Título:	Functional genomics and structural insights into maize aldo-keto reductase-4 family: Stress metabolism and substrate specificity in embryos.
Autoria:	SOUSA, S. M. de GIUSEPPE, P. O. de MURAKAMI, M. T. GUAN, J.-C. SAUNDERS, J. W. KIYOTA, E. SANTOS, M. L. SCHMELZ, E. A. YUNES, J. A. KOCH, K. E.
Afiliação:	SYLVIA MORAIS DE SOUSA TINOCO, CNPMS; PRISCILA OLIVEIRA DE GIUSEPPE, CENTRO BRASILEIRO DE PESQUISA EM ENERGIA E MATERIAIS; MARIO TYAGO MURAKAMI, CENTRO BRASILEIRO DE PESQUISA EM ENERGIA E MATERIAIS; JIAHN-CHOU GUAN, UNIVERSITY OF FLORIDA; JONATHAN W. SAUNDERS, UNIVERSITY OF FLORIDA; EDUARDO KIYOTA, UNIVERSIDADE ESTADUAL DE CAMPINAS; MARCELO LEITE SANTOS, UNIVERSIDADE ESTADUAL DE CAMPINAS; ERIC A. SCHMELZ, UNIVERSITY OF CALIFORNIA; JOSE ANDRES YUNES, CENTRO INFANTIL BOLDRINI; KAREN E. KOCH, UNIVERSITY OF FLORIDA.
Ano de publicação:	2025
Referência:	Journal of Biological Chemistry, v. 301, n. 7, 110404, 2025.
Conteúdo:	Aldo-keto reductases (AKRs) are ubiquitous in nature and are able to reduce a wide range of substrates, from simple sugars to potentially toxic aldehydes. In plants, AKRs are involved in key metabolic processes including reactive aldehyde detoxification. This study aimed to (i) delineate a maize gene family encoding aldo keto reductase-4s (AKR4s) (ii) help bridge sequence-tofunction gaps among them, and (iii) focus on a family member implicated in embryo specific stress metabolism. We employed a genome-wide analysis approach to identify maize genes encoding AKR4s, defining and annotating a 15-member gene family that clustered into three subgroups. Expression profiling, validated through wet lab experiments, revealed distinct functional roles: (i) AKR4C Zm-1 functions in aldehyde detoxification during stress, (ii) AKR4C Zm-2 includes stress-responsive AKRs with diverse substrate affinities, and (iii) AKR4A/B Zm-3 contributes to specialized metabolites like phytosiderophores for iron transport. To investigate the impact of sequence variation on function, we characterized ZmAKR4C13, a representative of AKR4C Zm-1. Its mRNA and protein were predominantly localized in embryos, suggesting a specialized role. Recombinant ZmAKR4C13 efficiently reduced methylglyoxal and small aldehydes but showed poor activity toward aldoses larger than four carbons. Crystallographic analysis identified a size constraint at the active site, attributed to the bulkier LEU residue at position 294. Collectively, our results emphasize how subtle modifications in active-site architecture influence AKR substrate specificity. They also demonstrate a potential role of maize ZmAKR4C13 in detoxifying methylglyoxal and other small metabolites that could contribute to stress signaling in embryos.
Thesagro:	Milho Gene Enzima
Palavras-chave:	Aldo-ceto redutase Análise genômica
Digital Object Identifier:	https://doi.org/10.1016/j.jbc.2025.110404
Tipo do material:	Artigo de periódico
Acesso:	openAccess
Aparece nas coleções:	Artigo em periódico indexado (CNPMS)