scholarly journals Seasonal Changes in the Structure and Function of Mitochondrial Membranes of Artichoke Tubers

1979 ◽  
Vol 64 (5) ◽  
pp. 754-756 ◽  
Author(s):  
Garry N. Hannon ◽  
John K. Raison
1979 ◽  
Vol 63 (2) ◽  
pp. 363-366 ◽  
Author(s):  
Elza Chapman ◽  
Lesley C. Wright ◽  
John K. Raison

Planta ◽  
1975 ◽  
Vol 126 (1) ◽  
pp. 1-10 ◽  
Author(s):  
M. Senser ◽  
F. Sch�tz ◽  
E. Beck

PLoS ONE ◽  
2014 ◽  
Vol 9 (8) ◽  
pp. e105149 ◽  
Author(s):  
Erin Manis ◽  
Todd V. Royer ◽  
Laura T. Johnson ◽  
Laura G. Leff

F1000Research ◽  
2018 ◽  
Vol 7 ◽  
pp. 1983 ◽  
Author(s):  
Mickael M Cohen ◽  
David Tareste

Mitochondria undergo frequent fusion and fission events to adapt their morphology to cellular needs. Homotypic docking and fusion of outer mitochondrial membranes are controlled by Mitofusins, a set of large membrane-anchored GTPase proteins belonging to the dynamin superfamily. Mitofusins include, in addition to their GTPase and transmembrane domains, two heptad repeat domains, HR1 and HR2. All four regions are crucial for Mitofusin function, but their precise contribution to mitochondrial docking and fusion events has remained elusive until very recently. In this commentary, we first give an overview of the established strategies employed by various protein machineries distinct from Mitofusins to mediate membrane fusion. We then present recent structure–function data on Mitofusins that provide important novel insights into their mode of action in mitochondrial fusion.


Author(s):  
R. J. Thompson ◽  
N. A. Ratcliffe ◽  
B. L. Bayne

During recent years attention has been focused on the morphology of the bivalve digestive gland (Sumner, 1966a, b; Owen, 1970; Pal, 1971,1972) but there is little information concerning its role in the storage of energy reserves. Reid (1969) has suggested that in the horse clam, Tresus capax, digestive gland lipid may serve as an energy store which is depleted when food is scarce. Sastry (1966) and Sastry and Blake (1971) have shown that material stored in the digestive tissue of Aequipecten irradians is transferred to the gonad during gametogenesis and Vassallo (1973) has confirmed the transfer of lipid in Chlamys hericia. The digestive gland of My tilus edulis may also have a storage function and may therefore be involved in the utilisation of reserves during starvation. The present paper deals with seasonal changes in the biochemical composition of the digestive gland of M. edulis, and with changes induced by starvation and temperature stress.


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