Biochemical characterization of archaeal homocitrate synthase from Sulfolobus acidocaldarius

The hyperthermophilic archaeon, Sulfolobus, synthesizes lysine via the α‐aminoadipate pathway; however, the gene encoding homocitrate synthase, the enzyme responsible for the first and committed step of the pathway, has not yet been identified. In the present study, we identified saci_1304 as the ge...

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Veröffentlicht in:FEBS letters 2020-01, Vol.594 (1), p.126-134
Hauptverfasser: Suzuki, Tomohiro, Akiyama, Nagisa, Yoshida, Ayako, Tomita, Takeo, Lassak, Kerstin, Haurat, Maria Florencia, Okada, Takuya, Takahashi, Kento, Albers, Sonja‐Verena, Kuzuyama, Tomohisa, Nishiyama, Makoto
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Sprache:eng
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Zusammenfassung:The hyperthermophilic archaeon, Sulfolobus, synthesizes lysine via the α‐aminoadipate pathway; however, the gene encoding homocitrate synthase, the enzyme responsible for the first and committed step of the pathway, has not yet been identified. In the present study, we identified saci_1304 as the gene encoding a novel type of homocitrate synthase fused with a Regulation of Amino acid Metabolism (RAM) domain at the C terminus in Sulfolobus acidocaldarius. Enzymatic characterization revealed that Sulfolobus homocitrate synthase was inhibited by lysine; however, the mutant enzyme lacking the RAM domain was insensitive to inhibition by lysine. The present results indicated that the RAM domain is responsible for enzyme inhibition.
ISSN:0014-5793
1873-3468
DOI:10.1002/1873-3468.13550