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  • 1
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Archives of microbiology 127 (1980), S. 273-277 
    ISSN: 1432-072X
    Keywords: Methanobacterium thermoautotrophicum ; Methanosarcina barkeri ; Methanobrevibacter ruminantium ; Factor F430 ; Nickel ; Iron ; Cobalt ; Molybdenum
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Factor F430 is a yellow compound of unknown structure present in methanogenic bacteria. It has recently been shown to contain nickel. In this communication the influence of the nickel concentration in the growth medium on the factor F430 content of Methanobacterium thermoautotrophicum and on the nickel content of factor F430 was studied. It was found: (1) The content of factor F430 in the cells was strongly dependent on the nickel concentration of the growth medium. Cells grown on media with 2.5 μM NiCl2 contained 28 times as much factor F430 per g as those grown on media with 0.075 μM NiCl2; (2) factor F430 was synthesized in nickel deprived cells only upon the addition of nickel Nickel uptake paralleled factor F430 synthesis; (3) independent of the nickel concentration in the growth medium, the extinction coefficient at 430 nm of factor F430 per mol nickel was always near 22,500 cm-1 (mol Ni)-1. These findings indicate that nickel is an essential component of factor F430.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Archives of microbiology 138 (1984), S. 224-228 
    ISSN: 1432-072X
    Keywords: CO2 reduction to acetate ; Clostridium thermoaceticum ; Acetobacterium woodii ; Carbon monoxide dehydrogenase ; Carbon monoxide fixation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Cultures of Acetobacterium woodii and Clostridium thermoaceticum growing on fructose or glucose, respectively, were found to produce small, but significant amounts of carbon monoxide. In the gas phase of the cultures up to 53 ppm CO were determined. The carbon monoxide production was completely inhibited by 1 mM cyanide. Cultures and cell suspensions of both acetogens incorporated 14CO specifically into the carboxyl group of acetate. This CO fixation into C1 of acetate was unaffected by cyanide (1 mM). The findings are taken to indicate that CO (in a bound form) is the physiological precursor of the C1 of acetate in acetate synthesis from CO2. The cyanide inhibition experiments support the hypothesis that the cyanide-sensitive carbon monoxide dehydrogenase may serve to reduce CO2 to CO rather than to incorporate the carbonyl into C1 of acetate.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Archives of microbiology 144 (1986), S. 386-392 
    ISSN: 1432-072X
    Keywords: CO formation from CO2 ; CO2 reduction to acetate ; Actetate formation from CO and formaldehyde ; Carbon monoxide oxidation ; Acetobacterium woodii ; Proton motive force ; ATP synthesis ; Amino acid transport
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Cell suspensions of Acetobacterium woodii produced CO from H2 and CO2. Depending on the conditions, more than 1,000 ppm CO were measured in the gas phase. This concentration was more than 10-fold higher than the thermodynamic equilibrium concentration that can be calculated to be 83.5 ppm for the experimental conditions used. This finding is taken as evidence that, besides the activation of formate, also CO production from CO2 is an energy-dependent step in the reduction of CO2 to acetate. Studies on the influence of ionophores and dicyclohexylcarbodiimide (DCCD) as well as that of CO and formaldehyde on acetate synthesis were undertaken in order to determine whether ATP or $$\Delta \tilde \mu _H $$ is the driving for CO2 reduction to CO. Cells of A. woodii also catalyzed the conversion of CO (5% in the gas phase) to CO2 and H2. This process was coupled to the generation of metabolic energy, which could be used by the cells to drive the uptake of histidine into the cells; histidine uptake was almost completely inhibited by the ionophores valinomycin plus nigericin. The data were taken to indicate that in this acetogen the energy derived from CO oxidation can be converted to metabolic energy.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1432-072X
    Keywords: Anaerobic dehalogenation ; Reductive dechlorination ; Perchloroethylene ; Tetrachloroethene ; Tetrachloroethene respiration ; cis-1,2-Dichloroethene ; Trichloroethene ; Dehalospirillum multivorans
