The fractional precipitation of soil humic acid by ammonium sulphate

Summary A number of fractions have been obtained from a soil humic acid by salting-out and by leaching with ammonium sulphate. The fractions obtained are characterised by infra-red and ultra-violet spectroscopy and osmometry. The fractions removed at relatively low saturation with ammonium sulphate are less highly charged and contain more aliphatic hydrocarbon groups per unit weight than the fractions precipitated at high concentrations of salt. In addition, the number average molecular weight of successive fractions precipitated with ammonium sulphate decreases significantly.     

Studies on the proteins of Poekilocerus pictus. II--changes taking place in the haemolymph protein during maturation of female

In all, 7 protein fractions have been detected in the haemolymph of Poekilocerus pictus by the polyacrylamide gel disc electrophoresis. Out of seven protein fractions, four fractions i.e.3,4,5 and 6 take major role in the vitellogenesis. These fractions are accumulated in the ovariectomised female insect. No yolk is deposited in the allatectomised female ovary. The protein fractions 4, 5 and 6 show high concentration of protein in the allatectomised female as compared to the show operated female. It is concluded that the synthesis of protein fraction 3 is controlled by the corpora allata while the fractions 4, 5 and 6 are controlled by the neurosecretory cells.     

Heterogeneity and Heterofunctionality of Hemoglobins in Bloodworms (Diptera, Chironomidae)

In electrophoretic spectra of hemoglobins of Chironomus species of plumosus group, 3 groups of fractions are arbitrarily identified: fast fractions (mobility of 0.85 and higher), fractions with intermediate mobility (0.58–0.83), and slow fractions (mobility of 0.43 and lower). The most unstable turned out to be the fast fractions; their protein content increased considerably at storage and repeated freezing–thawing of samples. Fractions with the intermediate mobility are the most numerous, have a high specific amount according to the protein content and a high peroxidase activity. The slow fractions in the majority of species were characterized by a low peroxidase activity and high protein content. An interspecies comparison of electrophoretic spectra of hemoglobins has shown that the species that are the most tolerant to oxygen deficiency have the slow fractions with the lowest mobility. The obtained data have allowed suggesting that that the identified groups of hemoglobins are functionally heterogeneous: (1) the fast fractions with mobility of 0.85 and higher are products of degradation of hemoglobins with a higher molecular mass; (2) fractions with intermediate mobility (0.58–0.83) have a high affinity to oxygen and provide its utilization at its very low concentrations in water; (3) the slow fractions with mobility of 0.43 and lower have a high mol. mass and perform the buffer function preventing disturbance of the acid-base equilibrium of internal medium at anaerobiosis.     

Distribution of Calretinin, Calbindin D28k, and Parvalbumin in Subcellular Fractions of Rat Cerebellum: Effects of Calcium

Abstract: The distribution of calretinin, calbindin D28k, and parvalbumin was examined in subcellular fractions prepared from rat cerebellum and analyzed by immunoblot. Calretinin was also quantified by radioimmunoassay. As expected, all three soluble, EF-hand calcium-binding proteins were predominantly localized in the cytosolic fraction. Calretinin and calbindin D28k were also detected in membrane fractions. Calretinin was more abundant in synaptic membrane than in microsomal fractions. The cerebellar microsomal fraction contained the greatest concentration of membrane-associated calbindin D28k. The association of calretinin and calbindin D28k with membrane fractions was decreased in samples prepared or incubated in low calcium. Quantification of calretinin in subcellular fractions of rat cerebellum revealed a greater amount of calretinin in cytosolic fractions prepared or incubated in low calcium and reduced amounts of calretinin in all membrane fractions incubated in low calcium with the exception of the mitochondrial fraction. These results imply that calretinin and calbindin D28k might have physiological target molecules that are associated with, or are components of, brain membranes.     

Purification of plasma membrane fractions from the bovine pars intermedia and neurohypophyseal lobe and properties of associated adenylate cyclase.

