Biological control is being considered as an alternative or a supplemental way of reducing the use of chemicals in agriculture. An endophytic strain G3 with potential as a biocontrol agent was isolated from the stems of Triticum aestivum L. It was classified by 16S rDNA sequencing as a member of Serratia. Strain G3 displayed a broad spectrum of antifungal activity in vitro against a number of phytopathogens such as Botrytis cinerea, Cryphonectria parasitica, Rhizoctonia cerealis and Valsa sordida. Molecular mechanisms involved in biocontrol by Serratia sp. G3 was investigated for its potential application to plant health management. The results showed that G3 produces an array of antimicrobial exoproducts, including chitinase, protease, antibiotic pyrrolnitrin, and siderophores for iron competition. Moreover, it also produced the plant growth hormone indole-3-acetic acid, suggesting that multiple mechanisms and their synergistic effects may be involved in biocontrol of plant diseases. Additionally, strain G3 can produce at least ten N-acyl homoserine lactones (AHLs) signal molecules for cell to cell communication, including unsubstituted, 3-oxo, and 3-hydroxy at the C3 position through liquid chromatography-tandem mass spectrometry (LC-MS/MS), which is different from the previously reported Serraia species. For the first time, N-3-oxo-heptanoyl-homoserine lactone, one of the main molecules was reported in the genus Serratia. The role of AHL-dependent quorum sensing system in the interactions between the endophytic strain G3 and host plants and its potential application in improving biocontrol efficacy will be further explored.
As a common waterfront and wet environment tree species, Salix babylonica shows a great potential for restoration of contaminated water or soil environments, such as phenol-polluted water. However, studies on such remediation effects have not been carried out yet. The objective of this study was to investigate the effects of phenols on photosynthesis of S. babylonica. Photosynthetic and chlorophyll fluorescence parameters of S. babylonica cuttings were determined in hydroponic experiment, where six phenol concentrations was used (0, 50, 100, 200, 400, and 800 mg L -1 ). Phenol presence inhibited photosynthesis of S. babylonica significantly, as the net photosynthetic rate (P N ), light-saturated net photosynthetic rate, apparent quantum yield, maximal quantum yield of PSII photochemistry, and effective quantum yield of PSII photochemistry declined significantly. The higher the concentration of phenol solution, the greater inhibition of photosynthesis occurred. Our data indicated that nonstomatal limitation was responsible for the reduction of P N . S. babylonica should be used to remediate phenol-contaminated water, when the concentration of phenol solution is lower than 200 mg L -1 . Otherwise, the efficiency of photosynthesis of S. babylonica would decrease markedly. However, further study is needed to determine the maximum concentration of phenol that S. babylonica can tolerate to maintain normal photosynthetic activity.
Aims: A new cellobiohydrolase (CBH) gene (cbh3) from Chaetomium thermophilum was cloned, sequenced and expressed in Pichia pastoris.
Methods and Results: Using RACE‐PCR, a new thermostable CBH gene (cbh3) was cloned from C. thermophilum. The cDNA of the CBH was 1607 bp and contained a 1356 bp open reading frame encoding a protein CBH precursor of 451 amino acid residues. The mature protein structure of C. thermophilum CBH3 only comprises a catalytic domain and lacks cellulose‐binding domain and a hinge region. The gene was expressed in P. pastoris. The recombinant CBH purified was a glycoprotein with a size of about 48·0 kDa, and exhibited optimum catalytic activity at pH 5·0 and 60 °C. The enzyme was more resistant to high temperature. The CBH could hydrolyse microcrystalline cellulose and filter paper.
Conclusions: A new thermostable CBH gene of C. thermophilum was cloned, sequenced and overexpressed in P. pastoris.
Significance and Impact of the Study: This CBH offers an interesting potential in saccharification steps in both cellulose enzymatic conversion and alcohol production.
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