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metabolism
the electrons released from pyrroloquinoline quinone during the oxidation successively reduce cytochrome cL, cytochrome cH and finally the membrane oxidase cytochrome aa3. As a result of the oxidoreduction pathway, a proton electrochemical gradient is produced around the membrane, which in turn drives the generation of one ATP molecule per molecule of methanol
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the enzyme contains the prosthetic group pyrroloquinoline quinone, PQQ, which catalyzes the oxidation of methanol to formaldehyde, active site structure with pyrroloquinoline quinone and Ca2+, substrate binding structure, overview
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type II MDH has higher specific activity than type I MDH. The original conformation of the MDH Methylophaga aminisulfidivorans MPT is most likely the alpha2beta2-MxaJ complex. The lysozyme and freeze-thawing cell disruption method significantly increases the amount of type II MDH in the soluble fraction compared with strong physical disruption methods such as sonication and French Press; type II MDH has higher specific activity than type I MDH. The original conformation of the MDH Methylophaga aminisulfidivorans MPT is most likely the alpha2beta2-MxaJ complex. The lysozyme and freeze-thawing cell disruption method significantly increases the amount of type II MDH in the soluble fraction compared with strong physical disruption methods such as sonication and French Press
Results 1 - 3 of 3