Stipe wall extension of Flammulina velutipes could be induced by an expansin-like protein from Helix aspersa
Autor: | Zhonghua Liu, Wenming Zhang, Hua Wei, Sheng Yuan, Changmei Lu, Hejian Fang, Xin Niu |
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Rok vydání: | 2014 |
Předmět: |
chemistry.chemical_classification
Gastric Juice Snails Turgor pressure Proteins Biology biology.organism_classification Polysaccharide Cell wall chemistry.chemical_compound Expansin Infectious Diseases Stipe (mycology) Chitin chemistry Biochemistry Cell Wall Genetics Biophysics Animals Elongation Ecology Evolution Behavior and Systematics Flammulina |
Zdroj: | Fungal Biology. 118:1-11 |
ISSN: | 1878-6146 |
DOI: | 10.1016/j.funbio.2013.10.003 |
Popis: | Expansin proteins extend plant cell walls by a hydrolysis-free process that disrupts hydrogen bonding between cell wall polysaccharides. However, it is unknown if this mechanism is operative in mushrooms. Herein we report that the native wall extension activity was located exclusively in the 10 mm apical region of 30 mm Flammulina velutipes stipes. The elongation growth was restricted also to the 9 mm apical region of the stipes where the elongation growth of the 1st millimetre was 40-fold greater than that of the 5th millimetre. Therefore, the wall extension activity represents elongation growth of the stipe. The low concentration of expansin-like protein in F. velutipes stipes prevented its isolation. However, we purified an expansin-like protein from snail stomach juice which reconstituted heat-inactivated stipe wall extension without hydrolytic activity. So the previous hypotheses that stipe wall extension was resulted from hydrolysis of wall polymers by enzymes or disruption of hydrogen bonding of wall polymers exclusively by turgor pressure are challenged. We suggest that stipe wall extension may be mediated by endogenous expansin-like proteins that facilitate cell wall polymer slippage by disrupting noncovalent bonding between glucan chains or chitin chains. |
Databáze: | OpenAIRE |
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