wood of Amyris balsamifera (Rutaceae): 10-epi-γ-eudesmol, α-agarofuran, 4-hydroxydihydroagarofuran, valerianol, β-eudesmol, elemol. 相似文献
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156.
Characterization and localization of laccase forms in stem and cell cultures of sycamore 总被引:5,自引:0,他引:5
Azeddine Driouich Anne-Catherine Lainé Brigitte Vian Loic Faye 《The Plant journal : for cell and molecular biology》1992,2(1):13-24
A laccase-type polyphenoloxidase (EC 1.10.3.2.), abundantly secreted by suspension-cultured sycamore (Acer pseudoplatanus) cells was purified to homogeneity. This laccase form is a glycoprotein (molecular weight 110000) with high mannose and complex glycans. The polypeptide moiety has a molecular weight of 66 000, indicating that the glycoprotein is 40% carbohydrate. Laccase is abundantly present in both the cell wall and the culture medium of suspension-cultured sycamore cells, but it is not detected in the cytoplasm, indicating that this large protein is efficiently secreted by the cells. Polyclonal rabbit antiserum was raised against the deglycosylated protein and was used to probe extracts of sycamore stem tissues. A second laccase form (molecular weight 56 000), antigenically related to laccase from cell cultures, is abundant in the epidermis of sycamore stems. In addition, this 56 kDa laccase form co-localizes with lignin precursors on tissue prints from sycamore stems. A polypeptide (molecular weight 50 000-56 000), antigenically related to sycamore laccase, was also immunodetected in most plant organs previously described in the literature as polyphenoloxidase-rich. 相似文献
157.
Azeddine Driouich Pascale Gonnet Mouna Makkie Anne-Catherine Laine Loïc Faye 《Planta》1989,180(1):96-104
Suspension-cultured cells of sycamore (Acer pseudoplatanus L.) secrete a number of acid hydrolases and other proteins that have both highmannose and complex asparagine-linked glycans.
We used affinity chromatography with concanavalin A and an antiserum specific for complex glycans in conjunction with in vivo-labeling
studies to show that all of the secreted proteins carry glycans. The presence of complex glycans on secretory proteins indicates
that they are passing through the Golgi complex on the way to the extracellular compartment. The sodium ionophore, monensin,
did not block the transport of proteins to the extracellular medium, even though monensin efficiently inhibited the Golgi-mediated
processing of complex glycans. The inhibition of N-glycosylation by tunicamycin reduced by 76% to 84% the accumulation of
newly synthesized (i.e. radioactively labeled) protein that was secreted by the sycamore cells, while cytoplasmic protein
biosynthesis was not affected by this antibiotic. However, in the presence of glycoprotein-processing inhibitors, such as
castanospermine and deoxymannojirimycin, the formation of complex glycans was prevented but glycoprotein secretion was unchanged.
These results support the conclusion that N-linked glycan processing is not necessary for sorting, but glycosylation is required
for accumulation of secreted proteins in the extracellular compartment. 相似文献