Literature DB >> 4165671

Fine structure of quiescent and germinating aeciospores of Cronartium fusiforme.

C H Walkinshaw, J M Hyde, J van Zandt.   

Abstract

Aeciospores of the long-cycle heteroecious rust fungus, Cronartium fusiforme, were found to have an extremely thick cell wall with striking spicules protruding from it. The wall was readily degraded by commercial chitinase, but spicules were unaffected. Quiescent spores contained two nuclei with distinct nuclear membranes possessing many pores. Numerous membrane-bounded lipid bodies were found both in wild-type orange and in white mutant aeciospores. An abundance of irregularly ovoid mitochondria was present in quiescent spores. After glutaraldehydeosmium fixation, the surface of the mitochondria appeared to be covered with ribosomes or microtubules in a paracrystalline array, whereas after permanganate fixation only smooth outer mitochondrial membranes were noted. The latter fixative revealed abundant vesicular endoplasmic reticulum in the spore. Spores incubated at 20 C on agar produced one to five distinct germ tubes within 65 to 180 min. These thin-walled tubes exhibited varying degrees of branching, and reached a total hyphal length of 300 to 500 mu prior to rupturing. Emergence of germ tubes took place through a pore in the spore wall and appeared to be mainly a physical flowing of cytoplasm from the spore into the germ tube without division of nuclei or other cell organelles. On completion of germination, the protoplasm of the germ tube contained both nuclei and nearly all of the other spore contents. Mitochondria had smooth outer membranes, were greatly elongated, and possessed distinct longitudinal cristae. A limited amount of rough endoplasmic reticulum was arranged parallel to the germ tube wall. Other organelles seen in germ tubes were lipid bodies, concentric membrane figures, and numerous ribosomes. Lipid bodies appeared smaller and fewer in number than in quiescent spores.

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Mesh:

Year:  1967        PMID: 4165671      PMCID: PMC251896          DOI: 10.1128/jb.94.1.245-254.1967

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  6 in total

1.  A RELIABLE AND EASILY SECTIONED EPOXY EMBEDDING MEDIUM.

Authors:  W R LOCKWOOD
Journal:  Anat Rec       Date:  1964-10

2.  Ultrastructure of basidiospores and mycelium of Lenzites saepiaria.

Authors:  J M Hyde; C H Walkinshaw
Journal:  J Bacteriol       Date:  1966-10       Impact factor: 3.490

3.  Permanganate; a new fixative for electron microscopy.

Authors:  J H LUFT
Journal:  J Biophys Biochem Cytol       Date:  1956-11-25

4.  AN IMPROVED STAINING METHOD FOR ELECTRON MICROSCOPY.

Authors:  J G STEMPAK; R T WARD
Journal:  J Cell Biol       Date:  1964-09       Impact factor: 10.539

5.  The use of lead citrate at high pH as an electron-opaque stain in electron microscopy.

Authors:  E S REYNOLDS
Journal:  J Cell Biol       Date:  1963-04       Impact factor: 10.539

6.  Cytochemistry and electron microscopy. The preservation of cellular ultrastructure and enzymatic activity by aldehyde fixation.

Authors:  D D SABATINI; K BENSCH; R J BARRNETT
Journal:  J Cell Biol       Date:  1963-04       Impact factor: 10.539

  6 in total
  2 in total

1.  Budding in the dimorphic fungus Phialophora dermatitidis.

Authors:  S N Grove; K B Oujezdsky; P J Szaniszlo
Journal:  J Bacteriol       Date:  1973-07       Impact factor: 3.490

2.  Biochemical changes during fungal sporulation and spore germination. I. Phenyl methyl sulfonyl fluoride inhibition of macroconidial germination in Microsporum gypseum.

Authors:  T J Leighton; J J Stock
Journal:  J Bacteriol       Date:  1970-03       Impact factor: 3.490

  2 in total

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