Document Type

Article

Journal/Book Title

Biotechnology and Applied Biochemistry

Publication Date

4-8-2019

Publisher

John Wiley and Sons, Inc.

Abstract

Sch47554 and Sch47555 are two angucyclines with antifungal activities against various yeasts and dermatophytes from Streptomyces sp. SCC‐2136. The schgene cluster contains several putative regulatory genes. Both schA4 and schA21were predicted as the TetR family transcriptional regulators, whereas schA16shared significant similarity to the AraC family transcriptional regulators. Although Sch47554 is the major product of Streptomyces sp. SCC‐2136, its titer is only 6.72 mg/L. This work aimed to increase the production of this promising antifungal compound by investigating and manipulating the regulatory genes in the Sch47554 biosynthetic pathway. Disruption of schA4and schA16 led to a significant increase in the production of Sch47554, whereas the titer was dramatically decreased when schA21 was disrupted. Overexpression of these genes gave opposite results. The highest titer of Sch47554 was achieved in Streptomyces sp. SCC‐2136/ΔschA4 (27.94 mg/L), which is significantly higher than the wild type. Our results indicate that SchA4 and SchA16 are repressors, whereas SchA21 acts as an activator. This work thus provides an initial understanding of functional roles of regulatory elements in the biosynthesis of Sch47554. Several efficient producing strains of Sch47554 were constructed by disrupting or over-expressing particular regulatory genes, which can be further engineered for industrial production of this medicinally important molecule.

First Page

1

Last Page

29

Comments

This is the peer reviewed version of the following article: Fidan, Ozkan, et al. “Improved Production of Antifungal Angucycline Sch47554 by Manipulating Three Regulatory Genes in Streptomyces Sp. SCC‐2136.” Biotechnology and Applied Biochemistry, John Wiley & Sons, Ltd, 1 Apr. 2019, iubmb.onlinelibrary.wiley.com/doi/full/10.1002/bab.1748., which has been published in final form at https://doi.org/10.1002/bab.1748 This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions.

Available for download on Wednesday, April 08, 2020

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