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1.
2.
Determination was made of the proportion of selected by-products (acetaldehyde, ethyl acetate, methanol, propanol, isobutanol, 2-methyl-butanol, 3-methyl-butanol) of batch and continuous ethanol fermentation carried out with the use of yeastSaccharomyces cerevisiae, strain 0–11, cells immobilized by adsorption on selected carriers (foamed polystyrene, bone shot, beech wood chips, porous glass) as well as by entrapping in calcium alginate and calcium pectinate gel. 相似文献
3.
High Performance Liquid Chromatography of Molecular Species from Free Sterols and Sterylglycosides Isolated from Oat Leaves and Seeds 总被引:1,自引:0,他引:1
Free sterols and sterylglycosides (SG) from oat leaves and seedswere isolated by conventional thin layer chromatography (TLC)and subjected to high performance liquid chromatography (HPLC)for resolution of molecular species. Acylsterylglycosides, isolatedby TLC, were converted to SG by mild alkaline hydrolysis anddetermined as SG. Sterols and SG were injected onto the columnwithout any chemical treatment and the separated species weredetected at 200 nm. The separation of SG-species follows exactlythe separation of free sterols. Though gas liquid chromatography still is the method of choice,advantages of HPLC is to analyse directly the SG-species withouthydrolysis and derivatization as compared to GLC. After TLCthe sterol- and the SG-fraction are injected directly onto thecolumn. This is extremely important for labile sterylglycosidesor sterols, as demonstrated for the avenasterols.
1 Preliminary reports have been presented on the "4. Arbeitstagung,Pflanzliche Lipide", October 78, 1983 in M?nster (FRG)and on the "6th International Symposium on the Structure, Functionand Metabolism of Plant Lipids", Neuchatel, Switzerland, July1620, 1984. (Received November 12, 1984; Accepted January 14, 1985) 相似文献
4.
Zusammenfassung Regionale und artliche Unterschiede der Rückstände von Quecksilber in Eiern von sieben Brutvogelarten der deutschen Nordseeküste wurden untersucht. Bei vier Arten stellten wir deutliche geographische Unterschiede in der Kontamination fest (Abb. 1). Höchstgehalte fanden wir in Eiern von der Elbmündung (Region V). Austernfischer- und Flußseeschwalbeneier von der inneren Deutschen Bucht (Region VI) enthielten größere Mengen als solche von Nordfriesland (Region VII). Der gesetzliche Richtwert für Eier (0,03 mg/kg) wurde von 353 der 355 untersuchten Eier überschritten. Fluß- und Brandseeschwalbe waren am stärksten, Brandgans, Austernfischer und Lachmöwe am wenigsten mit Quecksilber kontaminiert (Abb. 2, 4.2.). Mit Ausnahme von Brandgans und Silbermöwe erreichten die Rückstände in vielen Eiern der anderen Arten, an der Elbe sogar in allen Eiern, eine den Bruterfolg gefährdende Größenordnung, insbesondere bei der Flußseeschwalbe.
Pollutants in eggs of birds breeding at the German North Sea Coast. II. Mercury
Summary Regional and interspecific differences of mercury residues were investigated in the eggs of seven species breeding at the German North Sea Coast (Tadorna tadorna, Haematopus ostralegus, Charadrius hiaticula, Larus argentatus, L. ridibundus, Sterna hirundo, S. sandvicensis). We found distinct geographical differences in contamination (Fig. 1): In eggs from the Elbe Eastuary (region V) maximum residues of mercury were ascertained. Eggs of Oystercatcher and Common Tern from the Bay of Helgoland (region VI) contained larger quantities than eggs from Northern Frisia (region VII). 353 from 355 eggs examined showed a value exceeding the legal standard value for eggs which is 0,03 mg/kg in Germany. Common Tern and Sandwich Tern eggs had the highest, Shelduck, Oystercatcher and Blackheaded Gull eggs the lowest mercury contamination (Fig. 2, 4.2.). With the exception of Shelduck and Herring Gull, residues in many eggs of the other species — at the river Elbe in all eggs — came up to a range endangering breeding success, especially in Common Terns.相似文献
5.
