By D. A. Day, R. Douce (auth.), Dr. Roland Douce, Dr. David A. Day (eds.)
I am commemorated via the editor's invitation to put in writing a Preface for this quantity. As a member of an older new release of plant physiologists, my lineage in plant respiratory strains again to F. F. BLACKMAN in the course of the privilege of getting M. THOMAS and W. O. JAMES, of his "students," as my mentors. How the topic has replaced in forty years! In these darkish a while B. 14C. many of the info on hand used to be hard-won from long term experiments utilizing the input-output procedure. breathing adjustments according to remedies have been measured through hard gasoline research or by way of titration of alkali from lots of Pettenkofer tubes; the Warburg respir ometer was once simply commencing to be used for plant reports by way of pioneers comparable to TURNER and ROBERTSON. however the classical experiments of BLACKMAN with apples had ended in very important effects at the kinfolk among anaerobic and cardio carbohydrate usage and at the climacteric, and to the 1st specific inspiration of breathing regulate of breathing imposed through the" organiza tion resistance" of mobilephone constitution. THOMAS prolonged this procedure in his investi gations of the Pasteur impact and the induction of cardio fermentation via poi sons reminiscent of cyanide and excessive concentrations of CO , JAMES started an extended 2 sequence of reviews of the partial reactions of respiratory in extracts from barley and YEMM'S precise research of carbohydrate parts when it comes to respira tory adjustments further a huge new dimension.
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Additional info for Higher Plant Cell Respiration
Fig. 3). This structure appears to be a good compromise since it reconciles the major discrepancies mentioned above, namely - the heterogeneity in size distribution of the mtDNA molecules observed by electron microscopy - the complex restriction patterns which contain nonstoichiometric bands (related to the stoichiometry of the different circles) and very faint bands Gunction fragments related to the recombinations). Whether all the native mtDNA molecules are circular or not remains still unsolved.
In contrast, other workers have shown that the presence of even trace amounts of galactosyglycerides is due to contamination from plastids (BEN ABDELKADER 1972, MCCARTY etal. L. and DOUCE R. 1982, unpublished results). Methods have been developed in several laboratories by which inner and outer mitochondrial membranes can be separated from each other. These include the use of osmotic shock, Yeda press treatment, or detergent treatment of isolated mitochondria. In an early study of potato tuber mitochondrial membranes (MEUNffiR and MAZLIAK 1972), there were indications of an enrichment of diphosphatidylglycerol and other acidic phospholipids in the inner membrane, while the outer membrane contained high amounts of phosphatidy1choline.
Lm in maize; SYNENKI et al. lm. lm in wheat; no discrete classes were apparent. lm without discrete classes. lm to KOLODNER and TEWARI (1972) but recent observation (SEVIGNAC and QUETmR, unpublished) showed well-dispersed sizes. lm, but more recently isolated different circular mtDNA species (BRENNICKE and BLANZ 1982). The general situation now is that the size distribution of circular molecules is heterogeneous regardless of whether discrete classes can be discerned. lm have been observed and some of these may be related to cytoplasmic male sterility (maize, KEMBLE and BEDBROOK 1980, WEISSINGER et al.