Detection and characterization of methyl parathion-resistant Chlorella protothecoides.
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Biomedical subjects
Publications and source records attributed to S Bose.
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A 52-yr-old man had chronic recurrent pseudo-obstruction of the colon, along with multisystem disease secondary to progressive systemic sclerosis (PSS). D-Penicillamine treatment reversed the PSS, which involved the duodenum, small and large intestines, lungs, myocardium, and proximal and peripheral skin. The improvement was documented by electrocardiogram pulmonary function studies, roentgenography of gastrointestinal tract, and by repeated skin biopsies. Hand blood-volume studies using 99m Tc also revealed improvement of PSS in both hands. A variable degree of improvement was documented in seven additional patients with PSS. Follow-up periods were 18 mo to 4 yr. The most common side effect of the drug was transient hypogeusia, and no patient showed a serious side effect. This article includes a review of the literature on penicillamine therapy for PSS.
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The light saturated rate of photosystem I-dependent electron transport (ascorbate/dichlorophenol-indophenol --> methyl vilogen in presence of 1 micromolar 3-[3,4-dichlorophenyl]-1,1-dimethyl urea [DCMU]) was increased by a high concentration of DCMU added to broken and uncoupled chloroplasts isolated from pea (Pisum sativum). At 50 micromolar DCMU, the increase was around 50%. No stimulation was observed under limiting intensity of illumination, indicating that the relative quantum yield of electron transport was not affected by high DCMU. The light-saturated rate in coupled (to proton gradient formation) chloroplasts was unchanged by 50 micromolar DCMU, suggesting that the rate-limitation imposed by energy coupling was not affected. Using N,N,N',N'-tetramethyl-p-phenylene diamine as electron donor, essentially no DCMU stimulation of the rate was observed, indicating further that the electron donation at a site close to P700 was not affected by high DCMU. It is concluded that DCMU, in the range of 10 to 50 micromolar, affected the thylakoid membranes in such a way that the rate constant of electron donation by dichlorophenol-indophenol at the site prior to the site of energy coupling increased. Further observations that DCMU at 100 micromolar stimulated the rate in coupled chloroplasts indicated an additional DCMU action, presumably by uncoupling the chloroplasts from phosphorylation, as suggested by Izawa (Shibata et al., eds, Comprehensive Biochemistry and Biophysics of Photosynthesis, University Press, State College, Pennsylvania, pp 140-147, 1968). A scheme has been proposed for multiple sites of DCMU action on the electron transport system in chloroplasts.
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The role of the vitamin C was explored in the uropygial gland of the juvenile pigeons from histological and karyodynamic standpoints. Furthermore, the total lipid of the gland was also measured. Vitamin C loading increased the gland weight without causing any perceptible change in the mitotic activity of the gland or in the glandular lipid level in either sex of the juvenile pigeons. Significance of these findings has been briefly discussed.
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Cation regulation of excitation energy distribution was examined in chloroplasts isolated from (a) pea seedlings, grown in intermittent illumination, which contain no light-harvesting complex, (b) a barley mutant which is deficient in the major polypeptide component of the light-harvesting complex, and (c) a soybean mutant which contains a reduced amount of light-harvesting complex. It was found that: (1) Mg2+-induced increase in Photosystem II fluorescence at room temperature is small in the chloroplasts of the soybean mutant, smaller in the barley mutant, and almost absent in the light-harvesting complex-less chloroplasts of pea as compared to their respective controls. (2) Mg2+-induced increase in the F685/F730 emission peak ratio at 77 K is not detected in the isolated chloroplasts of the intermittent light-grown pea and the barley mutant. (3) Pre-illumination induced State 1-State 2 and adaptation in vivo is absent in the barley mutant and is less pronounced in the soybean mutant as compared to their respective controls. (4) Increase of slow fluorescence decay upon addition of Mg2+ observed in control chloroplasts was not detected in chloroplasts of intermittent-light grown peas. These results confirm earlier conclusions (Armond, P.A., Arntzen, C.J., Briantais, J.M. and Vernotte, C. (1976) Arch. Biochem. Biophys. 175, 54--63; Davis, D.J., Armond, P.A., Gross, E.L. and Arntzen, C.J. (1976) Arch. Biochem. Biophys. 175, 64--70) that light-harvesting complex is required for the Mg2+-induced regulation of the excitation energy distribution between Photosystems I and II. The characteristic P-S decay and I-D dip of the in vivo fluorescence inductions (Kautsky effect) were not significantly altered in the light-harvesting complex-less and the light-harvesting complex-deficient chloroplasts as compared to their respective controls. These results indicate that light-harvesting complex is not obligatorily required to observe the P-S decay or the I-D dip.
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The rare association of protease inhibitor deficiency (Pi(zz) genotype) in a black American with chronic, obstructive pulmonary disease due to asthmatic bronchitis, rather than basal pan lobular emphysema, is presented. The late onset of symptoms, despite environmental exposures, is also unusual in this homozygote, as is his ethnic background.
An epidemiologic study of protease inhibitor (alpha(1)-antitrypsin) was undertaken among 599 ambulatory and hospitalized black American patients with chronic cardiopulmonary disease referred for pulmonary function testing, and 115 ethnically matched, healthy control subjects. Clinical evaluation consisted of respiratory questionnaire completion, physical examination, chest radiograph, and spirography. Protease inhibitor evaluation consisted of measurement of serum trypsin inhibitory capacity in all subjects corrected by comparison with control sera, while 200 of these subjects were phenotyped for alpha(1)-antitrypsin electrophoretic variants.Results showed mean serum trypsin inhibitory capacity for all subjects was 1.56, SD ± 0.47 mg/ml, while corrected values were 111.2, SD ± 30.5 percent of control. Acute phase reactivity was present for patients with heart disease, pulmonary malignancy, p<0.01 for both, and pulmonary fibrosis, p<0.05, when compared with controls. Prevalence of protease inhibitor variants in 29 controls was two heterozygotes for the Z variant (seven percent), and one homozygote for the S variant. Among 94 patients with chronic obstructive pulmonary disease, prevalence was 1.1 percent each for ZZ and SZ phenotypes, and 2.1 percent for MZ. Suprprisingly, the sole ZZ patient had asthmatic bronchitis rather than emphysema.Computed allele frequencies for Pi M and Z were comparable to those for a random sample of black Americans in St. Louis, but differed from a sample of black infants in Brooklyn, NY.These results indicate that protease inhibitor deficiency variants are not as uncommon among black Americans as the literature suggests. Furthermore, the heterozygous state is not necessarily a risk factor in development of chronic obstructive pulmonary disease. Protease inhibitor deficiency states therefore appear to play less important a role in etiology of chronic cardiopulmonary disease in black Americans than among their Caucasian counterparts.Preliminary work was published in abstract form.(1)
The role of the carbohydrate moiety in influencing the survival time of human lymphoblastoid interferon in the rat circulation was monitored at varying time intervals after intravenous injection. The serum survival time of native interferon was drastically reduced by prior enzymatic cleavage of the terminal sialic acid residues to yield the galactose-terminal product, asialo-interferon. This phenomenon was completely reversed by further extensive digestion with a mixture of glycosidases which effectively removed over 85% of the total carbohydrate residues. These results suggest that the intact carbohydrate structure is neither essential for normal circulation time in vivo nor for biologic activity in vitro.