We measured the uptake rate of molybdatc and related kinetic parameters for nine taxa of cyanobacteria and for the natural phytoplankton communities of six freshwater lakes containing planktonic Nz-fixing cyanobacteria. Molybdate uptake followed saturation kinetics and was competitively inhibited by both tungstate and sulfate. Tungstate inhibited molybdate uptake in a nearly mole-for-mole fashi...

When Escherichia coli was grown in the presence of tungstate, inactive forms of two molybdoenzymes, nitrate reductase and formate dehydrogenase, accumulated and were converted to their active forms upon incubation of cell suspensions with molybdate and chloramphenicol. The conversion to the active enzymes did not occur in cell extracts. When incubated with [(99)Mo]molybdate and chloramphenicol,...

Clearly there are differences in the observed reactivities of the "heavily oxidized" surfaces of Mo(1 I0) prepared by Queeney et al. [1] and those prepared by us [2]. We note, however, that our study is in agreement with, and provides fresh insight into, the chemistry of high surface-area (HSA), "real-world" molybdate catalysts. The 3D oxide prepared by us (i) does not produce methyl radicals, ...

1. [35S]sulphate was used to measure the apparent turnover of sulphate, sulphide and microbial-protein-S in the rumen contents of four sheep that were intraruminally infused with 10 g sodium sulphate/d alone, or together with 126 mg sodium molybdate (50 mg molybdenum). 2. Infusion of molybdate increased the concentration of sulphate in rumen fluid from 2.2 to 7.2 mug S/ml and decreased the rate...

Anabaena variabilis fixes nitrogen under aerobic growth conditions in differentiated cells called heterocysts using either a Mo nitrogenase or a V nitrogenase. The nifH1 gene, which encodes the dinitrogenase reductase of the Mo nitrogenase that is expressed only in heterocysts, is cotranscribed with nifD1 and nifK1, which together encode the Mo dinitrogenase. These genes were expressed in the p...

The reaction of Na2MoO4 with 2,2'-oxydianiline (2-aminophenylether), (2-NH2C6H4)2O, LH4, in DME (DME = 1,2-dimethoxyethane) in the presence of Et3N and Me3SiCl afforded either the bis(imido) molybdenum(vi) complex {Mo(L)Cl2(DME)} (), where L = (2-NC6H4)2O, or the molybdenum(v) salt [Mo(L')Cl4][Et3NH] (), where L' = [(2-NH2C6H4)(2-NC6H4)O], depending on the work-up method employed. The same diam...

The title compound, tris-(4,4'-bipyridinium) diarsenoocta-deca-molybdate(VI), (C(10)H(10)N(2))(3)[As(2)Mo(18)O(62)], featuring protonated bipyridine mol-ecules and a classical Dawson-type polyoxo-anion, has been synthesized under hydro-thermal conditions. The polyoxoanions are linked together via the bipyridyl cations, acting as hydrogen-bond donors, generating a two-dimensional supra-molecular...

Nickel molybdate (NiMoO₄) nanoparticles were synthesized via calcination of an oxalate complex in static air at 500 °C. The oxalate complex was analyzed by thermal gravimetric analysis (TGA) and Fourier transform infrared spectroscopy (FTIR). The as-synthesized nickel molybdate was characterized by Brunauer-Emmett-Teller technique (BET), X-ray diffraction (XRD), and transmission electron micros...

Thiobacillus novellus shows a maximum induction of sulfite oxidase activity and a maximum growth rate as a result of supplementing the autotrophic growth medium with 4.0 microM ammonium molybdate. Cells grown in the presence of molybdate showed approximately 10-fold increases in the amount of enzyme-associated molybdenum and in the sulfite-to-cytochrome c and sulfite-to-ferricyanide reductase a...