PubMed · 12506926
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2002. Space colonization.. https://pubmed.ncbi.nlm.nih.gov/12506926/
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Analytical expressions were derived for calculating the sensitivities of isotopomer distribution vectors, the weighted output matrix with respect to the fluxes, and the covariance matrix for the metabolic flux analysis based on isotopomers mapping matrices (IMM). These expressions allow us to implement efficient statistical analysis, avoiding the time-consuming Monte Carlo techniques for estimating the confidence interval of the fluxes. The analytical expressions are also useful in implementing a faster design of experiment, which requires repetitive computation of the covariance matrix that is not straightforward to make in practice with the numerical techniques based on the conventional IMM. The proposed method was applied for analyzing the central carbon metabolism of the mixotrophically cultivated Synechocystis sp. PCC6803, and the confidence intervals of all its fluxes were computed based on the isotopomer distribution measured using NMR and GC-MS. It was found that the best feasible mixture for labeling experiment is 70% unlabeled, 10% [U-13C] and 20% [1,2-13C2] labeled glucose to obtain the most reliable metabolic fluxes.
Local photosynthetic photon flux fluence rate (PPFFR) determined by a submersible 4pi quantum micro-sensor was used in developing a versatile on-line state estimator for stirred-tank microalgal photobioreactor cultures. A marine micro-alga Dunaliella salina was used as a model organism in this study. On-line state estimation was realized using the extended Kalman filter (EKF), based on a state model of the photobioreactor and on-line local PPFFR measurement. The dynamic state model for the photobioreactor was derived based on mass-balance equations of the relevant states. The measurement equation was established based on an empirical correlation between the microalgal biomass concentration and the local PPFFR measured at a fixed point inside the photobioreactor. An internal model approach was used to estimate the specific growth rate without the need of state-based kinetic expression. The estimator was proven to be capable of estimating biomass concentration and specific growth rate, as well as phosphate and dissolved oxygen concentrations in a photobioreactor illuminated with either fixed or time-varying incident radiation. The quantum sensor was shown to be robust and able to quickly respond to dynamic changes in local PPFFR. In addition, the quantum sensor outputs were not affected by bubble aeration or agitation within the typical operating range. The strong filtering capacity of EKF gives the state estimator superior performance compared to direct calculation from the empirical biomass/local PPFFR correlation. This state estimation system makes use of inexpensive and reliable sensor hardware to report key process dynamics of microalgal photobioreactor cultures on-line, enabling improved operation of such a process.
In order to develop a method for use in investigations of spatial biomass distribution in solid-state fermentation systems, confocal scanning laser microscopy was used to determine the concentrations of aerial and penetrative biomass against height and depth above and below the substrate surface, during growth of Rhizopus oligosporus on potato dextrose agar. Penetrative hyphae had penetrated to a depth of 0.445 cm by 64 h and showed rhizoid morphology, in which the maximum biomass concentration, of 4.45 mg dry wt cm(-3), occurred at a depth of 0.075 cm. For aerial biomass the maximum density of 39.54 mg dry wt (-3) occurred at the substrate surface. For both aerial and penetrative biomass, there were two distinct regions in which the biomass concentration decayed exponentially with distance from the surface. For aerial biomass, the first exponential decay region was up to 0.1 cm height. The second region above the height of 0.1 cm corresponded to that in which sporangiophores dominated. This work lays the foundation for deeper studies into what controls the growth of fungal hyphae above and below the surfaces of solid substrates.