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41.
The dependence of growth on nickel supply was studied in Chlorella emersonii 211-8b. After transfer to Ni2+ deficient medium containing only 0.5±0.2 g/l of Ni2+, production of biomass or daughter cells dropped to 55±5% of the controls, and the cells became chlorotic. These symptoms of deficiency disappeared completely by supplying adequate amounts of nickel. They were, however, only partially reversible by cobalt. It is concluded that nickel is an essential micronutrient for C. emersonii, although this organism lacks the nickel enzyme, urease.Gratefully dedicated to Prof. Hans Adolf von Stosch on the occasion of his 70th birthday 相似文献
42.
Christiane Lichtlé 《Protoplasma》1980,102(1-2):11-19
Summary C.rufescens excystment, experimentally induced, corresponds to a general metabolism recovery of the cell, previously in a resting phase. The cytoplasm changes without any polarity, and organelles like gullet and flagella redifferentiate. The thylakoids develop mainly from the stored lipidic compounds which then disappear. Phycoerythrin immediately fills the intrathylakoidal lumen. Pigment synthesis seems closely associated with the development of membranes. The activated cell divides and the cyst wall breaks down. The destruction of the wall begins in the median layer and is followed by a mechanical rupture of the external and internal layers. Each germinative cyst releases two or four fully differentiated cells. There is an exact symmetry between excystment and encystment, all the transformations of theC. rufescens cell being reversible. 相似文献
43.
Ingrid Lombeck K. Kasperek L. E. Feinendegen H. J. Bremer 《Biological trace element research》1980,2(3):193-198
The rubidium content of whole blood was estimated by instrumental neutron activation analysis. In 46 healthy children it amounts
to {ie193-1} g/g dry weight. There was no difference between the values found for infants, toddlers, and school children.
In 29 dietetically treated patients with phenylketonuria and maple-syrup-urine disease the values were significantly lower
than in healthy children. During the first three months of diet therapy the rubidium levels remained in the lower range of
the normal values, decreasing to about 60% of the mean of normal values later on. With increasing length of diet therapy these
values tended to decrease. It remains questionable whether these decreased levels reflect only an induced biochemical phenomenon
without biological importance, or whether they are the first signs of a deficiency syndrome. 相似文献
44.
Edith Wallace Harold I. Calvin George W. Cooper 《Molecular reproduction and development》1983,7(4):377-387
Three successive generations of mice were fed a Torula yeast based Se-deficient diet with or without 0.1 ppm Se in the drinking water. The Se-deficient mice, in the course of three generations, showed a decrease in body weight, testis weight, epididymal weight, and sperm production. The percentage of morphologically abnormal sperm increased in successive generations. The majority of sperm defects were found in the midpiece region of the tail. Many of these aberrant sperm were motile. A progressive decrease in fertility was noted during the first two generations of Se deficiency. This system confirms the essential role of Se in spermatogenesis and provides a model for the evaluation of the primary effect of Se deprivation on the structural development of sperm. 相似文献
45.
Liver tissues and fibroblasts from patients with propionic acidemia assigned to the pcc BC genetic complementation group have previously been shown to contain normal or near-normal quantities of structurally altered propionyl CoA carboxylases (PCC). Biochemical comparisons of PCCs from extracts of three livers and one placenta belonging to the pcc BC complementation group revealed that the K
m values for the enzyme's major substrates, propionyl CoA, bicarbonate, and ATP, and its monovalent activator, potassium, were similar to those of normal PCC. PCC in extracts of one of the livers, however, had an altered isoelectric point (pI = 5.4) compared to that of PCC from normal and other PCC-deficient tissues (pK = 4.6–4.7). Thermostability in the presence of sucrose or ATP differed among several of the mutant PCCs, including the PCC with an altered pI, and from that of normal PCC. To confirm these results and to determine whether valid inferences may be derived from comparisons of mutant and normal PCC in crude extracts, PCC was purified from normal liver and from one of the PCC-deficient livers. The biochemical parameters of the purified carboxylases were similar to those observed in liver extracts. These studies further-more confirmed that, whether purified or in extracts, PCC from the pcc BC group reflects structural mutations. Nevertheless, the abnormal enzyme structure appears to have no corresponding effect on the clinical features of the disorder in various affected individuals. Moreover, there is biochemical heterogeneity within the pcc BC complementation group that probably represents different interallelic gene mutations.This work was supported by NIH Research Grants Am 25675 and AM 26127. B. Wolf is the recipient of NIH Research Career Development Award AM 00677 and is aided by Basil O'Connor Starter Research Grant 5-263 from The National Foundation-March of Dimes. This article is No. 131 from the Department of Human Genetics at the Medical College of Virginia. 相似文献
46.
