Abstract
Pea membranes were incubated with UDP-[14C]xylose or UDP-[14C]arabinose and sequentially extracted with chloroform/methanol/water (10:10:3, by vol.) and sodium dodecyl sulphate (2%, w/v). An active epimerase in the membranes rapidly interconverted the two pentosyl nucleotides. Chromatographic analysis of the lipid extract revealed that both substrates gave rise to xylose- and arabinose-containing neutral lipids, xylolipid with properties similar to a polyisoprenol monophosphoryl derivative, and highly charged lipid-linked arabinosyl oligosaccharide. When UDP-[14C]pentose or the extracted lipid-linked [14C]arabinosyl oligosaccharide were used as substrates, their 14C was also incorporating into sodium dodecyl sulphate-soluble and -insoluble fractions as major end products. Polyacrylamide-gel electrophoresis of sodium dodecyl sulphate-soluble products indicated the formation of mobile components with Mr values between 40 000 and 200 000 (Sepharose CL-6B). The lipid-linked [14C]arabinosyl oligosaccharide possessed properties comparable with those of unsaturated polyisoprenyl pyrophosphoryl derivatives. It was hydrolysed by dilute acid to a charged product (apparent Mr 2300) that could be fractionated in alkali. It was degraded to shorter labelled oligosaccharides by slightly more concentrated acid and eventually to [14C]arabinose as the only labelled component. Susceptibility to acid hydrolysis, and methylation analysis, indicated that the oligosaccharide contained approximately seven sequential alpha-1,5-linked arabinofuranosyl units at the non-reducing end. Several acidic residues appear to be interposed between the terminal arabinosyl units and the charged lipid.
Full text
PDF![791](https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3a5/1153283/e93c4c824de4/biochemj00334-0198.png)
![792](https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3a5/1153283/8b001522af2c/biochemj00334-0199.png)
![793](https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3a5/1153283/fff9a22861b1/biochemj00334-0200.png)
![794](https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3a5/1153283/9f492b8c42c3/biochemj00334-0201.png)
![795](https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3a5/1153283/7049a0413500/biochemj00334-0202.png)
![796](https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3a5/1153283/0a23c81654c1/biochemj00334-0203.png)
![797](https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3a5/1153283/2c4480ac401f/biochemj00334-0204.png)
![798](https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3a5/1153283/91f8bd670e33/biochemj00334-0205.png)
![799](https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3a5/1153283/387fc17c5ae2/biochemj00334-0206.png)
![800](https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3a5/1153283/b0df0da65f98/biochemj00334-0207.png)
![801](https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3a5/1153283/b9c010951ade/biochemj00334-0208.png)
![802](https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3a5/1153283/f50ea9b5efeb/biochemj00334-0209.png)
![803](https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3a5/1153283/c8a68600c8fe/biochemj00334-0210.png)
Images in this article
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Bailey D. S., Deluca V., Dürr M., Verma D. P., Maclachlan G. A. Involvement of Lipid-linked Oligosaccharides in Synthesis of Storage Glycoproteins in Soybean Seeds. Plant Physiol. 1980 Dec;66(6):1113–1118. doi: 10.1104/pp.66.6.1113. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bailey D. S., Dürr M., Burke J., Maclachlan G. The assembly of lipid-linked oligosaccharides in plant and animal membranes. J Supramol Struct. 1979;11(2):123–138. doi: 10.1002/jss.400110203. [DOI] [PubMed] [Google Scholar]
