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Plant Physiology 60:617-621 (1977)
© 1977 American Society of Plant Biologists

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Articles

{beta}-D-Glucan of Avena Coleoptile Cell Walls 1,2

Donald J. Nevins, Donald J. Huber, Ryoichi Yamamoto and Wayne H. Loescher3

a Department of Botany and Plant Pathology, Iowa State University, Ames, Iowa 50011

A specific glucanase was used to liberate a noncellulosic {beta}-D-glucan from isolated cell walls of Avena sativa coleoptile tissue. Cell walls of this tissue contain as much as 7 to 9 mg of glucan/100 mg of dry wall. Because of the specific action pattern of the enzyme, a linkage sequence of. 1 -> 4 Glc 1 -> 3 Glc 1 -> 4 Glc. is indicated and the predominance of trisaccharide and tetrasaccharide as hydrolytic products suggests a rather regular repeating pattern in the polysaccharide. The trisaccharide and the tetrasaccharide are tentatively identified as 3-O-{beta}-cellobiosyl-D-glucose and 3-O-{beta}-cellotriosyl-D-glucose, respectively. Recovery of these oligosaccharides following glucanase treatment of native wall material was feasible only after wall-bound glucosidases were inactivated. In the absence of enzyme inactivation the released fragments were recovered as glucose. The {beta}-D-glucan was not extracted from walls by either hot water or protease treatment.

Cell walls prepared from auxin-treated Avena coleoptile segments yielded less glucan than did segments incubated in buffer suggesting an auxin effect on the quantity of this wall component. No IAA-induced change in the ratio of the trisaccharide and tetrasaccharide could be detected, suggesting no shift in the 1,3 to 1,4 linkage ratio. While the enzyme acts directly on the {beta}-D-glucan, no elongation response was apparent when Avena sections were treated with the purified glucanase. The presence of the glucan was not associated with any wound response which could be attributed to the preparation of coleoptile segments. The relationship of glucan metabolism to auxin growth responses is discussed.


3 Current address, Department of Horticulture, Washington State University, Pullman.

1 This work was supported by National Science Foundation Research Grant PCM 76-00929.

2 These results were presented in part as a symposium paper entitled "The role of the cell wall in plant growth" at the Midwestern Section meetings of the American Society of Plant Physiologists held at Michigan State University in August 1976.







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Copyright © 1977 by the American Society of Plant Biologists