I. G. Burns 《Plant and Soil》1992,142(2):221-233
A method is described for determining the way in which growth rate varies with plant nutrient concentration using a simple
nutrient interruption technique incorporating only 2 treatments. The method involves measuring the changes in growth and nutrient
composition of otherwise well-nourished plants after the supply of one particular nutrient has been withheld. Critical concentrations
are estimated from the relationship between the growth rate (expressed as a fraction of that for control plants of the same
size which remained well-nourished throughout) and the concentration of the growth-limiting nutrient in the plants as deficiency
developed. Trials of the method using young lettuce plants showed that shoot growth rate was directly proportional to total
N (nitrate plus organic N) concentration, and linearly or near-linearly related to K and P concentration over a wide range;
the corresponding relationship for nitrate was strongly curvi-linear. Critical concentrations (corresponding to a 10% reduction
in growth rate) determined from these results were similar to critical values calculated from models derived from field data,
but were generally higher than published estimates of critical concentration (based on reductions in shoot weight) for plants
of a similar size. Reasons for these discrepancies are discussed. Nitrate, phosphate or potassium concentrations in sap from
individual leaf petioles were highly sensitive to changes in shoot growth rate as deficiency developed, with the slope of
the relationships varying with leaf position, due to differences both in their initial concentration and in the rates at which
they were utilized in individual leaves. Each nutrient was always depleted more quickly in younger leaves than in older ones,
providing earlier evidence of deficiency for diagnostic purposes. Although the plants were capable of accumulating nitrate,
phosphate and potassium well in excess of that needed for optimum dry matter production during periods of adequate supply,
the rate of mobilization of these reserves was insufficient to prevent reductions in growth rate as the plants became deficient.
This brings into question the validity of the conventional concept that luxury consumption provides a store of nutrients which
are freely available for use in times of shortage. The implications of these results for the use of plant analysis for assessing
plant nutrient status are discussed. 相似文献
47.
The etiology of selenium-vitamin E (Se-E) deficiency diseases may be complex. Many of the syndromes involve combined deficiency
of selenium and vitamin E. Selenium moves into the animal and human food chain from soil and plants, which may contain inadequate
amounts of the nutrient in many areas of the world. Vitamin E may be in low concentration in many animal feeds unless supplements
are added. Some syndromes, such as steatitis in cats, result from an increased requirement of vitamin E in diets that contain
large amounts of polyunsaturated fatty acids, and these diseases will only respond to vitamin E administration. Deficiency
syndromes in animals owing to pure Se deficiency are infrequent and have been produced mainly by laboratory studies utilizing
extreme deficiency conditions. Other factors that may affect the occurrence of these deficiency diseases are concurrent dietary
deficiency of S-containing amino acids, bioavailability of different forms of dietary Se, intake of compounds that antagonize
Se (e.g., silver salts), and exposure to various prooxidant substances (e.g., iron compounds, oxygen, ozone, and various drugs).