DNA-dependent in vitro synthesis of enzymes of the galactose operon of Escherichia coli 总被引:19,自引:0,他引:19
Summary Two active enzymes of the galactose operon of Escherichia coli, uridyl transferase and galactokinase have been synthesized with high yields in a DNA dependent system for protein synthesis. The unspecific blank values amount to less than two percent of the rate obtained under optimal conditions and permit the accurate determination of even a small fraction of the maximum synthesis rate. Therefore this system provides a sensitive assay for the biological activity of DNA that contains the intact galactose operon of Escherichia coli.The synthesis of these galactose enzymes is to a high extent dependent on the presence of cyclic adenosine-3:5-monophosphate.D-fucose, known as an inducer of the galactose operon in vivo, stimulates the synthesis of galactokinase, indicating that the repressor of the galactose operon in active under these conditions. This stimulation is not observed, if the bacterial extract is prepared from a strain defective for the galactose repressor or if the DNA carries an operator constitutive mutation in the galactose operon. Therefore the stimulation by D-fucose is true derepression. 相似文献
6.
Sporophytes of Ectocarpus siliculosus (Dillwyn) Lyngbye and E. fasciculatus Harvey were collected in the vicinity of Roscoff Brittany, France. Gametophytes derived from meiospores were used for intra- and interspecific crosses. Intraspecific gamete combinations gave viable zygotes, which developed into fertile sporophytes. Interspecific crosses were unsuccessful. Gamete fusions did not occur between female gametes of E. fasciculatus and male gametes of E. siliculosus. Hybrid zygotes were formed in the reciprocal combination but died soon after germination. We conclude that the two species of Ectocarpus at Roscoff represent distinct taxonomic entities, which are separated by pre- and postzygotic compatibility barriers. These biological findings are confirmed by the differential occurrence of the chemotaxonomic marker betaine-lipid diacetylglycerylhydroxymethyltrimethyl-β-alanine, which is present in our cultures of E. fasciculatus but absent in E. siliculosus. 相似文献
7.
Waldemar Lernhardt Jan Andersson Antonio Coutinho Fritz Melchers 《Experimental cell research》1978,111(2):309-316
Addition of 3 × 106 thymus cells from either syngeneic, allogeneic or xenogeneic animals increases the cloning efficiencies of murine thymomas (EL-4, WC-2), B-lymphomas (McPC 1748, 38C-13), Abelson-virus transformed cell lines (F and K), mastocytomas (P815), myelomas (AbPC22, X63-AG8, 5563, MOPC 104 E, RFC 5, W 3469) and hybrids of myelomas and normal B-lymphocytes (Sp-1), all adapted to tissue culture, to near 100%. Thymus cells also increase the efficiencies of growth initiation in primary in vitro cultures of myeloma tumor cells (S117) transplanted in vivo, and of cells fused between the azaguanine-resistant X63-AG8 myeloma cell line and normal, LPS-stimulated B-lymphocyte blasts. 相似文献
8.
Waldemar Adam Zoltan Lukacs Claudia Kahle Chantu R. Saha-Mller Peter Schreier 《Journal of Molecular Catalysis .B, Enzymatic》2001,11(4-6):377-385
Screening of soil bacteria with allylbenzene resulted in a Bacillus megaterium strain, which hydroxylates simple hydrocarbons in high enantiomeric excess (ee up to 99%). Benzylic and nonbenzylic hydroxylation products were obtained, without the usually observed high preference for the benzylic position. The immobilization of the B. megaterium cells in alginate gel effectively improved the stability of the cells and increased the amounts of products formed, without loss of enantioselectivity. The product ratio ( vs. β hydroxylation) was shifted towards benzylic hydroxylation, which suggests that at least two hydroxylating enzymes with distinct regioselectivity are involved. Comparison to free-cell fermentations in small- and large-scale bioreactors (up to 2000 ml) showed that the use of immobilized cells is advantageous, as they are easier to handle and yield higher amounts of oxidation products. 相似文献
9.
