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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    FEMS microbiology letters 152 (1997), S. 0 
    ISSN: 1574-6968
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Cosmid-borne and chromosomal lacZ fusions to aapJ, aapQ and aapM were used to examine the nitrogen regulation of the general amino acid permease (Aap) of Rhizobium leguminosarum strain 3841. Transcription of the first gene of the operon (aapJ), which encodes the periplasmic binding protein, was 2–4-fold higher than aapQ and aapM, which encode the integral membrane proteins, under various growth conditions. This may be due to the presence of a putative stem loop in the intergenic region between aapJ and aapQ. All aap fusions were derepressed 3–5-fold after growth on glutamate as a nitrogen source, which effectively causes nitrogen limitation. An ntrC mutant was derepressed for transcription of the aap operon and had high rates of amino acid transport when grown on ammonia as the nitrogen source. Thus NtrC negatively regulates the aap operon, contrary to its usual role in positive gene activation. These results confirm that the aap operon is subject to complex regulation involving both transcriptional and post-transcriptional factors.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Molecular microbiology 21 (1996), S. 0 
    ISSN: 1365-2958
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology , Medicine
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1432-072X
    Keywords: Key words Phosphatases ; Citrobacter ; Acid ; phosphatase ; Phosphatase isoforms
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract An acid phosphatase from a heavy-metal-accumulating strain of a Citrobacter sp. was resolved into two forms on the basis of their nonbinding (phosphatase I) or binding (phosphatase II) behaviour on the cation-exchange resin SP-Sephadex C50. Both holoenzymes had a molecular mass of 103–108 kDa as determined by Superose Q-6 column chromatography in the presence of 150 mM KCl and a subunit molecular mass of 27 kDa as determined by SDS-PAGE; the enzyme was tetrameric. Both enzymes had a pI ≈ 9.0 and were immunologically cross-reactive. There were minor differences in amino acid composition and in peptide maps following tryptic digest. The pH optimum for phosphatases I and II was 5.5 and 6.25, respectively; phosphatase II alone retained activity at pH values up to 9.0. Phosphatase I was more resistant to mechanical shear, γ-irradiation, high temperature, and toxins (F– and formaldehyde). Glycerol increased the thermostability of both enzymes, particularly the more thermosensitive phosphatase II. Phosphatase II had a lower K m and a lower V max for glycerol 2-phosphate hydrolysis. The production of enzyme isoforms is a phenomenon similar to that described previously for the alkaline phosphatase of Escherichia coli, where the isoforms relate to precursive and final processed forms of the enzyme. Acid phosphatase is physiologically distinct, with a role that is still obscure but that may relate to cellular stress responses.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Archives of microbiology 153 (1990), S. 368-372 
    ISSN: 1432-072X
    Keywords: Bacterial chemotaxis ; Nutrient-limitation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Rhodobacter sphaeroides, which lacks methyl accepting chemotaxis proteins, showed a strong response to gradients of either pyruvate or propionate. If cells were placed in a saturating background of pyruvate they no longer responded to a gradient of propionate but they still responded to potassium or ammonia. This demonstrates that pyruvate saturated the response to another carbon source, but not to other classes of compound. The total movement of cells in a pyruvate background was maintained at a high level relative to a buffer control, indicating an apparent lack of adaptation to saturating pyruvate. The response of R. sphaeroides to a saturating background of pyruvate was weak in cells grown on limiting ammonia although these cells showed a strong response to ammonia. These data suggest that cells show a strong response to the class of compound that currently limits motility. Two hypotheses to explain these results are presented. Firstly, cells show a chemotactic response to a gradient of the limiting compound until saturated by it, they then respond to a gradient of the new compound that has then become limiting. The chemotactic response is the result of a decrease in stopping frequency as cells move up a gradient and an increase as they move down. Secondly, the behavioural response may have two components, a short term chemotactic response and a long term excitation of motility.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1432-072X
    Keywords: Motility ; Chemotaxis ; Rhodobacter sphaeroides ; Membrane potential ; Electron transport
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The effect of the chemoattractants acetate, propionate, pyruvate and potassium on the steady state membrane potential and the rate of respiratory electron transport was examined in Rhodobacter sphaeroides. Under conditions where the membrane potential makes up most of the proton motive force, all attractants increased the steady state membrane potential in the dark. However, only potassium was able to consistently increase the steady state membrane potential in the light. All of the attractants were able to increase the mean swimming speed of cells at high light levels for prolonged periods, showing that the increase in mean speed cannot be caused by an increase in the membrane potential. Measurement of chemotaxis in wells showed a positive response to propionate in the dark, at low light (10 – 20 μmol photons m−2 s−1) and in high light (700 μmol photons m−2 s−1). The demonstration of chemotaxis in the dark precluded any direct role of photosynthetic electron transport in chemotaxis. The response at high light, where there was no induced change in membrane potential, confirmed that the steady state membrane potential was not involved in tactic signalling. Acetate, propionate and pyruvate at appropriate concentrations stimulated the rate of respiratory electron transport in the dark, while potassium had no effect. In low light, all three organic acids caused a significant stimulation of respiratory electron transport but potassium caused a significant inhibition. In high light, only pyruvate and propionate caused a significant increase in the rate of respiratory electron transport. Chemoattractants can therefore produce a significant positive tactic response when respiratory electron transport is either unaffected or inhibited. These data show that neither a change in the bulk steady state membrane potential nor the rate of respiratory electron transport causes either the change in swimming behaviour or acts as a chemotactic signal.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Biotechnology letters 22 (2000), S. 887-892 
    ISSN: 1573-6776
    Keywords: biomechanical force ; microdissection ; micromanipulation ; optical trap
    Source: Springer Online Journal Archives 1860-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract Optical traps exploit the radiation forces of laser light to manipulate microscopic particles. The ability to manipulate biological material and quantify the force required has been exploited in the biosciences; from the isolation of single cells to kinetic measurements of single motor molecules. This review describes the theory of optical trapping and using recent publications gives examples of how it has been employed across a broad spectrum of biological research.
    Type of Medium: Electronic Resource
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