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Talaam, K. Hartuti, E. Matsuo, Y. Sakura, T. Gloria, B. Hidano, S. Kido, Y. Mori, M. Shiomi, K. Sekijima, M. Nozaki, T. Umeda, K. Nishikawa, Y. Hamano, S. Kita, K. Inaoka, D. Acharjee, R. Need Help? Support Find support for a specific problem in the support section of our website. Get Support. Feedback Please let us know what you think of our products and services. Give Feedback. Get Information.

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Open Access Article. Keith K. Endah D. Yuichi Matsuo. Takaya Sakura. Bundutidi M. Shinya Hidano. Yasutoshi Kido.

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Mihoko Mori. Kazuro Shiomi. Masakazu Sekijima. Tomoyoshi Nozaki. Kousuke Umeda.

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Yoshifumi Nishikawa. Shinjiro Hamano. Kiyoshi Kita. Daniel K. BoxCongo. Author to whom correspondence should be addressed. The red arrows show visible bands by both GelCode Blue and activity stainings, corresponding to tetramer and dimer of tetramer of TgMQO, respectively.

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The blue and yellow dots represent the molecular weights of tetramer kDa and dimer of tetramer kDa of TgMQO, respectively. In each case, the reaction was initiated with 10 mM malate.

Behavior of polymer materials exposed to aging in the swimming pool: focus on properties that assure comfort and durability

The resulting lines intersecting above the X-axis in the second quadrant indicate a sequential mechanism of the reaction. In both cases, the double reciprocal lines intersected in the second quadrant, indicating a mixed type inhibition of TgMQO activity. Toxoplasma gondii is a protozoan parasite that causes toxoplasmosis and infects almost one-third of the global human population.

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A lack of effective drugs and vaccines and the emergence of drug resistant parasites highlight the need for the development of new drugs. The mitochondrial electron transport chain ETC is an essential pathway for energy metabolism and the survival of T. In apicomplexan parasites, malate:quinone oxidoreductase MQO is a monotopic membrane protein belonging to the ETC and a key member of the tricarboxylic acid cycle, and has recently been suggested to play a role in the fumarate cycle, which is required for the cytosolic purine salvage pathway.

This system allowed, for the first time, the expression and purification of a mitochondrial MQO family enzyme, which was used for steady-state kinetics and substrate specificity analyses.

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Furthermore, our analysis indicated the presence of a third binding site for ferulenol that is distinct from the ubiquinone and malate sites. Keywords: toxoplasmosis; electron transport chain; mitochondria; membrane protein; enzyme inhibition; ferulenol toxoplasmosis ; electron transport chain ; mitochondria ; membrane protein ; enzyme inhibition ; ferulenol.

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Introduction Toxoplasmosis is a zoonosis caused by Toxoplasma gondiian obligate intracellular apicomplexan protozoan parasite that can infect almost all nucleated cells [ 1234 ]. It has long been considered a mild pathogen compared to other deadly apicomplexan novel games pool such as Plasmodium falciparum [ 6 ], the pathogen of malaria, though in many aspects T. The capacity of T. A correlation between the geographical variations of T. Among three known and well-characterized lineages of T. The seroprevalence is high [ 15 ], perhaps due to ease of transmission of T. Typically, the disease is asymptomatic in immunocompetent hosts, but provokes severe illness in immunocompromised patients such as those with acquired immunodeficiency syndrome, pregnant women, or congenitally infected individuals [ 1617 ]; without treatment, it can lead to death [ 18 ].

To date, toxoplasmosis chemotherapy options are limited, and all drugs currently used have severe side effects, are solely active against tachyzoites, and not able to clear cystic chronic infection [ 1920 ]. Furthermore, Toxovax, the only vaccine for animal toxoplasmosis, is not suitable for humans because of iatrogenic infection risks and interconversion of parasite stages [ 2122 ].

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Therefore, it is needed to develop new drugs for both tachyzoites and bradyzoites in cysts with novel mechanisms of action with fewer side effects [ 19 ]. Undoubtedly, metabolic pathways or molecular targets from the parasites that are absent or different from the corresponding host pathways are attractive drug targets [ 1923 ]. Although glucose and glutamine are the major carbon sources, the metabolic plasticity of T. However, to support the optimal growth of T.

studies have revealed the presence of a functional tricarboxylic acid TCA cycle in tachyzoites [ 2427 ]. Moreover, the comparative expression analysis of TCA cycle enzymes has shown similar mRNA levels between tachyzoites and early bradyzoites [ 27 ].

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Collectively, these findings suggest that, to meet its energy demands, this parasite acquires adenosine triphosphate ATP not only by glycolysis but also by oxidative phosphorylation.