Publication: Catalytic and structural insights into a stereospecific and thermostable class II aldolase HpaI from Acinetobacter baumannii
Issued Date
2021-11-01
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ISSN
1083351X
00219258
00219258
Other identifier(s)
2-s2.0-85118931040
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Mahidol University
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SCOPUS
Bibliographic Citation
Journal of Biological Chemistry. Vol.297, No.5 (2021)
Suggested Citation
Pratchaya Watthaisong, Asweena Binlaeh, Aritsara Jaruwat, Narin Lawan, Jirawat Tantipisit, Juthamas Jaroensuk, Litavadee Chuaboon, Jittima Phonbuppha, Ruchanok Tinikul, Pimchai Chaiyen, Penchit Chitnumsub, Somchart Maenpuen Catalytic and structural insights into a stereospecific and thermostable class II aldolase HpaI from Acinetobacter baumannii. Journal of Biological Chemistry. Vol.297, No.5 (2021). doi:10.1016/j.jbc.2021.101280 Retrieved from: https://repository.li.mahidol.ac.th/handle/20.500.14594/75973
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Title
Catalytic and structural insights into a stereospecific and thermostable class II aldolase HpaI from Acinetobacter baumannii
Abstract
Aldolases catalyze the reversible reactions of aldol condensation and cleavage and have strong potential for the synthesis of chiral compounds, widely used in pharmaceuticals. Here, we investigated a new Class II metal aldolase from the p-hydroxyphenylacetate degradation pathway in Acinetobacter baumannii, 4-hydroxy-2-keto-heptane-1,7-dioate aldolase (AbHpaI), which has various properties suitable for biocatalysis, including stereoselectivity/stereospecificity, broad aldehyde utilization, thermostability, and solvent tolerance. Notably, the use of Zn2+ by AbHpaI as a native cofactor is distinct from other enzymes in this class. AbHpaI can also use other metal ion (M2+) cofactors, except Ca2+, for catalysis. We found that Zn2+ yielded the highest enzyme complex thermostability (Tm of 87 °C) and solvent tolerance. All AbHpaI·M2+ complexes demonstrated preferential cleavage of (4R)-2-keto-3-deoxy-D-galactonate ((4R)-KDGal) over (4S)-2-keto-3-deoxy-D-gluconate ((4S)-KDGlu), with AbHpaI·Zn2+ displaying the highest R/S stereoselectivity ratio (sixfold higher than other M2+ cofactors). For the aldol condensation reaction, AbHpaI·M2+ only specifically forms (4R)-KDGal and not (4S)-KDGlu and preferentially catalyzes condensation rather than cleavage by ~40-fold. Based on 11 X-ray structures of AbHpaI complexed with M2+ and ligands at 1.85 to 2.0 Å resolution, the data clearly indicate that the M2+ cofactors form an octahedral geometry with Glu151 and Asp177, pyruvate, and water molecules. Moreover, Arg72 in the Zn2+-bound form governs the stereoselectivity/stereospecificity of AbHpaI. X-ray structures also show that Ca2+ binds at the trimer interface via interaction with Asp51. Hence, we conclude that AbHpaI·Zn2+ is distinctive from its homologues in substrate stereospecificity, preference for aldol formation over cleavage, and protein robustness, and is attractive for biocatalytic applications.