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  • Regioselectivity of the oxidative C-S bond formation in ergothioneine and ovothiol biosyntheses.

Regioselectivity of the oxidative C-S bond formation in ergothioneine and ovothiol biosyntheses.

Organic letters (2013-09-11)
Heng Song, Maureen Leninger, Norman Lee, Pinghua Liu
ABSTRACT

Ergothioneine (5) and ovothiol (8) are two novel thiol-containing natural products. Their C-S bonds are formed by oxidative coupling reactions catalyzed by EgtB and OvoA enzymes, respectively. In this work, it was discovered that in addition to catalyzing the oxidative coupling between histidine and cysteine (1 → 6 conversion), OvoA can also catalyze a direct oxidative coupling between hercynine (2) and cysteine (2 → 4 conversion), which can shorten the ergothioneine biosynthetic pathway by two steps.

MATERIALS
Product Number
Brand
Product Description

SAFC
L-Histidine
Sigma-Aldrich
L-Histidine, BioUltra, ≥99.5% (NT)
Sigma-Aldrich
L-Histidine, ReagentPlus®, ≥99% (TLC)
Sigma-Aldrich
L-Histidine, suitable for cell culture, meets EP, USP testing specifications, from non-animal source
Sigma-Aldrich
Betaine solution, 5 M, PCR Reagent
Supelco
L-Histidine, certified reference material, TraceCERT®, Manufactured by: Sigma-Aldrich Production GmbH, Switzerland
Supelco
L-Histidine, Pharmaceutical Secondary Standard; Certified Reference Material
Sigma-Aldrich
L-Histidine, Vetec, reagent grade, ≥99%
Sigma-Aldrich
Betaine, ≥98% (perchloric acid titration)
Sigma-Aldrich
L-(+)-Ergothioneine
Sigma-Aldrich
Betaine hydrochloride, ≥99%
Sigma-Aldrich
Betaine, BioUltra, ≥99.0% (NT)