The effect of glucose concentration and light on thallospore ultrastructure in Ellisomyces anomalus (Thamnidiaceae, Mucorales)

1984 ◽  
Vol 62 (12) ◽  
pp. 2677-2687 ◽  
Author(s):  
Gordon W. Beakes ◽  
Galba M. Campos-Takaki ◽  
Massonori Takaki

The development of chains of thallospores in the mucoraceous fungus Ellisomyces anomalus has been examined using scanning, thin section, and freeze-fracture electron microscopical techniques. The development and cytology of spores formed on high-glucose (HG, 4.0%) and low-glucose (LG, 0.06%) media, under both light and dark conditions, have been compared. The vegetative hyphae of spores on LG media accumulate glycogen particles in their cytoplasm but contain very little lipid. The cytoplasm of HG hyphae is packed with lipid globules. The thallospores are delimited by septa, which as in most other mucoraceous fungi are perforated by plasmodesmatalike pit connections. A thick secondary (spore) wall layer is accreted as the spores swell. Although mature thallospores on LG and HG media are similar in their external morphology, they show internal differences. HG spores are thicker walled and contain abundant lipid and glycogen reserves. LG spores contain relatively little lipid and are more highly vacuolate. The only structural differences observed between the carotene-rich, light-grown spores and their dark-grown counterparts is an increase in lipid globule electron density and an overall enhancement of membrane staining properties. The mature thallospores secede from the parent hyphae by both shizolytic (septum splitting) and rhexolytic (circumcissile hyphal splitting) mechanisms. From a developmental standpoint it is suggested the thallospores of Ellisomyces resemble thallic arthric conidia (arthrospores), simiar to those produced by Mucor rouxii, more closely than true chlamydospores, such as those produced by Gilbertella persicaria and Mucor mucedo.

1987 ◽  
Vol 65 (1) ◽  
pp. 80-94 ◽  
Author(s):  
William Newcomb ◽  
Dwight Baker ◽  
John G. Torrey

An ultrastructural study of effective root nodules of the autumn olive (Elaeagnus umbellata Thunb.) demonstrated the presence of hyphal and vesicular forms of the actinomycete endophyte. No sporangial forms of the endophyte were observed within these nodules. The hyphae contained septa, prominent nucleoid regions, and many ribosomes. The endophytic vesicles were initially nonseptate and then became multichambered as a result of the inward growth of complete and incomplete septa. Glycogen particles were numerous in nonseptate and early stages of septate endophytic vesicle formation and in adjacent hyphae but were absent in more developed stages of septate endophytic vesicles. The endophytic vesicles also contained prominent nucleoid areas, vesicular mesosomes, and crystalline-like striated bodies. A capsule, probably derived from host Golgi cisternae and profiles of dilated rough endoplasmic reticulum, surrounded both forms of the endophyte. The endophytic vesicle cell walls consisted of an outer layer continuous with the hyphal cell wall, a middle clear area or “void space,” and an electron-dense inner layer. The “void space” of the endophyte cell wall was resolved into many thin laminae by freeze–fracture microscopy. The laminae were presumed to be different from the outermost cell wall layer because they were washed out in the solvents used in preparing specimens for the TEM.


1978 ◽  
Vol 56 (7) ◽  
pp. 747-753 ◽  
Author(s):  
P. Jeffries ◽  
T. W. K. Young

Using results obtained with light and scanning electron microscopy of critical-point-dried material and transmission electron microscopy of carbon replicas and freeze-fracture and ultra-thin sections, the structure and germination of the sporangiospore of Phascolomyces articulosus Boedijn is described. The sporangial wall is trilaminate and the ornamented spore wall is two layered. During germination, a new wall layer develops between the plasmalemma and the original spore wall. Sporangial structure is related to that of other members of the Thamnidiaceae and the use of germinating spores of P. articulosus for infection studies of the mycoparasite Piptocephalis unispora is indicated.


Author(s):  
D.J. Benefiel ◽  
R.S. Weinstein

Intramembrane particles (IMP or MAP) are components of most biomembranes. They are visualized by freeze-fracture electron microscopy, and they probably represent replicas of integral membrane proteins. The presence of MAP in biomembranes has been extensively investigated but their detailed ultrastructure has been largely ignored. In this study, we have attempted to lay groundwork for a systematic evaluation of MAP ultrastructure. Using mathematical modeling methods, we have simulated the electron optical appearances of idealized globular proteins as they might be expected to appear in replicas under defined conditions. By comparing these images with the apearances of MAPs in replicas, we have attempted to evaluate dimensional and shape distortions that may be introduced by the freeze-fracture technique and further to deduce the actual shapes of integral membrane proteins from their freezefracture images.


2010 ◽  
Vol 16 (S2) ◽  
pp. 1172-1173
Author(s):  
B Papahadjopoulos-Sternberg ◽  
J Ackrell

Extended abstract of a paper presented at Microscopy and Microanalysis 2010 in Portland, Oregon, USA, August 1 – August 5, 2010.


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