Matsui, M., Yokoyama, T., Nemoto, K., Kumagai, T., Terai, G., Tamano, K., Machida, M. and Shibata, T. (2017) Identification of a Putative FR901469 Biosynthesis Gene Cluster in Fungal sp. No. 11243 and Enhancement of the Productivity by Overexpressing the Transcription Factor gene frbF. Journal of Bioscience and Bioengineering, 123, 147-153.
https://doi.org/10.1016/j.jbiosc.2016.08.007

has been cited by the following article:

• TITLE: Exploration of Activated Pathways for Improving Antifungal Agent FR901469 Productivity in Fungal Species No.11243 Using Comprehensive Pathway Model

  AUTHORS: Itaru Takeda, Hiroya Itoh, Makoto Matsui, Takashi Shibata, Masayuki Machida, Sachiyo Aburatani

  KEYWORDS: Bioinformatics, Metabolic Pathway Model, Fungi, Secondary Metabolites

  JOURNAL NAME: Journal of Biosciences and Medicines, Vol.5 No.7, July 18, 2017

  ABSTRACT: Secondary metabolites are important for various industrial applications. The production of secondary metabolites is often improved by the activation of substrate supply pathways for biosynthesis. However, many important pathways have remained unclear. In this study, we explored possible pathways related to substrate supply for the biosynthesis of the antifungal agent FR901469 which is a nonribosomal peptide and a fungal secondary metabolite. To clarify the unknown activated pathways, we utilized the Comprehensive Pathway Model (CPM) which was developed in our previous study. We verified that the overexpression of the hypothetical beta-alanine-aminotransferase (BAL-AT), which was included in the explored pathways, improved the FR901469 productivity. The genes encoding the BAL metabolic enzymes are considered to be important for improving the FR901469 productivity.