Functions of the nicotinamide adenine dinucleotide phosphate oxidase family in G anoderma lucidum : an essential role in ganoderic acid biosynthesis regulation, hyphal branching, fruiting body development, and oxidative‐stress resistance
G anoderma lucidum has drawn worldwide interest with regard to its secondary metabolism and pharmaceutical activity. However, the development of such research has been limited because of a lack of basic biological knowledge. Nicotinamide adenine dinucleotide phosphate oxidases (Nox) have recently be...
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Veröffentlicht in: | Environmental microbiology 2014-06, Vol.16 (6), p.1709-1728 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | G
anoderma lucidum
has drawn worldwide interest with regard to its secondary metabolism and pharmaceutical activity. However, the development of such research has been limited because of a lack of basic biological knowledge. Nicotinamide adenine dinucleotide phosphate oxidases (Nox) have recently been highlighted because of the many important biological roles in plants and animals; however, the exact functions of
Nox
are still not fully understood in fungi. In this study, we identified two
N
ox isoforms (
NoxA
and
NoxB
) and a regulator,
NoxR
.
RNA
interference was used, and silencing of the
Nox
isoforms and
NoxR
expression indicated a central role for these genes in hyphal branching, fruiting body development, reactive oxygen species (
ROS
) generation,
ROS
resistance and ganoderic acid biosynthesis regulation. Further mechanistic investigation revealed that
N
ox‐generated
ROS
elevated cytosolic
Ca
2+
levels by activating a plasma membrane
Ca
2+
influx pathway, thereby inducing the
Ca
2+
signal pathway to regulate ganoderic acid biosynthesis and hyphal branching. Importantly, our results highlight the
N
ox functions in signal crosstalk between
ROS
and
Ca
2+
, and these findings provide an excellent opportunity to identify the potential pathway linking
ROS
networks to calcium signalling in fungi and suggest that plants, animals and fungi share a conserved signal‐crosstalk mechanism. |
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ISSN: | 1462-2912 1462-2920 |
DOI: | 10.1111/1462-2920.12326 |