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract A strictly anaerobic bacterium dechlorinating tetrachloroethene (perchloroethylene, PCE) via trichloroethene (TCE) to cis-1,2-dichloroethene (DCE) was isolated from activated sludge with pyruvate plus PCE as energy substrates. The organism, called Dehalospirillum multivorans, is a gram-negative spirillum that does not form spores. The G+C content of the DNA was 41.5 mol%. According to 16S rRNA gene sequence analysis, D. multivorans represents a new genus and a new species belonging to the epsilon subdivision of Proteobacteria. Quinones, cytochromes b and c, and corrinoids were extracted from the cells. D. multivorans grew in defined medium with PCE and H2 as sole energy sources and acetate as carbon source; the growth yield under these conditions was 1.4g of cell protein per mol chloride released. Alternatively to PCE, fumarate and nitrate could serve as electron acceptors; sulfate could not replace fumarate, nitrate, or PCE in this respect. In addition to H2, the organism utilized a variety of electron donors for dechlorination (pyruvate, lactate, ethanol, formate, glycerol). Upon growth on pyruvate plus PCE, the main fermentation products formed were acetatc, lactate, DCE, and H2. At optimal pH (7.3–7.6) and temperature (30°C), and in the presence of pyruvate (20mM) and PCE (160μM), a dechlorination rate of about 50 nmol min-1 (mg cell protein)-1 and a doubling time of about 2.5h were obtained with growing cultures. The ability to reduce PCE to DCE appears to be constitutive under the experimental conditions applied since cultures growing in the absence of PCE for several generations immediately started dechlorination when transferred to a medium containing PCE. The organism may be useful for bioremediation of environments polluted with tetrachloroethene.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Archives of microbiology 163 (1995), S. 276-281 
    ISSN: 1432-072X
    Keywords: Tetrachloroethene ; Trichloroethene ; Dichloroethene ; PCE dehalogenase ; TCE dehalogenase ; Corrinoid ; Vitamin B12 ; Dehalospirillum multivorans ; Reductive dechlorination ; Tetrachloroethene respiration
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Some properties of tetrachloroethene and trichloroethene dehalogenase of the recently isolated, tetrachloroethene-utilizing anaerobe, Dehalospirillum multivorans, were studied with extracts of cells grown on pyruvate plus fumarate. The dehalogenase catalyzed the oxidation of reduced methyl viologen with tetrachloroethene (PCE) or trichloroethene (TCE) as electron acceptor. All other artificial or physiological electron donors tested were ineffective. The PCE and TCE dehalogenase activity was insensitive towards oxygen in crude extracts. When extracts were incubated under anoxic conditions in the presence of titanium citrate as reducing agent, the dehalogenase was rapidly inactivated by propyl iodide (50 μM). Inactivation did not occur in the absence of titanium citrate. The activity of propyl-iodide-treated extracts was restored almost immediately by illumination. The dehalogenase was inhibited by cyanide. The inhibition profile was almost the same under oxic and anoxic conditions independent of the presence or absence of titanium citrate. In addition, N2O, nitrite, and ethylene diamine tetra-acetate (EDTA) were inhibitors of PCE and TCE dehalogenase. Carbon monoxide and azide had no influence on the dehalogenase activity. Trans-1,2-dichloroethene or 1,1-dichloroethene, both of which are isomers of the dechlorination product cis-1,2-dichloroethene, neither inhibited nor inactivated the dehalogenase. PCE and TCE dechlorination appeared to be mediated by the same enzyme since the inhibitors tested had nearly the same effects on the PCE and TCE dehalogenating activity. The data indicated the involvement of a corrinoid and possibly of an additional transition metal in reductive PCE and TCE dechlorination.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1432-072X
    Keywords: Methylenetetrahydrofolate ; Methyltetrahydrofolate ; Methylenetetrahydrofolate reductase ; Homoacetogenic bacteria ; Energy conservation of homoacetogens
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The thermodynamics of the methylenetetrahydrofolate reduction to 5-methyltetrahydrofolate was studied with the methylenetetrahydrofolate reductase purified from the homoacetogenic bacterium Peptostreptococcus productus. The equilibrium constants were determined for the forward and backward reactions of methylenetetrahydrofolate reduction with NADH or acetylpyridine adenine dinucleotide (APADH), respectively, as the electron donors. From the equilibrium constants and the known standard redox potentials at pH 7 (E o′ ) of the couples NAD+/NADH or APAD+/APADH the E o′ of the couple methylene-/methyltetrahydrofolate was determined to be about-200mV. This value is different from values reported before for this couple. The implications for the mechanism of energy conservation of homoacetogens is discussed.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Archives of microbiology 160 (1993), S. 383-387 
