Details

Autor(en) / Beteiligte

• Jia, Zhilei
• Yan, Mengdi
• Li, Xiaobei
• Sun, Qiuyan
• Xu, Gen
• Li, Shuai
• Chen, Wenchao
• Shi, Zhimin
• Li, Zhonghai
• Chen, Mei
• Bao, Xiaoming

Titel

Phosducin-like protein PoPlp1 impacts cellulase and amylase expression and development in Penicillium oxalicum via the G protein–cAMP signaling pathway

Ist Teil von

• Frontiers in microbiology, 2023-06, Vol.14, p.1165701-1165701

Ort / Verlag

Frontiers Media S.A

Erscheinungsjahr

2023

Link zum Volltext

Quelle

Free E-Journal (出版社公開部分のみ）

Beschreibungen/Notizen

• In this study, a phosducin-like protein, Po Plp1, was identified and functionally studied in the cellulase-producing strain Penicillium oxalicum 114-2. Po Plp1 was proven to participate in several biological processes, including mycelium development, conidiation, and expression of cellulases and amylases. With deletion of Po plp1, morphology and development varied significantly in Δ Poplp1 . Colony growth, glucose utilization, and the hydrolysis capability of starch and cellulose were limited, whereas conidiation was enhanced. Based on detection of the levels of expression of transcription factors involved in asexual development, we conjectured that Po Plp1 is involved in conidiation via the major factor BrlA. We explored the effect of Po Plp1 on cellulase and amylase expression and observed that cellulase and amylase activity and major gene transcription levels were all dramatically reduced in Δ Poplp1 . Deletion of Po Plp1 caused a decrease in intracellular cAMP levels, and the cellulase gene expression level of Δ Poplp1 was restored to a certain extent through external addition of cAMP. These findings demonstrate that Po Plp1 may affect cellulase and amylase expression by regulating cAMP concentration. To comprehensively explore the mechanism of Po Plp1 in regulating multiple biological processes, we performed a comparative transcriptomic analysis between strains P. oxalicum 114-2 and Δ Poplp1 . The major cellulase and amylase genes were all downregulated, congrent with the results of real-time quantitative polymerase chain reaction analysis. The genes involved in the G protein–cAMP signaling pathway, including several G-protein-coupled receptors, one regulator of G protein signaling, and two cAMP phosphodiesterases, were disrupted by deletion of Po Plp1. These results confirm the positive function of Po Plp1 in the G protein–cAMP signaling pathway. This functional analysis of Po Plp1 will be very beneficial for further study of the regulatory mechanisms of cellulase expression and other biological processes in P. oxalicum 114-2 via the G protein–cAMP signaling pathway.