A procedure for the isolation of plasma-membrane-enriched fractions from bovine 'pars intermedia' and neurohypophysis is described. Various fractions are isolated by differential centrifugation and discontinuous sucrose density gradients. The plasma-membrane-enriched fractions have a density in sucrose of 1.14 and 1.16 and the yields are 1.8 mg and 1.5 mg per gram of tissue for the pars intermedia and neural lobe, respectively. The fractions are characterized by electron microscopy and enzymatic assays. The plasma membrane fractions are mainly vesicular in nature and are free of nuclei, mitochondria, and microsomes when examined by electron microscopy. 5'-Nucleotidase (EC 3.1.3.5) and Mg2+-(Na+ + K+)-ATPase (EC 3.6.1.3) activities are concentrated in the plasma-membrane-enriched fraction. Also, adenylate cyclase (EC 4.61.1) shows a 5 to 10-fold purification in the isolated membrane fraction. NaF (10mM) gives a two to three-fold stimulation of enzymatic activity in all fractions studied The yields of adenylate cyclase, 5'-nucleotidase, and Mg2+-(Na+ +K+)-ATPase are about 6% in the membrane fraction.     

Studies on proteins of animal ribosomes

Summary Total ribosomal protein from rat liver ribosomes can be separated into about 20 chief electrophoretic fractions by preparative polyacrylamide gel electrophoresis. Ten electrophoretically homogeneous fractions have been isolated from the total mixture of ribosomal protein, respectively from proteins, prefractionated by CM-cellulose chromatography. Amino acid composition and molecular weights of some fractions have been determined. The amino acid composition of these fractions and of the total protein mixture are basically similar but there are also significant differences with regard to some amino acids. The molecular weights of the proteins studied are in the range between 7,000 and 29,000.     

Amino acid composition and affinity to oxygen of domestic duck hemoglobins

The method of disk-electrophoresis in PAAG has shown that hemoglobin of domestic ducks is heterogeneous and consists of four electrophoretically homogeneous fractions: two fractions with high content of protein and two minor fractions. They differ in the content of lysine, histidine, serine, glycine, glutamic acid, tyrosine and phenyl alanine as well as in affinity to molecular oxygen. The minor fractions are characterized by low and high affinity to oxygen and fractions with high content of protein occupy an intermediate position.     

Ivermectin resistant and susceptible third-stage larvae of Haemonchus contortus: cholinesterase and phosphatase activities

Cholinesterase and acid phosphatase (AP), but not alkaline phosphatase activities, were detected in cytosolic and membrane-bound fractions of ivermectin resistant and susceptible Haemonchus contortus infective-stage larvae. Some differences in acetylcholinesterase activity of cytosolic fractions and in the AP activity of these fractions as well as in the response to AP inhibitors by membrane-bound fractions were detected. Data are discussed.     

Studies on proinsulin and proglucagon biosynthesis and conversion at the subcellular level: I. Fractionation procedure and characterization of the subcellular fractions

Anglerfish islets were homogenized in 0.25 M sucrose and separated into seven separate subcellular fractions by differential and discontinuous density gradient centrifugation. The objective was to isolate microsomes and secretory granules in a highly purified state. The fractions were characterized by electron microscopy and chemical analyses. Each fraction was assayed for its content of protein, RNA, DNA, immunoreactive insulin (IRI), and immunoreactive glucagon (IRG). Ultrastructural examination showed that two of the seven subcellular fractions contain primarily mitochondria, and that two others consist almost exclusively of secretory granules. A fifth fraction contains rough and smooth microsomal vesicles. The remaining two fractions are the cell supernate and the nuclei and cell debris. The content of DNA and RNA in all fractions is consistent with the observed ultrastructure. More than 82 percent of the total cellular IRI and 89(percent) of the total cellular IRG are found in the fractions of secretory granules. The combined fractions of secretory granules and microsomes consistently yield >93 percent of the total IRG. These results indicate that the fractionation procedure employed yields fractions of microsomes and secretory granules that contain nearly all the immunoassayable insulin and glucagons found in whole islet tissue. These fractions are thus considered suitable for study of proinsulin and proglucagon biosynthesis and their metabolic conversion at the subcellular level.     

