Microphotometric determination of structure-bound oxidoreductase activities avoiding nothing-dehydrogenase artefacts: succinate dehydrogenase

 A tetrazolium-based microphotometric method has been devised for the determination of structure-bound dehydrogenase activities with correction for nothing-dehydrogenase artefacts. The method is based on the microphotometric recording of maximum reaction rates in a simple incubation chamber and consists of two successive measurements on the same section, the first in the absence and the second in the presence of the substrate. Following the first measurement, the substrate-free medium is quickly exchanged with the substrate-containing medium and a second measurement is taken. Subtraction of the first from the second reaction rate yields the enzyme activity corrected for nothing-dehydrogenase. Measurements of succinate dehydrogenase (SDH) in skeletal muscle fibres, liver, cardiac atrium and ventricle demonstrate the feasibility of the method. Measurements on the extensor digitorum longus muscle of rat reveal a range of up to fivefold differences in SDH activity within the fibre population of this muscle. Accepted: 11 April 1997     

Dominant resistance to oxythiamin inSaccharomyces cerevisiae and its mapping

A dominant mutation, responsible for the resistance to oxythiamin inSaccharomyces cerevisiae was mapped on the right arm of chromosome IV, 4.6 cM centromere-distally totrp1. The corresponding gene is not involved in the control of intracellular content of total thiamin during growth on a minimal medium without thiamin.     

Changes in nonlinear characteristics of heart rate variability under functional load on the cardiovascular system in healthy subjects and coronary heart disease patients

Some nonlinear characteristics of heart rate variability in the course of functional tests with physical exercise are described. Two groups of volunteers participated in the tests: a control group of 32 healthy subjects (group 1) and a group of 35 coronary heart disease (CHD) patients (group 2). Two series of experiments were performed for each group. An active orthostatic test (AOT) was used in the first series, and a gradually growing physical load on a bicycle ergometer (bicycle ergometer test, BET), in the second series. Along with statistical indices of heart rate (the mean RR interval and standard deviation), nonlinear indices of heart rate were estimated: the correlation dimensionality (D ₂) and approximate entropy (ApEn). Trends of the changes in nonlinear indices of heart rate have been found. The D ₂ and ApEn decreased in both groups of subjects during the AOT and BET under the maximum load. However, the groups of healthy subjects and CHD patients differed in the reactivity of indices, the amplitude of changes in nonlinear indices being narrower in the latter group than in group 1. Differently directed shifts in standard deviation (SDNN) and nonlinear indices have been found. Thus, the data obtained with the use of nonlinear heart rate characteristics show that heart rate under physical load is more multivariate and diverse in healthy subjects at rest and the amplitude of changes during the AOT and BET is greater than in CHD patients, which is a result of the specific autonomic control of heart activity in cardiovascular pathologies.     

Occurrence ofEnterococcus spp. in waters

We studied 630 bacterial strains isolated from surface waters and determined as enterococci on the basis of their growth on Slanetz-Bartley agar in typical colonies. The strains were tested and characterized by several key conventional tests for basic differentiation of enterococci and by commercial test kits. We identified 135 strains ofE. fœcium (21%), 115E. fœcalis (18%), 30E. mundtii (5%), 27E. hirae (4%), 22E. casseliflavus (3%), 21E. gallinarum (3%), 17E. durans-E. hirae complex (3%), 5E. durans (1%), and 1 strain ofE. avium. 150 strains were classified only asEnterococcus sp. (25%) and 107 strains (17%) isolated from Slanetz-Bartley agar were not enterococci. We found that the non-enterococcal group consisted of other Gram-positive cocci and Gram-positive and Gram-negative rods. Based on the identification we tried to find a relation between taxonomic position of isolated strains and their colony morphology on Slanetz-Bartley agar. Out of the total of 523 identified enterococci, 345 strains (66%) formed purple colonies, 136 red colonies (26%), 37 pink colonies (7%) and 5 cream colored colonies (1%). There was no correlation among the color, size or colony morphology and the taxonomic characterization of enterococcal strains.