- Bailey R. W., Hassid W. Z. Xylan synthesis from uridine-diphosphate-d-xylose by particulate preparations from immature corncobs. Proc Natl Acad Sci U S A. 1966 Nov;56(5):1586–1593. doi: 10.1073/pnas.56.5.1586. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bolwell G. P., Northcote D. H. Arabinan synthase and xylan synthase activities of Phaseolus vulgaris. Subcellular localization and possible mechanism of action. Biochem J. 1983 Feb 15;210(2):497–507. doi: 10.1042/bj2100497. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Brett C. T., Leloir L. F. Dolichyl monophosphate and its sugar derivatives in plants. Biochem J. 1977 Jan 1;161(1):93–101. doi: 10.1042/bj1610093. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Brett C. T., Northcote D. H. The formation of oligoglucans linked to lipid during synthesis of beta-glucan by characterized membrane fractions isolated from peas. Biochem J. 1975 Apr;148(1):107–117. doi: 10.1042/bj1480107. [DOI] [PMC free article] [PubMed] [Google Scholar]
- CARMINATTI H., PASSERON S., DANKERT M., RECONDO E. SEPARATION OF SUGAR NUCLEOTIDES, PHOSPHORIC ESTERS AND FREE SUGARS BY PAPER CHROMATOGRAPHY WITH SOLVENTS CONTAINING BORATES OF ORGANIC BASES. J Chromatogr. 1965 May;18:342–348. doi: 10.1016/s0021-9673(01)80372-1. [DOI] [PubMed] [Google Scholar]
- Chambers J., Forsee W. T., Elbein A. D. Enzymatic transfer of mannose from mannosyl-phosphoryl-polyprenol to lipid-linked oligosaccharides by pig aorta. J Biol Chem. 1977 Apr 25;252(8):2498–2506. [PubMed] [Google Scholar]
- Delmer D. P., Kulow C., Ericson M. C. Glycoprotein Synthesis in Plants: II. Structure of the Mannolipid Intermediate. Plant Physiol. 1978 Jan;61(1):25–29. doi: 10.1104/pp.61.1.25. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dürr M., Bailey D. S., MacLachlan G. Subcellular distribution of membrane-bound glycosyltransferases from pea stems. Eur J Biochem. 1979 Jul;97(2):445–453. doi: 10.1111/j.1432-1033.1979.tb13132.x. [DOI] [PubMed] [Google Scholar]
- Ericson M. C., Chrispeels M. J. Isolation and Characterization of Glucosamine-containing Storage Glycoproteins from the Cotyledons of Phaseolus aureus. Plant Physiol. 1973 Aug;52(2):98–104. doi: 10.1104/pp.52.2.98. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ericson M. C., Delmer D. P. Glycoprotein synthesis in plants: I. Role of lipid intermediates. Plant Physiol. 1977 Mar;59(3):341–347. doi: 10.1104/pp.59.3.341. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ericson M. C., Gafford J. T., Elbein A. D. Tunicamycin inhibits GlcNAc-lipid formation in plants. J Biol Chem. 1977 Nov 10;252(21):7431–7433. [PubMed] [Google Scholar]
- FEINGOLD D. S., NEUFELD E. F., HASSID W. Z. The 4-epimerization and decarboxylation of uridine diphosphate D-glucuronic acid by extracts from Phaseolus aureus seedlings. J Biol Chem. 1960 Apr;235:910–913. [PubMed] [Google Scholar]
- Faltynek C. R., Silbert J. E., Hof L. Xylosylphosphoryldolichol synthesized by chick embryo epiphyses. Not an intermediate in proteoglycan biosynthesis. J Biol Chem. 1982 May 25;257(10):5490–5495. [PubMed] [Google Scholar]
- Floyd R. W., Stone M. P., Joklik W. K. Separation of single-stranded ribonucleic acids by acrylamide-agarose-urea gel electrophoresis. Anal Biochem. 1974 Jun;59(2):599–609. doi: 10.1016/0003-2697(74)90313-3. [DOI] [PubMed] [Google Scholar]
- Forsee W. T., Elbein A. D. Biosynthesis of mannosyl- and glucosyl-phosphoryl-polyprenols in cotton fibers. J Biol Chem. 1973 Apr 25;248(8):2858–2867. [PubMed] [Google Scholar]
- Forsee W. T., Elbein A. D. Glycoprotein biosynthesis in plants. Demonstration of lipid-linked oligosaccharides of mannose and N-acetylglucosamine. J Biol Chem. 1975 Dec 25;250(24):9283–9293. [PubMed] [Google Scholar]
- García R. C., Recondo E., Dankert M. Polysaccharide biosynthesis in Acetobacter xylinum. Enzymatic synthesis of lipid diphosphate and monophospate sugars. Eur J Biochem. 1974 Mar 15;43(1):93–105. doi: 10.1111/j.1432-1033.1974.tb03389.x. [DOI] [PubMed] [Google Scholar]
- Gleeson P. A., Clarke A. E. Antigenic determinants of a plant proteoglycan, the Gladiolus style arabinogalactan-protein. Biochem J. 1980 Nov 1;191(2):437–447. doi: 10.1042/bj1910437. [DOI] [PMC free article] [PubMed] [Google Scholar]
- HAKOMORI S. A RAPID PERMETHYLATION OF GLYCOLIPID, AND POLYSACCHARIDE CATALYZED BY METHYLSULFINYL CARBANION IN DIMETHYL SULFOXIDE. J Biochem. 1964 Feb;55:205–208. [PubMed] [Google Scholar]