Multidimensional proteomics of human serum using parallel chromatography of native constituents and microplate technology

A versatile, multidimensional, and non-denaturing proteome separation procedure using microplate technology is presented, yielding a digitized image of proteome composition. In the first dimension, the sample under study is separated into 96 fractions by size exclusion chromatography (SEC). In the second dimension, the fractions of the first dimension are transferred by the liquid-handling device CyBi-Well (CyBio AG, Jena, Germany) to 96 parallel anion exchange chromatography columns. In this way the proteins are conserved in their native states and are distributed in 2400 liquid fractions with high recovery rates and sufficient reproducibility. The resulting fractions are subjected to protein quantitation and identification. Spectrophotometrical and immunological methods and enzyme activity measurements are used for quantitation. To identify proteins, the fractions are subjected to MALDI-MS, and their tryptic digests to both MALDI- and LC-ESI-MS/MS. All preparation steps except the first are applied in parallel to sets of multiples of 96 samples. The procedure may be refined by adding more separation steps and may be adapted to various protein amounts and to various proteomes. Moreover, the method offers the opportunity to investigate functional protein complexes. The method was applied to separate the normal human serum proteome. Within 255 fractions exhibiting the highest protein concentrations, 742 proteins were identified by LC-ESI-MS/MS peptide sequence tags.     

Comparative studies of fresh and postmortem isolated rat cortical synaptosomes: uptake and potassium-evoked release of gamma-aminobutyric acid

Synaptosomal fractions were isolated from rat cerebral cortex immediately after decapitation and after 2 h and 4 h postmortem storage at room temperature. Uptake and release of [3H]GABA was compared between fresh and postmortem synaptosomal fractions. The results suggest that after a 2 h postmortem storage these functions are still comparable to those observed in fresh preparations, while a 4 h period of storage decreases them by about 50%. The present data are consistent with our previous findings that the 2 h postmortem fractions are comparable to freshly isolated fractions with respect to coupled respiration, potassium accumulation and capability of specific configurational changes.     

Content of SH-groups in some fractions of rat hemoglobin

Eight fractions of rat hemoglobin obtained by electrophoresis in polyacrylamide gel were studied. Having used parachloromercuric benzoate (PChMB) and 5,5-dithio-bis (2-nitrobenzoic acid) it was established that fractions of 3 and 3a carboxyhemoglobin contain 6 available SH-groups and the rest one (1, 2, 2a, 4, 5, 6) about 4 SH-groups. In all fractions only 2 masked SH-groups are found. A problem is discussed on SH-groups localization in the polypeptide chains of certain hemoglobin fractions in rats.     

Uptake of taurine into subcellular fractions of C-6 glioma cells.

Subcellular fractions from cultured C-6 glioma cells prepared by methods similar to those for crude synaptosomal fractions of rat cerebral cortex accumulated [³⁵S]taurine as did intact glioma cells. Thus, the accumulation of taurine was dependent on temperature and sodium concentration and sensitive to osmotic shock. The kinetic properties of this uptake are characterized by an apparent K_m, of about 25 μm, The properties of taurine uptake into subcellular fractions from C-6 glioma cells were compared with those of crude synaptosomal fractions and differences could be observed in temperature sensitivity and with metabolic inhibitors, which were less potent in the glioma preparation. Equilibrium density gradient centrifugation of subcellular fractions from glioma cells revealed that particles containing [³⁵S]taurine sediment to a lower buoyant density than mitochondria. But on co-sedimentation of subcellular fractions from glioma cells with synaptosomal fractions derived from cerebral cortex, differences in the buoyant density between these two preparations could be found. The findings support the possibility of a contamination of synaptosomal fractions with subcellular fractions derived from glial origin.     

Isoelectric spectra and peptide maps of major electrophoretically homogeneous fractions of duck hemoglobin

Differences are shown in isoelectrical spectra and peptides sets of two main electrophoretically homogeneous fractions of domesticated duck hemoglobin. The hemoglobin fractions under study are characterized by the same affinity to molecular oxygen.     

Cellular compartmentalization of protein kinase activity during the cell cycle

The quantities and types of protein kinases found in the cytoplasmic and nuclear or chromosomal compartments of interphase and mitotic human culture cells were compared. Using histone as substrate, the total quantity of kinases recovered from cytoplasmic and chromosomal fractions of mitotic cells was several times greater than from cytoplasmic and nuclear fractions of interphase cells. In both mitotic and interphase cells, more activity was recovered from cytoplasmic fractions than from chromosomal or nuclear fractions, respectively. When activity against various substrates was examined, mitotic chromosomal extracts were found to display the greatest preference for the H1 fraction of histones. Neither cytoplasmic nor chromosomal fractions from mitotic cells exhibited enhanced activity in the presence of cAMP, whereas the activity of both cytoplasmic and nuclear fractions of interphase cells was enhanced. Protein kinases, previously identified by nondenaturing polyacrylamide gel electrophoresis as present in the cytoplasmic fraction of mitotic but not interphase cells, were also present in chromosomal fractions of mitotic cells; only one of these kinases may be present in nuclear extracts of interphase cells. In addition, the profiles of nuclear extracts of interphase cells differ from their cytoplasmic fractions. These results indicate that there are protein kinases which are restricted to the mitotic phase of the cell cycle and that they apparently partition between the cytoplasmic and chromosomal compartments of cells in mitosis.     

