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RAPID ASSEMBLY OF A WOUND PLUG: STAGE ONE OF A TWO‐STAGE WOUND REPAIR MECHANISM IN THE GIANT UNICELLULAR CHLOROPHYTE DASYCLADUS VERMICULARIS (CHLOROPHYCEAE) 1
Author(s) -
Ross Cliff,
Vreeland Valerie,
Herbert Waite J.,
Jacobs Robert S.
Publication year - 2005
Publication title -
journal of phycology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.85
H-Index - 127
eISSN - 1529-8817
pISSN - 0022-3646
DOI - 10.1111/j.1529-8817.2005.04071.x
Subject(s) - biology , biochemistry , spark plug , fructose , galactose , cell wall , botany , microbiology and biotechnology , engineering , aerospace engineering
Upon injury, selected coenocytic algae are capable of forming temporary wound plugs to prevent detrimental cytoplasmic loss. Wound plugs of Dasycladus vermicularis ([Scropoli] Krasser) were harvested 5 min post‐injury and dried. The plug material contained 94% water and can be considered a hydrogel. The gel plug extended several millimeters from the cut end and filled the space inside the cell wall, which resulted from cytoplasmic retraction. Total organic carbon included 55% sugars, 5%–15% protein, and 0.18% lipids. The major sugars were glucose, galactose, mannose, and galacturonic acid. Fluorescein isothiocyanate‐lectins specific for these sugars were localized around the plug matrix. Sulfur content calculated as sulfate corresponded to 17% of the carbohydrate by weight, and sulfated material was detected in plugs by Alcian Blue staining. Formation of the initial plug occurred within 1 min of injury and was not significantly perturbed by the addition of ionic, antioxidant, or chelating agents to the seawater medium. However, addition of exogenous d (+)‐galactose and d (+)‐glucose prevented formation of the nascent gel plug. Wound plugs that were allowed to form from 10 min up until 24 h post‐injury were isolated and incubated with selected biochemical probes to identify the biochemical processes involved in plug formation. The operative strategy in Dasycladus to prevent “cytoplasmic hemorrhage” required availability of sequestered carbohydrate and lectin precursor components throughout the thallus for plug assembly. Once the initial assembly had commenced, additional biochemical interactions were initiated (as a function of time) to promote structural integrity.