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AaLaeA targets AaFla1 to mediate the production of antitumor compound in Alternaria alstroemeria.

Authors :
Feng, Can
Zheng, Wen
Han, Long
Wang, Jian‐kang
Zha, Xing‐ping
Xiao, Qing
He, Zhang‐jiang
Kang, Ji‐chuan
Source :
Journal of Basic Microbiology; Jan2024, Vol. 64 Issue 1, p68-80, 13p
Publication Year :
2024

Abstract

Endophytic fungi are an important source of novel antitumor substances. Previously, we isolated an endophytic fungus, Alternaria alstroemeria, from the medicinal plant Artemisia artemisia, whose crude extracts strongly inhibited A549 tumor cells. We obtained a transformant, namely AaLaeAOE26, which completely loses its antitumor activity due to overexpression of the global regulator AaLaeA. Re‐sequencing analysis of the genome revealed that the insertion site was in the noncoding region and did not destroy any other genes. Metabolomics analysis revealed that the level of secondary antitumor metabolic substances was significantly lower in AaLaeAOE26 compared with the wild strain, in particular flavonoids were more downregulated according to the metabolomics analysis. A further comparative transcriptome analysis revealed that a gene encoding FAD‐binding domain protein (Fla1) was significantly downregulated. On the other hand, overexpression of AaFla1 led to significant enhancement of antitumor activity against A549 with a sevenfold higher inhibition ratio than the wild strain. At the same time, we also found a significant increase in the accumulation of antitumor metabolites including quercetin, gitogenin, rhodioloside, liensinine, ginsenoside Rg2 and cinobufagin. Our data suggest that the global regulator AaLaeA negatively affects the production of antitumor compounds via controlling the transcription of AaFla1 in endophytic A. alstroemeria. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
0233111X
Volume :
64
Issue :
1
Database :
Complementary Index
Journal :
Journal of Basic Microbiology
Publication Type :
Academic Journal
Accession number :
174763634
Full Text :
https://doi.org/10.1002/jobm.202300319