- Hayashi T., Matsuda K. Biosynthesis of xyloglucan in suspension-cultured soybean cells. Occurrence and some properties of xyloglucan 4-beta-D-glucosyltransferase and 6-alpha-D-xylosyltransferase. J Biol Chem. 1981 Nov 10;256(21):11117–11122. [PubMed] [Google Scholar]
- Herscovics A., Warren C. D., Jeanloz R. W., Wedgwood J. F., Liu I. Y., Strominger J. L. Occurrence of a beta-D-mannopyranosyl phosphate residue in the polyprenyl mannosyl phosphate formed in calf pancreas microsomes and in human lymphocytes. FEBS Lett. 1974 Sep 1;45(1):312–317. doi: 10.1016/0014-5793(74)80869-0. [DOI] [PubMed] [Google Scholar]
- Hopp H. E., Romero P. A., Daleo G. R., Pont Lezica R. Synthesis of cellulose precursors. The involvement of lipid-linked sugars. Eur J Biochem. 1978 Mar 15;84(2):561–571. doi: 10.1111/j.1432-1033.1978.tb12199.x. [DOI] [PubMed] [Google Scholar]
- Karr A. L. Isolation of an enzyme system which will catalyze the glycosylation of extensin. Plant Physiol. 1972 Aug;50(2):275–282. doi: 10.1104/pp.50.2.275. [DOI] [PMC free article] [PubMed] [Google Scholar]
- LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
- Laemmli U. K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970 Aug 15;227(5259):680–685. doi: 10.1038/227680a0. [DOI] [PubMed] [Google Scholar]
- Lehle L., Fartaczek F., Tanner W., Kauss H. Formation of polyprenol-linked mono- and oligosaccharides in Phaseolus aureus. Arch Biochem Biophys. 1976 Aug;175(2):419–426. doi: 10.1016/0003-9861(76)90529-4. [DOI] [PubMed] [Google Scholar]
- Lezica R. P., Brett C. T., Martinez P. R., Dankert M. A. A glucose acceptor in plants with the properties of an alpha-saturated polyprenyl-monophosphate. Biochem Biophys Res Commun. 1975 Oct 6;66(3):980–987. doi: 10.1016/0006-291x(75)90736-6. [DOI] [PubMed] [Google Scholar]
- Lis H., Sharon N. Soybean agglutinin--a plant glycoprotein. Structure of the carboxydrate unit. J Biol Chem. 1978 May 25;253(10):3468–3476. [PubMed] [Google Scholar]
- ROBYT J., FRENCH D. Action pattern and specificity of an amylase from Bacillus subtilis. Arch Biochem Biophys. 1963 Mar;100:451–467. doi: 10.1016/0003-9861(63)90112-7. [DOI] [PubMed] [Google Scholar]
- Rees D. A., Richardson N. G. Polysaccharides in germination. Occurrence, fine structure, and possible biological role of the pectic araban in white mustard cotyledons. Biochemistry. 1966 Oct;5(10):3099–3107. doi: 10.1021/bi00874a003. [DOI] [PubMed] [Google Scholar]
- Sandford P. A., Conrad H. E. The structure of the Aerobacter aerogenes A3(S1) polysaccharide. I. A reexamination using improved procedures for methylation analysis. Biochemistry. 1966 May;5(5):1508–1517. doi: 10.1021/bi00869a009. [DOI] [PubMed] [Google Scholar]
- Staneloni R. J., Tolmasky M. E., Petriella C., Ugalde R. A., Leloir L. F. Presence in a plant of a compound similar to the dolichyl diphosphate oligosaccharide of animal tissue. Biochem J. 1980 Oct 1;191(1):257–260. doi: 10.1042/bj1910257. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Talmadge K. W., Keegstra K., Bauer W. D., Albersheim P. The Structure of Plant Cell Walls: I. The Macromolecular Components of the Walls of Suspension-cultured Sycamore Cells with a Detailed Analysis of the Pectic Polysaccharides. Plant Physiol. 1973 Jan;51(1):158–173. doi: 10.1104/pp.51.1.158. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Waechter C. J., Lennarz W. J. The role of polyprenol-linked sugars in glycoprotein synthesis. Annu Rev Biochem. 1976;45:95–112. doi: 10.1146/annurev.bi.45.070176.000523. [DOI] [PubMed] [Google Scholar]
- Waechter C. J., Lucas J. J., Lennarz W. J. Evidence for xylosyl lipids as intermediates in xylosyl transfers in hen oviduct membranes. Biochem Biophys Res Commun. 1974 Jan 23;56(2):343–350. doi: 10.1016/0006-291x(74)90848-1. [DOI] [PubMed] [Google Scholar]
- Yamagishi T., Matsuda K., Watanabe Y. Characterization of the fragments obtained by enzymic and alkaline degradation of rice-bran proteoglycans. Carbohydr Res. 1976 Aug;50(1):63–74. doi: 10.1016/s0008-6215(00)84083-5. [DOI] [PubMed] [Google Scholar]