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. 2019 May 30;16(11):1913. doi: 10.3390/ijerph16111913

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© 2019 by the authors.

Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).

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Agarose gel electrophoresis of the biosynthetic gene amplification products. (A) 1200–1400 bp fragments of polyketide synthase I (PKS-I) genes, (B) 800 to 900 bp fragments of type II polyketide synthase (PKS-II) genes, and (C) 700 bp fragments of non-ribosomal peptide synthase (NRPS) genes. Lane, I: 1 kb molecular weight marker; lane II: Streptomyces parvisporogenes (S2A-04); lane III: Streptomyces manipurensis (S3A-05); lane IV: Streptomyces manipurensis (S3A-09); lane V: non-active strain Streptomyces angustumyceticus S6A-03; and lane VI: Streptomyces coelicolor (control + PKS-I and NRPS).