Identification and distribution of a downregulatory signaling alkyloxazole in <i> <i>Streptomyces</i> </i>

M Michael Madden (Division of Chemical Biology and Medicinal Chemistry, College of Pharmacy, University of Texas at Austin) D Dan Xue (Division of Chemical Biology and Medicinal Chemistry, College of Pharmacy) M Mingming Xu (Division of Chemical Biology and Medicinal Chemistry, College of Pharmacy) K Katherine Holandez-Lopez (Division of Chemical Biology and Medicinal Chemistry, College of Pharmacy, University of Texas at Austin) J Joseph Budiselich (Department of Chemistry and Biochemistry, University of South Carolina) S Sarah Tran (Department of Chemistry and Biochemistry, University of South Carolina) C Cole Espinosa (Department of Chemistry and Biochemistry, University of South Carolina) J Jie Li

Abstract

Streptomyces use small molecules to dictate morphological development and secondary metabolism. Most of these signaling compounds are inducers derived from γ-butyrolactone (GBL)-synthesizing enzymes. As such, biosynthetically distinct and downregulatory signaling molecules remain understudied in Streptomyces . Here, we report the identification of alkyloxaozle (AOX, 1 ), a downregulator of sporulation and antibiotic production in Streptomyces . 1 ’s structure features an oxazole head flanked by an alkyl tail synthesized by a nonribosomal peptide synthetase (NRPS) that has not been reported in Streptomyces signaling molecules. Functional studies found that 1 downregulated sporulation and secondary metabolism in several Streptomyces strains. Genome mining identified 45 homologous biosynthetic gene clusters (BGCs) only distributed in Streptomyces , underscoring the importance of AOXs to this productive genus. Altogether, this report presents a downregulatory class of signaling molecules that broadly affect Streptomyces and highlights their importance to the genus.

Article Details

Volume / Issue Vol. 123, Issue 28
Published July 14, 2026
ISSN 0027-8424
Publisher National Academy of Sciences

Authors (8)

M

Michael Madden

Division of Chemical Biology and Medicinal Chemistry, College of Pharmacy, University of Texas at Austin

D

Dan Xue

Division of Chemical Biology and Medicinal Chemistry, College of Pharmacy

M

Mingming Xu

Division of Chemical Biology and Medicinal Chemistry, College of Pharmacy

K

Katherine Holandez-Lopez

Division of Chemical Biology and Medicinal Chemistry, College of Pharmacy, University of Texas at Austin

J

Joseph Budiselich

Department of Chemistry and Biochemistry, University of South Carolina

S

Sarah Tran

Department of Chemistry and Biochemistry, University of South Carolina

C

Cole Espinosa

Department of Chemistry and Biochemistry, University of South Carolina

J

Jie Li