A wide variety of pathologic alterations occur in animals and humans with Se-E deficiency. Myocardial lesions are seen most
frequently in calves, lambs, pigs, turkey poults, and ducklings. In humans, Keshan disease, an endemic cardiomyopathy in China,
is attributed to Se deficiency. Necrosis of skeletal muscle is the most frequent lesion observed in animal species. Necrosis
of smooth muscle of the gizzard and intestine may be a prominent lesion in turkey poults, ducklings, and quail. Other Se-E
deficiency lesions include hepatic necrosis, gastric ulceration, intestinal and uterine lipofuscinosis, pancreatic damage,
steatitis, exudative diathesis, encephalomalacia, and testicular necrosis. Selenium toxicosis is well characterized in animals
and humans by neurological, hoof, and hair alterations. 相似文献
48.
Erkki Hltt Pirkko Pohjanpelto 《Biochimica et Biophysica Acta (BBA)/Molecular Cell Research》1982,721(4):321-327
We recently isolated a Chinese hamster ovary cell line which grows well without serum but requires the exogenous polyamines putrescine, spermidine or spermine for continuous replication. Here we show that these cells are defective in the arginase-catalyzed synthesis of ornithine, the precursor of polyamines, and that ornithine can replace polyamines in the medium for supporting growth of the cells. The activities of two other key enzymes of polyamine biosynthesis, ornithine decarboxylase and adenosylmethionine decarboxylase, are clearly detectable and show increase during polyamine starvation. In ornithine- and polyamine-free medium cellular putrescine and spermidine are rapidly depleted while the concentration of spermine decreases only moderately. We show further that the cells are able to grow in serum-containing medium without added ornithine or polyamines. This is explained by our finding that serum contains arginase which synthesizes ornithine from arginine in the medium. All the sera from different animal species tested contained arginase activity although in greatly varying amounts. Serum-free medium is therefore essential for expression of arginase deficiency in cells in tissue culture. The eventual importance of polyamines for serum-free cultures in general is discussed. 相似文献
49.
Developmental Changes in Glycolipid Synthesizing Enzymes in the Brain of a Myelin-Deficient Mutant Wistar Rat 总被引:2,自引:1,他引:1
Changes in the activities of UDP-galactose:ceramide galactosyltransferase (CGalT, EC 2.4.1.45), UDP-glucose:ceramide glucosyltransferase (CGlcT, EC 2.4.1.80) and 3'-phosphoadenosine-5'-phosphosulfate (PAPS): galactosylceramide 3'-sulfotransferase (EC 2.8.2.11) over the myelinating period between 12 and 25 days were studied in the brains of control and myelin-deficient rats. Although the activity of galactosyltransferase with ceramides containing hydroxy fatty acids quadrupled in normal male littermates between 14 and 20 days, hardly any increase was observed in the mutant and the activity was less than 10% of control above 20 days of age. With normal fatty acid containing ceramides as acceptors, the activity decreased from 83% of the control at 12 days to approximately 30% after 20 days. Sulfotransferase activity also did not show the normal increase during the 3rd week of life and declined from 60% to 22%. Glucosyltransferase and lysosomal hydrolases in brain and ceramide galactosyltransferase in sciatic nerves appeared to be normal. These results suggest close similarities to the jimpy mutant mouse in which myelin deficiency is also inherited as an x-linked recessive trait. 相似文献
50.
Zinc deficiency in wetland rice along a toposequence of hydromorphic soils in the Philippines 总被引:1,自引:1,他引:0
Summary Zinc deficiency in rice induced by prolonged water saturation of the soil is widespread in the Philippines. The poor drainage associated with the disorder is mostly due to upwelling of shallow artesian water in footslope areas and to ponding of water from continually flowing artesian wells common in such areas. One toposequence where no Zn deficiency occurred in the highest field and progressively severe Zn deficiency in successive lower fields, was studied in detail. With lower elevation soils showed an increase in organic matter and free carbonate, associated with increased upwelling and ponding of artesian water very high in dissolved Mg and Ca bicarbonate. 相似文献