The predicted protein of this RGC is 1340 amino acids long and belongs to the CC-NBS-LRR subfamily of plant resistance INK 128 datasheet genes. To verify that RGC260 belongs to a functional group of resistance genes, the transcript accumulation of the RGC was detected using real-time PCR following infection of plants with P. helianthi and Plasmopara halstedii, the two major pathogens of sunflower. The expression profile of this RGC revealed that its expression was specifically induced during an incompatible interaction between sunflower and
P. helianthi. Expression profiles of defense genes and component signaling genes proposed the nature of this pathosystem as a gene-for-gene interaction. These results suggest that RGC260 may play a critical role in protecting sunflower cells against P. helianthi. “
“Using universal phytoplasma primer pairs R16mF2/R16mR1 and R16F2n/R16R2, nested polymerase chain reactions were used for phytoplasma detection in Chinese pink HM781-36B solubility dmso with white leaves and stunt symptoms. Sequencing results and restriction fragment length polymorphism (RFLP) analysis of the 1248-bp R16F2n/R16R2 products revealed the phytoplasma belongs to group 16SrV. Phylogenetic analysis showed that the phytoplasma
had a close relation to Jujube Witches-broom phytoplasma. This is the first report of a 16SrV-related phytoplasma infecting Chinese pink in China. “
“The protective effect of autoclaved water extract from spent mushroom substrate (AWESMS) and autoclaved spent mushroom substrate (ASMS) of the
edible mushrooms Lyophyllum decastes (hatakeshimeji) and Pleurotus eryngii (eringi) against fungal and bacterial diseases was investigated on cucumber plants. When the plants were treated with AWESMS by spraying the first true leaves and inoculated with the target pathogen 7 days later, AWESMS pentoxifylline of hatakeshimeji significantly reduced powdery mildew by Podosphaera xanthii, angular leaf spot by Pseudomonas syringae pv. lachrymans, but not Corynespora leaf spot by Corynespora cassiicola and scab by Cladosporium cucumerinum. When the plants were grown in a mixture (1 : 2, v/v) of ASMS of hatakeshimeji and soil, a significant disease reduction was observed in powdery mildew, scab and angular leaf spot. The protective effect was also observed against anthracnose on plants treated with AWESMS or on plants grown in a mixture of ASMS of eringi (1 : 3, v/v). Our results indicated that AWESMS and ASMS, independently of the mushroom type, provide a protective effect against fungal and bacterial diseases. Therefore, SMS should be considered an easily available source of active compounds to protect plants from fungal and bacteria infections, helping alleviate the waste disposal problem in the mushroom industry and creating an environmentally friendly method to reduce plant pathogens.