The rapid and reliable diagnosis of anaerobic bacteria constitutes one of the key procedures in clinical microbiology. Automatic jar gassing systems are commonly used laboratory instruments for this purpose. The most critical factors affecting the cultivation performance of these systems are the level of residual oxygen remaining in the anaerobic jar and the reaction rate determined by the Pd/AlO catalyst. The main objective of the presented study is to design and manufacture an enhanced jar gassing system equipped with an extremum seeking-based estimation algorithm that combines real-time data and a reaction model of the Pd/AlO catalyst. The microkinetic behavior of the palladium catalyst was modeled through a learning-from-experiment methodology. The majority of microkinetic model parameters were derived from material characterization analysis. A comparative validation test of the designed cultivation system was conducted using conventional gas pouches via six different bacterial strains. The results demonstrated high cell viability, with colony counts ranging from 1.26 × 10 to 2.17 × 10 CFU mL. The favorable catalyst facets for water formation on Pd surfaces and the crystal structure of Pd/AlO pellets were identified by X-Ray diffraction analysis (XRD). The doping ratio of the noble metal (Pd) and the support material (AlO) was validated via energy-dispersive spectroscopy (EDS) measurements as 0.68% and 99.32%, respectively. The porous structure of the catalyst was also analyzed by scanning electron microscopy (SEM). During the reference clinical trial, the estimation algorithm was terminated after 878 iterations, having reached its predetermined termination value. The measured and modelled reaction rates were found to converge with a root-mean-squared error (RMSE) of less than 10, and the Arrhenius parameters of ongoing catalytic reaction were obtained. Additionally, our research offers a comprehensive analysis of anaerobic jar gassing systems from an engineering perspective, providing novel insights that are absent from the existing literature.
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http://dx.doi.org/10.3390/bioengineering11111068 | DOI Listing |
Bioengineering (Basel)
October 2024
Institute of Health Sciences, Marmara University, 34865 Istanbul, Turkey.
Isolation of Campylobacter spp. using enrichment culture is time consuming and complex. Reducing the time taken to confirm the presence or absence of Campylobacter spp.
View Article and Find Full Text PDFBull Soc Pathol Exot
February 2007
Centre de recherche et de formation sur le paludisme, Département d'épidemiologie des affections parasitaires, Faculté de medecine, de pharmacie et d'odonto-stomatologie, Université de Bamako, Mali.
Malaria immunology, molecular biology and pathogenicity studies often require the adaptation of Plasmodium falciparum field isolates to continuous in vitro cultivation. For this purpose we have established propagation protocols of asexual erythrocytic stages of P. falciparum samples from malaria patients or asymptomatic carriers in Mali.
View Article and Find Full Text PDFJ Clin Microbiol
November 1987
Anti-Infective Research Department, Norwich Eaton Pharmaceuticals, Inc., New York 13815.
Until recently, broth cultivation techniques for Campylobacter pylori were unavailable. We developed a method to cultivate bacterial cells within 24 h in liquid media. Cultivation in broth depended on the adequate dispersion of appropriate gases.
View Article and Find Full Text PDFJ Clin Microbiol
December 1982
We determined the effect of performing antimicrobial susceptibility tests in five different anaerobic incubation systems: GasPak jar, large GasPak jar, evacuated-gassed anaerobic jar, anaerobic chamber, and Bio-Bag. Growth of the anaerobes was equivalent in all five incubation systems. The results of testing 38 anaerobes against 11 antimicrobial agents were comparable for the anaerobic jars and anaerobic chamber.
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