The major source of NADH in R erythropolis is the carbon metabol

The major source of NADH in R. erythropolis is the carbon metabolism. Ethanol yields more NADH during this metabolism than glucose and glycerol. The additional NADH enables the cell to increase the flux (or desulfurizing rate) of the 4S pathway, which eventually helps it to increase growth. Extending this, we argue that a carbon source that provides more NADH

is likely to enhance both the growth and the desulfurizing rates of R. erythropolis. As our model predicted some experimental observations successfully, we examined the suitability of additional carbon sources for desulfurizing activity. We studied citrate, ethanol, fructose, gluconate, glucose, glycerol, glutamate, and lactate as possible sole carbon sources. We computed fluxes for each sole source separately with an Erlotinib concentration uptake rate of 20 mg g−1 dcw h−1.

Figure 4 shows the results of our eight simulation runs. The desulfurization and growth rates relative to those of ethanol decrease in the following order: ethanol (0.18 mmol HBP g−1 dcw h−1 as 100% and 1.39 h−1 as 100%)>lactate (67%)>citrate (48%)>glutamate (44%)>glucose=fructose (43%)>glycerol (42%)>gluconate (40%). However, as our model is reduced and has limited scope, this prediction is only qualitative in nature. An experimental verification of this prediction is clearly beyond the scope of this work. As a natural goal of any MK0683 in silico model, our intention is simply to offer a new hypothesis that experimental researchers can verify. Our reconstructed stoichiometric model for sulfur metabolism in R. erythropolis successfully predicted cell growth and several known/unknown phenotypes. Our analysis shows that NADH plays a critical role in desulfurization activity. Any changes in medium design or genetic manipulations that increase NADH regeneration and supply within the cellular metabolism are likely to enhance desulfurization activity. We are in the process of developing a full genome-scale model that can account for host functions other than just sulfur and central 2-hydroxyphytanoyl-CoA lyase metabolism. Table S1. Metabolite and reaction content of the model. Please note: Wiley-Blackwell is not responsible for the

content or functionality of any supporting materials supplied by the authors. Any queries (other than missing material) should be directed to the corresponding author for the article. “
“Fusarium species can produce mycotoxins, which can contaminate cereal-based food producing adverse effects for human and animal health. In recent years, the importance of Fusarium poae has increased within the Fusarium head blight complex. Fusarium poae is known to produce trichothecenes, especially nivalenol, a potent mycotoxin able to cause a variety of toxic effects. In this study, a specific primer pair was designed based on the tri7 gene to detect potential nivalenol-producing F. poae isolates. A total of 125 F. poae, four F. cerealis, two F. culmorum, one F. langsethiae, one F. sporotrichioides and seven F.

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