Joshua A. F. Sutton Oliver T. Carnell Lucia Lafage Joe Gray Jacob Biboy Josie F. Gibson Eric J. G. Pollitt Simone C. Tazoll William Turnbull Natalia H. Hajdamowicz Bartomiej Salamaga Grace R. Pidwill Alison M. Condliffe Stephen A. Renshaw Waldemar Vollmer Simon J. Foster 《PLoS pathogens》2021,17(3)
Peptidoglycan is the major structural component of the Staphylococcus aureus cell wall, in which it maintains cellular integrity, is the interface with the host, and its synthesis is targeted by some of the most crucial antibiotics developed. Despite this importance, and the wealth of data from in vitro studies, we do not understand the structure and dynamics of peptidoglycan during infection. In this study we have developed methods to harvest bacteria from an active infection in order to purify cell walls for biochemical analysis ex vivo. Isolated ex vivo bacterial cells are smaller than those actively growing in vitro, with thickened cell walls and reduced peptidoglycan crosslinking, similar to that of stationary phase cells. These features suggested a role for specific peptidoglycan homeostatic mechanisms in disease. As S. aureus missing penicillin binding protein 4 (PBP4) has reduced peptidoglycan crosslinking in vitro its role during infection was established. Loss of PBP4 resulted in an increased recovery of S. aureus from the livers of infected mice, which coincided with enhanced fitness within murine and human macrophages. Thicker cell walls correlate with reduced activity of peptidoglycan hydrolases. S. aureus has a family of 4 putative glucosaminidases, that are collectively crucial for growth. Loss of the major enzyme SagB, led to attenuation during murine infection and reduced survival in human macrophages. However, loss of the other three enzymes Atl, SagA and ScaH resulted in clustering dependent attenuation, in a zebrafish embryo, but not a murine, model of infection. A combination of pbp4 and sagB deficiencies resulted in a restoration of parental virulence. Our results, demonstrate the importance of appropriate cell wall structure and dynamics during pathogenesis, providing new insight to the mechanisms of disease. 相似文献
10.
Constantin N. Takacs Jason Hocking Matthew T. Cabeen Nhat Khai Bui Sebastian Poggio Waldemar Vollmer Christine Jacobs-Wagner 《PloS one》2013,8(2)
The peptidoglycan (PG) is a macromolecular component of the bacterial cell wall that maintains the shape and integrity of the cell. The PG of Caulobacter crescentus, unlike that of many other Gram-negative bacteria, has repeatedly been shown to contain significant amounts of glycine. This compositional peculiarity has been deemed an intrinsic characteristic of this species. By performing a comprehensive qualitative and quantitative analysis of the C. crescentus PG by high-performance liquid chromatography (HPLC) and mass spectrometry (MS), we show here that glycine incorporation into the C. crescentus PG depends on the presence of exogenous glycine in the growth medium. High levels of glycine were detected at the fifth position of the peptide side chains of PG isolated from C. crescentus cells grown in the complex laboratory medium PYE or in defined medium (M2G) supplemented with casamino acids or glycine alone. In contrast, glycine incorporation was undetectable when cells were grown in M2G medium lacking glycine. Remarkably, glycine incorporation into C. crescentus peptidoglycan occurred even in the presence of low millimolar to sub-millimolar concentrations of free glycine. High glycine content in the PG had no obvious effects on growth rates, mode of PG incorporation or cell morphology. Hence, the C. crescentus PG is able to retain its physiological functions in cell growth and morphogenesis despite significant alterations in its composition, in what we deem to be unprecedented plasticity. 相似文献