Deletion of admB gene encoding a fungal ADAM affects cell wall construction in Aspergillus oryzae

• Published in: Bioscience, biotechnology, and biochemistry biotechnology, and biochemistry, 2017-05, Vol.81 (5), p.1041-1050
• Main Authors: Kobayashi, Takuji, Maeda, Hiroshi, Takeuchi, Michio, Yamagata, Youhei
• Format: Article
• Language: English
• Subjects: a disintegrin and metalloproteinase; ADAM Proteins - deficiency; ADAM Proteins - genetics; Aspergillus oryzae; Aspergillus oryzae - cytology; Aspergillus oryzae - genetics; Aspergillus oryzae - metabolism; cell wall; Cell Wall - metabolism; Fungal Proteins - genetics; Fungal Proteins - metabolism; Gene Deletion; Gene Expression Regulation, Fungal; Genomics; Kinetics; Phosphorylation; Polysaccharides - metabolism; Transcription, Genetic
• ISSN: 0916-8451; 1347-6947
• DOI: 10.1080/09168451.2016.1270741

Mammals possess a unique signaling system based on the proteolytic mechanism of a disintegrin and metalloproteinases (ADAMs) on the cell surface. We found two genes encoding ADAMs in Aspergillus oryzae and named them admA and admB. We produced admA and admB deletion strains to elucidate their biological function and clarify whether fungal ADAMs play a similar role as in mammals. The ∆admA∆admB and ∆admB strains were sensitive to cell wall-perturbing agents, congo red, and calcofluor white. Moreover, the two strains showed significantly increased weights of total alkali-soluble fractions from the mycelial cell wall compared to the control strain. Furthermore, ∆admB showed MpkA phosphorylation at lower concentration of congo red stimulation than the control strain. However, the MpkA phosphorylation level was not different between ∆admB and the control strain without the stimulation. The results indicated that A. oryzae AdmB involved in the cell wall integrity without going through the MpkA pathway.