    ISSN: 1432-072X
    Keywords: Homoacetogenic bacteria ; Acetate formation from methyl chloride ; Strain MC ; Tetrahydrofolate enzymes ; Methyl tetrahydrofolate foramtion ; Anaerobic dechlorination ; O-demethylation of methoxylated aromatics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The methyl chloride metabolism of the homoacetogenic, methyl chloride-utilizing strain MC was investigated with cell extracts and cell suspensions of the organism. Cell extracts were found to contain all enzyme activities required for the conversion of methyl chloride or of H2 plus CO2 to acetate. They catalyzed the dechlorination of methyl chloride with tetrahydrofolate as the methyl acceptor at a rate of ∼20 nmol/min × mg of cell protein. Also, the O-demethylation of vanillate with tetrahydrofolate could be measured at a rate of 40 nmol/min × mg. Different enzyme systems appeared to be responsible for the dehalogenation of CH3Cl and for the O-demethylation of methoxylated aromatic compounds, since cells grown with methoxylated aromatic compounds exhibited a significantly lower activity of CH3Cl conversion than methyl chloride grown cells and vice versa. In addition, ammonium thiocyanate (5 mM) completely inhibited CH3Cl dechlorination, whereas the consumption of vanillate was not affected significantly. The data were taken to indicate, that the methyl chloride dehalogenation is catalyzed by a specific, inducible enzyme present in strain MC, and that tetrahydrofolate rather than the corrinoid-protein involved in acetate formation is the primary acceptor of the methyl group in the dechlorination reaction.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Archives of microbiology 122 (1979), S. 117-120 
    ISSN: 1432-072X
    Keywords: Nickel ; Carbon monoxide oxidation ; Clostridium pasteurianum ; Nitrilotriacetate
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Formation of carbon monoxide dehydrogenase in growing Clostridium pasteurianum was found to be dependent on trace nickel present as contaminant in the growth medium. The evidence is: i) Synthesis of the enzyme was increased, when NiCl2 (0.1 μM) was added to the medium; ii) Synthesis of the enzyme was almost completely inhibited when the cells were grown in the presence of nitrilotriacetate (0.1 mM) or of other chelating agents, which inhibited the uptake of trace nickel from the medium; iii) Inhibition of enzyme synthesis by the chelators could be specifically overcome by supplementing the medium with nickel (1μM).
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Archives of microbiology 156 (1991), S. 416-421 
    ISSN: 1432-072X
    Keywords: Methyl chloride utilization ; Homoacetogenic bacteria ; Anaerobic dehalogenation ; Strain MC ; Methylotrophic anaerobes ; Methoxylated aromatic compounds
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract From sludge obtained from the sewage digester plant in Stuttgart-Möhringen a strictly anaerobic bacterium was enriched and isolated with methyl chloride as the energy source. The isolate, which was tentatively called strain MC, was nonmotile, gram-positive, and occurred as elongated cocci arranged in chains. Cells of strain MC formed about 3 mol of acetate per 4 mol of CH3Cl consumed, indicating that the organism was a homoacetogenic bacterium fermenting methyl chloride plus CO2 according to: $$\begin{gathered} 4 CH_3 Cl + 2 CO_2 + 2 H_2 O \to 3 CH_3 COO^ - \hfill \\ + 7 H^ + + 4 Cl^ - . \hfill \\ \end{gathered} $$ The organism grew with 2–3% methyl chloride in the gas phase at a doubling time of near 30 h. Dichloromethane was not utilized. The bacterium also grew on carbon monoxide, H2 plus CO2, and methoxylated aromatic compounds. Optimal growth with methyl chloride was observed at 25°C and pH 7.3–7.7. The G+C-content of the DNA was 47.5±1.5%. The methyl chloride conversion appeared to be inducible, since H2 plus CO2-grown cells lacked this ability. From the morphological and physiological characteristics, the isolate could not be affiliated to a known species.
    Type of Medium: Electronic Resource
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