@article{mbs:/content/journal/micro/10.1099/00221287-143-8-2593, author = "Rosén, Stefan and Sjollema, Klaas and Veenhuis, Marten and Tunlid, Anders", title = "A cytoplasmic lectin produced by the fungus Arthrobotrys oligospora functions as a storage protein during saprophytic and parasitic growth", journal= "Microbiology", year = "1997", volume = "143", number = "8", pages = "2593-2604", doi = "https://doi.org/10.1099/00221287-143-8-2593", url = "https://www.microbiologyresearch.org/content/journal/micro/10.1099/00221287-143-8-2593", publisher = "Microbiology Society", issn = "1465-2080", type = "Journal Article", keywords = "storage protein", keywords = "nematophagous fungus", keywords = "lectin", keywords = "immunolocalization", abstract = "Summary: It was recently shown that the nematode-infecting fungus Arthrobotrys oligospora contains a saline-soluble lectin (designated AOL) that is a member of a novel family of fungal lectins sharing similar primary sequences and binding specificities. During saprophytic growth in liquid cultures, levels of AOL and AOL mRNA were found to vary depending on the growth phase of the mycelium and the carbon/nitrogen (C/N) ratio of the medium. AOL was not detected in young mycelium. In older mycelium (stationary growth phase) grown in media with low C/N ratios (1 or 6), AOL comprised 5-20% of the total amount of saline-soluble proteins present in the mycelium. Neither the lectin nor its transcript was detected in mycelia grown in medium with higher C/N ratios (≥150). Under conditions of nitrogen starvation, AOL was preferentially degraded in relation to the total amount of saline-soluble proteins present in the mycelium. During the infection of nematodes, the level of AOL protein and AOL mRNA increased significantly once the nematodes had been penetrated and digested. Large amounts of AOL accumulated in the trophic hyphae growing inside the nematode as visualized by immunofluorescence microscopy. Later, AOL labelling was detected outside the digested nematodes, preferentially in strands of aggregated hyphae and in newly developed trap cells. Electron microscopy showed that AOL was localized to the cytoplasm and the nucleus of both vegetative mycelium and trap cells, and in the trophic hyphae growing inside the infected nematodes. These results indicate that AOL functions as a storage protein during both saprophytic and parasitic growth.", }