Trichoderma longibrachiatum

About: Trichoderma longibrachiatum is a research topic. Over the lifetime, 452 publications have been published within this topic receiving 10591 citations.

Nano-encapsulation of naringinase produced by Trichoderma longibrachiatum ATCC18648 on thermally stable biopolymers for citrus juice debittering.

Abstract: Characteristics of naringinase nano-encapsulated forms on different carrier materials (chitosan and alginate polymers) were investigated in this study. Screening of twelve fungal isolates for naringinase production indicated that Trichoderma longibrachiatum was the most promising. Grapefruit rind was used as a substrate containing naringin for naringinase production. TEM micrographs showed that chitosan nano-capsules were applied for the production of morphologically homogeneous enzymatic nano-particles with high enzyme encapsulation efficiency, small asymmetric sizes (from 15.09 to 27.07 nm with the mean of 21.8 nm) and rough surfaces compared to nano-encapsulated naringinase in alginate which showed nano-particle size (from 33.37 to 51.01 nm with the mean of 43.03 nm). It was revealed that the highest naringinase activity was found in case of chitosan nano-capsule naringinase compared to alginate nano-capsule one. Thermogram analysis (TGA) showed that the free enzyme loses about 92% of its weight at approximately 110°C, while the nano-encapsulated ones show more stability at higher temperatures. Conclusively, the nano-capsulation process improves the kinetics and operational stability so could be useful as a debittering agent for various thermal processing applications in citrus juices industries which makes the fruit juice more acceptable and cost-effective to the consumer.

Sustainable use of the spent mushroom substrate of Pleurotus florida for production of lignocellulolytic enzymes

Abstract: Spent mushroom substrate (SMS), a major byproduct of the mushroom industry, is a lignocellulosic biomass, which contains approximately 57-74.3% of holocellulose fraction. This study was aimed at utilizing SMS of Pleurotus florida for recovery of lignocellulolytic enzymes and sugars and also as a substrate for production of cellulolytic enzymes using different isolates of Trichoderma and Aspergillus under solid-state fermentation (SSF). SMS of P. florida extracts contained significant amounts of laccase (3,015.8 ± 29.5 U/g SMS) and xylanase (1,187.9 ± 12 U/g SMS) activity. Crystallinity pattern and chemical changes in SMS revealed that SMS had a lower crystallinity index (34.2%) as compared with the raw biomass (37.8%), which, in turn, helps in enhancing the accessibility of cellulolytic enzymes to holocellulose. Among the isolates, Trichoderma longibrachiatum A-01 showed maximum activity of endoglucanase (220.4 ± 5.9 U/mg), exoglucanase (78.5 ± 3.2 U/mg) and xylanase (1,550.4 ± 11.6 U/mg) while Aspergillus aculeatus C-08 showed maximum activity of cellobiase (113.9 ± 3.9 U/mg). Extraction with sodium citrate buffer (pH 4.8) showed maximum cellulolytic enzyme activity as compared with other solvents tested. Partial purification of endoglucanase, exoglucanase, xylanase, and cellobiase resulted in 56.3% (1,112.5 U/mg), 48.4% (212.5 U/mg), 44% (4,492.3 U/mg), and 62% (705.0 U/mg) yield with an increase by 5.2-, 4.5-, 4.1-, and 5.0-fold as compared with crude extract. The results reveal that SMS from P. florida could be a potential and cost-effective substrate for production of cellulolytic enzymes from T. longibrachiatum A-01 and A. aculeatus C-08.

Optimum Concentrations of Trichoderma longibrachiatum and Cadusafos for Controlling Meloidogyne javanica on Zucchini Plants

Abstract: A factorial experiment was established in a completely randomized design to verify the effect of different inoculum levels of an Iranian isolate of Trichoderma longibrachiatum separately and in combination with various concentrations of cadusafos against Meloidogyne javanica in the greenhouse Zucchini seeds were soaked for 12 hr in five densities (0, 10(5), 10(6), 10(7), and 10(8) spores/ml suspension) of the fungus prior to planting in pots containing four concentrations of cadusafos (0, 05, 1, and 2 mg ai/kg soil) The data were analyzed using a custom response surface regression model and the response surface curve and contour plots were drawn Reliability of the model was examined by comparing the result of new experimental treatments with the predicted results The optimal levels of these two variables also were calculated The interactive effects of concentrations of Trichoderma and cadusafos were insignificant for several responses such as the total number of eggs per gram soil, the number of intact eggs per gram soil, nematode reproduction factor, and control percent Closeness of experimental mean values with the expected values proved the validity of the model The optimal levels of the cadusafos concentration and Trichoderma concentration that caused the best plant growth and lowest nematode reproduction were 17 mg ai/kg soil and 10(8) conidia/ml suspension, respectively

Trichoderma species from fumigated douglas-fir roots decayed by phellinus weirii

Abstract: Seven species aggregates of Trichoderma and Gliocladium virens were isolated from roots of Phellinus weirii-infested Douglas-fir stumps fumigated with chloropicrin, Vorlex, or methylisothiocyanate, or left untreated. Most commonly isolated was Trichoderma viride, followed by T. hamatum, T. citrinoviride, G. virens, T. polysporum, T. saturnisporum, T. harzianum, and T. longibrachiatum. Roots from chloropicrin-treated stumps were more frequently colonized than those from untreated stumps, although T. citrinoviride was more frequently found in untreated stumps.

Biocontrol of Cytospora canker of poplar in north‐east China with Trichoderma longibrachiatum

Abstract: Summary Trichoderma isolate T05, collected and isolated from a poplar (Populus simonii × Populus nigra) stand in the province of Heilongjiang, China, was tested for its efficacy in controlling Cytospora chrysosperma in vitro and Cytospora canker of poplar in the field. Trichoderma isolate T05 was identified as Trichoderma longibrachiatum in sect. Longibrachiatum based on both morphological characteristics and phylogenetic analysis of the nuclear ribosomal internal transcribed spacer (ITS1 and ITS2) oligonucleotide sequences and the short intron of tef1. During dual culturing, the inhibitory effect of T. longibrachiatum T05 on C. chrysosperma increased over time, and inhibition up to 81% was observed 120 h after inoculation. Hyphae of T. longibrachiatum T05 grew alongside, coiled and sporulated around the pathogen hyphae, which were generally observed to be wrinkled, collapsed, disrupted and degraded. Culture filtrates of T. longibrachiatum T05 that were sterilized by either bacterial filtration or autoclaving suppressed the growth of the pathogen colony. Filtrate sterilized by filtration showed greater inhibitory activity than the autoclaved filtrate, which still had some inhibitory activity, demonstrating that some inhibitory substances were heat unstable and some heat stable. Cytospora chrysosperma C01 colony growth was also reduced by volatile antibiotics produced by T. longibrachiatum T05, with inhibition of 54% observed after 96 h. In a field trial, Cytospora canker on poplar trunks was controlled with efficacy similar to that of routine chemical control by applying a T. longibrachiatum preparation.