# Identification of the phosphatase essential for riboflavin biosynthesis in Aquifex aeolicus

## TL;DR

This study identifies a specific phosphatase in Aquifex aeolicus that is essential for riboflavin production, distinguishing it from a nonspecific phosphatase.

## Contribution

The discovery of a histidine family phosphatase specifically involved in riboflavin biosynthesis in Aquifex aeolicus.

## Key findings

- Two phosphatases from Aquifex aeolicus dephosphorylate ARAPDP, but only one supports riboflavin production.
- The histidine family phosphatase specifically dephosphorylates ARAPDP without affecting other substrates.
- X-ray crystallography revealed distinct structural folds for the two phosphatases.

## Abstract

The riboflavin biosynthetic pathway uses dedicated enzymes that function exclusively for riboflavin production. Indeed, the pathway is fully annotated, with the exception of an unknown phosphatase that catalyzes the dephosphorylation of 5-amino-6-ribitylamino-pyrimidinedione 5′-phosphate (ARAPDP) to generate 5-amino-6-ribitylamino-pyrimidinedione (ARAPD), which is the substrate for the penultimate enzyme of the pathway, lumazine synthase. Whereas nonspecific phosphatases from the haloacid dehalogenase superfamily capable of catalyzing the dephosphorylation of ARAPDP have been reported for Bacillus subtilis, Escherichia coli, and Arabadopsis thaliana, we hypothesized that a specific phosphatase may carry out this reaction. Using an anaerobic activity-based screen, two phosphatases from Aquifex aeolicus were identified that dephosphorylate ARAPDP, but only one reconstitutes riboflavin production in a one-pot experiment with the other four enzymes of riboflavin biosynthesis. The first enzyme, annotated as an IMP, is nonspecific, and indiscriminately dephosphorylates ARAPDP along with ribulose 5-phosphate and NADPH, two required substrates of riboflavin biosynthesis. The second enzyme, a histidine family phosphatase, only dephosphorylates ARAPDP in the one-pot experiment thus facilitating riboflavin formation. The structures of both enzymes were determined by X-ray crystallography to reveal the vastly different folds capable of performing the ARAPDP dephosphorylation chemistry. This work has impact both for the production of riboflavin by microbial fermentation and for antimicrobial drug design.