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Growth, Differentiation and Sexuality

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76 J.P. Latgé <strong>and</strong> R. Calderone<br />

Fig. 5.3. Emergence of polysaccharides in the fungal cell wall<br />

based upon taxonomical clustering <strong>and</strong> fungal evolution fitted<br />

to the geological time scale. Branch lengths are propor-<br />

ancestors, contains both glucan <strong>and</strong> chitin, the<br />

later being present in the highest amount among<br />

all fungi. These two polysaccharides represent<br />

the first in the neosynthesis of a cell wall in the<br />

fungal kingdom, as seen especially in this class<br />

of fungi which exists mostly without a wall. Cell<br />

wall composition evolves from this central core<br />

either positively or negatively. For example, an<br />

evolutionary dead end seen in one branch of the<br />

Zygomycetes, the Mucorales, is the loss of the β1,3<br />

tional to the average nucleotide substitution of nuclear SSU<br />

rDNA sequences (adapted from <strong>and</strong> with J. Taylor; arrow ↓<br />

polysaccharide emerging, arrow ↑ polysaccharide lost)<br />

glucan <strong>and</strong> the occurrence of deacetylated chitin<br />

<strong>and</strong> polymers of uronic acid. Modifications in<br />

other fungal orders consisted mainly of a more or<br />

less complex decoration of this β glucan–chitin<br />

skeleton. Some essential steps in the evolution<br />

are the appearance of α1,3 glucans both in the<br />

Ascomycetes <strong>and</strong> Basidiomycetes. Pentoses are<br />

the hallmark of Basidiomycetes. Galactofuranose<br />

seems to be present only amongst the most<br />

recently evolved fungi, the higher Ascomycetes.

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