Clint Kisting

Clint Kisting

Greater St. Louis
569 followers 500+ connections

About

Experienced Area Sales Manager with a demonstrated history of working in the industrial…

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Experience

  • Cytiva Graphic

    Cytiva

    Greater St. Louis

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    Greater St. Louis

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Education

Publications

  • Growth of Rhodospirillum rubrum on synthesis gas: conversion of CO to H2 and poly-beta-hydroxyalkanoate.

    Biotechnology and Bioengineering

    To examine the potential use of synthesis gas as a carbon and energy source in fermentation processes, Rhodospirillum rubrum was cultured on synthesis gas generated from discarded seed corn. The growth rates, growth and poly-β-hydroxyalkanoates (PHA) yields, and CO oxidation/H2 evolution rates were evaluated in comparison to the rates observed with an artificial synthesis gas mixture. Depending on the gas conditioning system used, synthesis gas either stimulated or inhibited CO-oxidation rates…

    To examine the potential use of synthesis gas as a carbon and energy source in fermentation processes, Rhodospirillum rubrum was cultured on synthesis gas generated from discarded seed corn. The growth rates, growth and poly-β-hydroxyalkanoates (PHA) yields, and CO oxidation/H2 evolution rates were evaluated in comparison to the rates observed with an artificial synthesis gas mixture. Depending on the gas conditioning system used, synthesis gas either stimulated or inhibited CO-oxidation rates compared to the observations with the artificial synthesis gas mixture. Inhibitory and stimulatory compounds in synthesis gas could be removed by the addition of activated charcoal, char-tar, or char-ash filters (char, tar, and ash are gasification residues). In batch fermentations, approximately 1.4 mol CO was oxidized per day per g cell protein with the production of 0.75 mol H2 and 340 mg PHA per day per g cell protein. The PHA produced from R. rubrum grown on synthesis gas was composed of 86% β-hydroxybutyrate and 14% β-hydroxyvalerate. Mass transfer of CO into the liquid phase was determined as the rate-limiting step in the fermentation

  • Spectral, kinetic, and thermodynamic properties of Cu(I) and Cu(II) binding by methanobactin from Methylosinus trichosporium OB3b.

    Biochemistry

    To examine the potential role of methanobactin (mb) as the extracellular component of a
    copper acquisition system in Methylosinus trichosporium OB3b, the metal binding properties of mb were
    examined. Spectral (UV-visible, fluorescence, and circular dichroism), kinetic, and thermodynamic data
    suggested copper coordination changes at different Cu(II):mb ratios. Mb appeared to initially bind Cu(II)
    as a homodimer with a comparatively high copper affinity at Cu(II):mb ratios below 0.2…

    To examine the potential role of methanobactin (mb) as the extracellular component of a
    copper acquisition system in Methylosinus trichosporium OB3b, the metal binding properties of mb were
    examined. Spectral (UV-visible, fluorescence, and circular dichroism), kinetic, and thermodynamic data
    suggested copper coordination changes at different Cu(II):mb ratios. Mb appeared to initially bind Cu(II)
    as a homodimer with a comparatively high copper affinity at Cu(II):mb ratios below 0.2, with a binding
    constant (K) greater than that of EDTA (log K ) 18.8) and an approximate !G° of -47 kcal/mol. At
    Cu(II):mb ratios between 0.2 and 0.45, the K dropped to (2.6 ( 0.46) × 108 with a !G° of -11.46
    kcal/mol followed by another K of (1.40 ( 0.21) × 106 and a !G° of -8.38 kcal/mol at Cu(II):mb ratios
    of 0.45-0.85. The kinetic and spectral changes also suggested Cu(II) was initially coordinated to the
    4-thiocarbonyl-5-hydroxy imidazolate (THI) and possibly Tyr, followed by reduction to Cu(I), and then
    coordination of Cu(I) to 4-hydroxy-5-thiocarbonyl imidazolate (HTI) resulting in the final coordination
    of Cu(I) by THI and HTI. The rate constant (kobsI) of binding of Cu(II) to THI exceeded that of the
    stopped flow apparatus that was used, i.e., >640 s-1, whereas the coordination of copper to HTI showed
    a 6-8 ms lag time followed by a kobsII of 121 ( 9 s-1. Mb also solubilized and bound Cu(I) with a kobsI
    to THI of >640 s-1, but with a slower rate constant to HTI (kobsII ) 8.27 ( 0.16 s-1), and appeared to
    initially bind Cu(I) as a monomer.

Languages

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