Young cells produced in LK sheep during rapid hematopoiesis after massive hemorrhage contain more K than the cells which are normally released into the circulation. The K content in these new cells falls to that characteristic of mature LK cells after a few days in the circulation. K transport properties in young and old cells before and after massive bleeding were studied. Young and old cells were separated by means of a density gradient centrifugation technique. Evidence showing that younger cells are found in the lower density fractions is presented. Active transport of K in the lightest fraction as measured by strophanthidin-sensitive influx was four to five times greater in red cells drawn 6 days after massive bleeding while the K leak as measured by strophanthidin-insensitive influx was only slightly larger. No change after bleeding was observed in older cells which had been present in the circulation prior to the hemorrhage. It is concluded that the high K content of young cells produced in LK sheep after bleeding is due to temporary retention of membrane K transport properties characteristic of HK cells. Thus, genetically determined modification of membrane transport properties has been shown to occur in nondividing circulating red cells. 相似文献
The HindIII RFLP in the human phenylalanine hydroxylase (PAH) gene is caused by the presence of an AT-rich (70%) minisatellite region. This region contains various multiple of 30-bp tandem repeats and is located 3 kb downstream of the final exon of the gene. PCR-mediated amplification of this region from haplotyped PAH chromosomes indicates that the previously reported 4.0-kb HindIII allele contains three of these repeats, while the 4.4-kb HindIII allele contains 12 of these repeats. The 4.2-kb HindIII fragment can contain six, seven, eight, or nine copies of this repeat. These variations permit more detailed analysis of mutant haplotypes 1, 5, 6, and, possibly, others. Kindred analysis in phenylketonuria families demonstrates Mendelian segregation of these VNTR alleles, as well as associations between these alleles and certain PAH mutations. The R261Q mutation, associated with haplotype 1, is associated almost exclusively with an allele containing eight repeats; the R408W mutation, when occurring on a haplotype 1 background, may also be associated with the eight-repeat VNTR allele. Other PAH mutations associated with haplotype 1, R252W and P281L, do not appear to segregate with specific VNTR alleles. The IVS-10 mutation, when associated with haplotype 6, is associated exclusively with an allele containing seven repeats. The combined use of this VNTR system and the existing RFLP haplotype system will increase the performance of prenatal diagnostic tests based on haplotype analysis. In addition, this VNTR may prove useful in studies concerning the origins and distributions of PAH mutations in different human populations. 相似文献
Tilapia serum was acidified with 0.5 M HCl and then chromatographed on an octadecasily-silica column. After washing with 4% acetic acid, the column was eluted with methanol. The eluate was evaporated to dryness. The sample cross-reacted in a human insulin-like growth factor I (IGF-I) radioimmunoassay, suggesting immunochemical similarity to human IGF-I. IGF-I-like immunoreactivity was present at high levels in tilapia liver. Other tissues containing IGF-I-like immunoreactivity included the gonad, kidney, heart, spleen, brain and muscle. The serum IGF-I-like immunoreactivity was attributed to substances with a molecular weight of 9,000 and 45,000 respectively, and it was elevated after treatment with bovine growth hormone and carp pituitary extract. 相似文献
Glucocerebrosidase was purified from human cultured dermal fibroblasts more than 2200-fold to apparent homogeneity using high performance Alkyl-Superose HR 5/5 hydrophobic interaction and Bio-Sil TSK-250 gel permeation column chromatography. Sodium dodecyl sulfate--polyacrylamide gel electrophoresis and protein staining of the catalytically active and concentrated enzyme fractions from the gel permeation columns revealed the presence of one band of Mr 64,000. The glucocerebrosidase preparation purified to homogeneity was digested with peptide N-glycosidase F that cleaves N-linked oligosaccharide structures from glycoproteins. The molecular weight of glucocerebrosidase after digestion with peptide N-glycosidase F was reduced to Mr 57,000, suggesting that the mature enzyme is a glycoprotein and that N-linked oligosaccharide constitutes a minimum of about 10% of the total molecular weight of the polypeptide. These findings are compatible with the hypothesis that glucocerebrosidase was initially synthesized as a precursor polypeptide which was subsequently glycosylated to become the mature enzyme. 相似文献
Summary Economical light energy supply plays a key role in determining the success of industrial application of photosynthetic microorganisms. The bacteriochlorophyll a of C. thiosulfatophilum harvests the light at 760 nm, which oxidizes toxic H2S by photosynthesis. Light emitting diode(LED), which emits a maximum intensity at 710 nm and 60% of its maximum at 760 nm, was adopted as an alternative light source to inefficient incandescent light. With the array of the LEDs adjustable to the reactor wall 95% of the light energy was saved over the incandescent light source in comparable conditions. 相似文献
A quasilinear viscoelastic model was used to develop relaxation and creep forms for a constitutive law for soft tissues. Combined relaxation and cyclic test data as well as preconditioned and nonpreconditioned creep data were used to demonstrate the approach for normal bovine articular cartilage. Values for mechanical parameters in the analytical models were determined using a generalized least squares method. 相似文献
1. 1.|The metabolic role of the thyroid gland was studied in intact snakes, Naja naja and Ptyas korros treated with tri-iodo-thyronine (T3) and thyroxine (T4) and in thyroidectomized (Tx) N. naja kept at 21°C by analyzing tissue composition and glycogen phosphorylase a activity.
2. 2.|Liver weight was unaffected by thyroid hormone injection in both species but decreases in liver glycogen followed T3 or T4 injection, and there was an increase in liver glycogen in N. naja. These changes in liver glycogen were accompanied by a decrease in glycogen phosphorylase a activity with T3 injection. T3 decreased muscle glycogen in Ptyas and Tx increased it in N. naja.
3. 3.|T3 increased % liver lipid in Ptyas but not in Naja.
4. 4.|Between species, there were differences in liver weight, blood glucose level, cholesterol level and % muscle lipid.
5. 5.|The results showed that thyroid hormones affected carbohydrate and lipid metabolism at a low temperature of 21°C, although the significance is not known.
A novel restriction fragment length polymorphism in the phenylalanine hydroxylase (PAH) locus generated by the restriction endonuclease MspI was observed in a German phenylketonuria (PKU) patient. Molecular cloning and DNA sequence analyses revealed that the MspI polymorphism was created by a T to C transition in exon 9 of the human PAH gene, which also resulted in the conversion of a leucine codon to a proline codon. The effect of the amino acid substitution was investigated by creating a corresponding mutation in a full-length human PAH cDNA by site-directed mutagenesis followed by expression analysis in cultured mammalian cells. Results demonstrate that the mutation in the gene causes the synthesis of an unstable protein in the cell corresponding to a CRM- phenotype. Together with the other mutations recently reported in the PAH gene, the data support previous biochemical and clinical observations that PKU is a heterogeneous disorder at the gene level. 相似文献