Male accessory gland secretory proteins in nasuta subgroup of Drosophila: nature and SDS-PAGE patterns

Male accessory gland secretory proteins in seven members of Drosophila nasuta subgroup were analyzed by SDS-PAGE in combination with different staining techniques such as CBB-R250, Silver, PAS, PAS-silver and zinc-imidazole reverse staining. Based on coomassie blue patterns the protein fractions could be classified in to 3 major groups namely group I, group II as well as group III; with high molecular weight fractions falling into group I and low molecular weight fractions into group III. All the three groups of fractions are post-translationally modified by way of glycosylation and group III fractions are found to be highly glycosylated. Fractions of groups I and II when localized with silver stain and group III fractions when localized with PAS-silver stain appear yellow; suggesting that they are sialoglycoproteins. A 40 kD fraction of group II shows differential staining property with zinc-imidazole stain in closely related species namely D. n. nasuta and D. n. albomicans. Analysis of this protein fraction in F1 males of an interspecific cross revealed that it is synthesized by X-chromosomal gene.     

Comparative studies on the polypeptide composition of chloroplast lamellae and lamellar fractions

The polypeptide composition of spinach chloroplast membranes and membrane fractions has been examined by the technique of sodium dodecylsulfate-polyacrylamide gel electrophoresis. Chloroplasts were fragmented into grana (Photosystem II enriched) and stroma lamellae (Photosystem I in character) by the French press technique. The grana lamellae were futher fractionated by the use of digitonin into two fractions, one enriched in Photosystem II and the other enriched in Photosystem I. These membranes are composed of at least 15 polypeptides two of which, with approximate weights of 39 and 50 kdaltons, are observed only in granal fractions. Quantitatively the primarily Photosystem II fractions are enriched in polypeptides in the 30-23 kdalton range whereas the Photosystem I (or Photosystem I-enriched) fractions are enriched in polypeptides in the 60-54 kdalton region. The experiments reported show that contamination by soluble proteins or other membranes is negligible. The results indicate that subtle differences in composition account for the large differences in structure and function within the chloroplast membrane system.     

Studies on the sterols and sterol esters of the intracellular organelles of maize shoots

1. The composition of the esterified and unesterified sterols of the nuclear, chloroplastidic, mitochondrial and microsomal fractions of 21-day-old maize shoots was examined. 2. The microsomal and mitochondrial fractions contain the bulk of the sterols of the tissue. 3. Only 1% of the sterol isolated from all the organelles is esterified. 4. The nuclear fraction has the greatest proportion of esterified sterol and the microsomal fraction the least. 5. 4-Demethyl sterols constitute the bulk of both esterified and unesterified sterols in all organelle fractions. 6. Cholesterol is the major esterified 4-demethyl sterol of the nuclear and chloroplastidic fractions, but only the nuclear fraction has an appreciable proportion of unesterified cholesterol. 7. Sterol esters of linolenic acid are more abundant in the mitochondrial and microsomal fractions than in the other two fractions.     

Effect of Soil Organic Matter on Some Root Surface Enzymes of and Uptakes into Winter Wheat

Soil organic matter (SOM) fractions inhibit the activity ofroot invertase and phosphatase, but the extent of the inhibitiondepends on the SOM fraction. About 93% of the invertase andsome 50% of phosphatase is in the soluble cell components. Ineach case the soluble and cell wall-bound enzymes are affectedsimilarly by SOM fractions. SOM fractions are non-competitiveinhibitors of invertase activity altering only the V_max of thereaction. Sucrose has access only to some 50% of the total invertasein the intact root, which may be the root-surface invertase. All SOM fractions inhibit the uptake of glucose into roots butin general stimulate the uptake of inorganic phosphate.