The d -2-Hydroxyacid Dehydrogenase Incorrectly Annotated PanE Is the Sole Reduction System for Branched-Chain 2-Keto Acids in Lactococcus lactis

Author:

Chambellon Emilie1,Rijnen Liesbeth2,Lorquet Frédérique1,Gitton Christophe1,van Hylckama Vlieg Johan E. T.2,Wouters Jeroen A.2,Yvon Mireille1

Affiliation:

1. INRA, UR 477 Biochimie Bactérienne, F-78350 Jouy-en-Josas, France

2. Department of Flavour, NIZO Food Research B.V., 6710 BA Ede, The Netherlands

Abstract

ABSTRACT Hydroxyacid dehydrogenases of lactic acid bacteria, which catalyze the stereospecific reduction of branched-chain 2-keto acids to 2-hydroxyacids, are of interest in a variety of fields, including cheese flavor formation via amino acid catabolism. In this study, we used both targeted and random mutagenesis to identify the genes responsible for the reduction of 2-keto acids derived from amino acids in Lactococcus lactis . The gene panE , whose inactivation suppressed hydroxyisocaproate dehydrogenase activity, was cloned and overexpressed in Escherichia coli , and the recombinant His-tagged fusion protein was purified and characterized. The gene annotated panE was the sole gene responsible for the reduction of the 2-keto acids derived from leucine, isoleucine, and valine, while ldh , encoding l -lactate dehydrogenase, was responsible for the reduction of the 2-keto acids derived from phenylalanine and methionine. The kinetic parameters of the His-tagged PanE showed the highest catalytic efficiencies with 2-ketoisocaproate, 2-ketomethylvalerate, 2-ketoisovalerate, and benzoylformate ( V max / K m ratios of 6,640, 4,180, 3,300, and 2,050 U/mg/mM, respectively), with NADH as the exclusive coenzyme. For the reverse reaction, the enzyme accepted d -2-hydroxyacids but not l -2-hydroxyacids. Although PanE showed the highest degrees of identity to putative NADP-dependent 2-ketopantoate reductases (KPRs), it did not exhibit KPR activity. Sequence homology analysis revealed that, together with the d -mandelate dehydrogenase of Enterococcus faecium and probably other putative KPRs, PanE belongs to a new family of d -2-hydroxyacid dehydrogenases which is unrelated to the well-described d -2-hydroxyisocaproate dehydrogenase family. Its probable physiological role is to regenerate the NAD + necessary to catabolize branched-chain amino acids, leading to the production of ATP and aroma compounds.

Publisher

American Society for Microbiology

Subject

Molecular Biology,Microbiology

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