“…The 138 mu has been found to have glutamate dehydrogenase, malate dehydrogenase, and isocitrate dehydrogenase, all with different Michaelis constants from those present in the host paramecia (41).…”
“…The 138 mu has been found to have glutamate dehydrogenase, malate dehydrogenase, and isocitrate dehydrogenase, all with different Michaelis constants from those present in the host paramecia (41).…”
“…Bacteriophage T4 contains sufficient DNA to code for about 160 proteins. Gibson et al (1971) reported values of 3.3 x lo9 and 3.4 x lo9 daltons for the kinetic complexities of mu endosymbionts of Paramecium aurelia stocks 551 and 540, respectively. Because their paper did not contain details of the conditions of their experiments it is not possible to interpret their results meaningfully.…”
“…The genome complexity of symbiotes in B. culicis was determined in the present study to be 6.7 • 109 daltons. Parallel studies have been made recently in Paramecium endosymbiotes lambda and mu, whose genome complexities are of the order of 108 and l0 P daltons, respectively (15,53). A more recent report on endosymbiotic "xenosomes" of marine ciliates indicates a genome complexity similar to that of lambda (54).…”
Section: Dna Studiesmentioning
confidence: 96%
“…Average values for the genome complexity of DNA's of B. culicis were calculated from rcnaturation rate constants using the procedure and formulae of Wetmur and Davidson(67). Values for genome complexities of other DNA's were obtained from: mu 540 and mu 551(15), lambda 299 (53), E. coli(67), and M. fermentans (PG 18) (2).…”
A new method dependent on immune lysis is described for the isolation of intracellular symbiotes from two species of flagellate protozoa Blastocrithidia culicis and Crithidia oncopeiti. The symbiote-containing flagellates are exposed to complement and antisera prepared in rabbits against symbiote-free organisms. The immune lysis seems to weaken the plasma membranes of the flagellates so that subsequent application of gentle shearing force liberates the intraceUular entities in an undamaged condition. The symbiotes are then separated from other cellular components by DNAse digestion and differential centrifugation. The average recovery of symbiotes isolated by this method is 20%. Light and electron microscopy establishes the structural integrity and numerical abundance of isolated symbiotes in the final fractions. Integrity of symbiotes is further indicated by the high activity of a marker enzyme, uroporphyrinogen I synthetase. The DNA's of symbiote-containing and symbiote-free flagellates, and of isolated symbiotes were purified and compared after isopycnic centrifugation. The comparison establishes the presence of DNA's in symbiotes of both species. The guanine-cytosine (G-C) content of symbiote DNA differs from that of host DNA's in C. oncopelti, but resembles that of kinetoplast DNA in B. culicis. The latter observation was further shown by heat denaturation study. Renaturation kinetics indicate that the genome complexity of symbiote DNA in B. culicis is similar to that of bacteria.
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