2022
DOI: 10.3390/jof8080779
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RNA-Seq Provides Insights into the Mechanisms Underlying Ilyonectria robusta Responding to Secondary Metabolites of Bacillus methylotrophicus NJ13

Abstract: (1) Background: Ilyonectria robusta can cause ginseng to suffer from rusty root rot. Secondary metabolites (SMs) produced by Bacillus methylotrophicus NJ13 can inhibit the mycelial growth of I. robusta. However, the molecular mechanism of the inhibition and response remains unclear. (2) Methods: Through an in vitro trial, the effect of B. methylotrophicus NJ13’s SMs on the hyphae and conidia of I. robusta was determined. The change in the physiological function of I. robusta was evaluated in response to NJ13’s… Show more

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Cited by 2 publications
(2 citation statements)
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“…Production of cell wall hydrolase is often considered as an important way for biocontrol strain to exert its mycolytic effect (Parmar et al., 2015; Viterbo et al., 2002). It has been discovered that Trichoderma harzianum ‐1 (Ghosh et al., 2015), Streptomyces blastmyceticus JZB130180 (Ni et al., 2019), Bacillus methylotrophicus NJ13 (Li et al., 2022) etc. can produce hydrolytic enzymes to damage the cell structure of target phytopathogens and resulting in mycolysis.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Production of cell wall hydrolase is often considered as an important way for biocontrol strain to exert its mycolytic effect (Parmar et al., 2015; Viterbo et al., 2002). It has been discovered that Trichoderma harzianum ‐1 (Ghosh et al., 2015), Streptomyces blastmyceticus JZB130180 (Ni et al., 2019), Bacillus methylotrophicus NJ13 (Li et al., 2022) etc. can produce hydrolytic enzymes to damage the cell structure of target phytopathogens and resulting in mycolysis.…”
Section: Discussionmentioning
confidence: 99%
“…Conductivity and leakage value of extracellular fluid of the test phytopathogenic fungi were determined with reference to the method of Li et al. (2022) and Xu et al. (2019) respectively: A 9‐mm‐diameter mycelial discs of B. cinerea and A. solani were inoculated individually in LB‐1 culture filtrate (one mycelial disc per 30 mL culture filtrate) and shaking‐cultured (25°C, 130 r/min).…”
Section: Methodsmentioning
confidence: 99%