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Toxic metalloids including arsenic (As) can neither be eliminated nor destroyed from environment; however, they can be converted from toxic to less/non-toxic forms. The form of As species and their concentration determines its toxicity in plants. Therefore, the microbe mediated biotransformation of As is crucial for its plant uptake and toxicity. In the present study the role of As tolerant Trichoderma in modulating As toxicity in chickpea plants was explored. Chickpea plants grown in arsenate spiked soil under green house conditions were inoculated with two plant growth promoting Trichoderma strains, M-35 (As tolerant) and PPLF-28 (As sensitive). Total As concentration in chickpea tissue was comparable in both the Trichoderma treatments, however, differences in levels of organic and inorganic As (iAs) species were observed. The shift in iAs to organic As species ratio in tolerant Trichoderma treatment correlated with enhanced plant growth and nutrient content. Arsenic stress amelioration in tolerant Trichoderma treatment was also evident through rhizospheric microbial community and anatomical studies of the stem morphology. Down regulation of abiotic stress responsive genes (MIPS, PGIP, CGG) in tolerant Trichoderma + As treatment as compared to As alone and sensitive Trichoderma + As treatment also revealed that tolerant strain enhanced the plant's potential to cope with As stress as compared to sensitive one. Considering the bioremediation and plant growth promotion potential, the tolerant Trichoderma may appear promising for its utilization in As affected fields for enhancing agricultural productivity., (Copyright © 2017 Elsevier Ltd. All rights reserved.)

β-Glucosidases are of pivotal importance in bioconversion of carbonic biomass into fermentable and other useful metabolites, food industry, biotransformation, glyco-trimming of metabolome, etc. Trichoderma citrinoviride when grown on delignified Lantana camara produced a β-glucosidase and secreted it out in the medium. The extracellularly secreted β-glucosidase of T. citrinoviride was homogeneity purified and then characterized for its kinetic properties and proteomic characteristics. The 90 kDa enzyme was monomeric in nature, optimally active at pH 5.5 and the catalytic reaction rate was highest at 55°C. Uniquely, the enzyme was insensitive to inhibition by glucose (up to 5 mM). It also possessed catalytic ability of transglycosylation, as it could catalyze conversion of geraniol into its glucoside. MALDI-TOF assisted proteomic analysis revealed its high degree of sequence similarity with family 3 glycoside hydrolases.

Capabilities of cellulase production, using delignified bioprocessings of medicinal and aromatic plants, viz. citronella (Cymbopogon winterianus) and Artemisia annua (known as marc of Artemisia) and garden waste (chiefly containing Cynodon dactylon), by the six species of Trichoderma were comparatively evaluated. Among the members of Trichoderma studied, T. citrinoviride was found to be the most efficient producer of cellulases along with a high level of beta-glucosidase (produced 102.4 IU g(-1) on marc of Artemisia; 101.33 IU g(-1) on garden waste; 81.86 IU g(-1) on distillation waste of citronella and 94.77 IU g(-1) on pure cellulose). Although T. virens was noticed to be the minimal enzyme producer fungus, it interestingly could not produce complete cellulase enzyme complex on any test waste or pure cellulose, except on marc of Artemisia, where it produced all three enzymes of the complex. Immediate reduction in pH was also noticed during fermentation in the case of pure polymer (cellulose) by all tested fungi, while it was delayed with delignified agrowastes. The pH profile varied with the substrate used as well as with individual species of Trichoderma. On the other hand, no alteration in pH with any species of Trichoderma was noticed when grown on marc of A. annua, which might be due to the buffering capacity of this marc.

Considering importance of a microbial strain capable of increased cellulases production and insensitive to catabolite repression for industrial use, we have developed a mutant strain of Trichoderma citrinoviride by multiple exposures to EMS and ethidium bromide. The mutant produced 0.63, 3.12, 8.22 and 1.94 IU ml(-1) FPase, endoglucanase, beta-glucosidase and cellobiase, respectively. These levels were, respectively, 2.14, 2.10, 4.09 and 1.73 fold higher than those in parent strain. Glucose (upto 20 mM) did not repress enzyme production by the mutant under submerged fermentation conditions. In vitro activity assay with partially purified cellulase showed lack of inhibition by glucose. Interestingly, the partially purified endoglucanase and beta-glucosidase were activated by 2.0 fold and 2.6 fold, respectively, by 20 mM and 30 mM ethanol in the assay mixture. Genetic distinction of the mutant was revealed by the presence of two unique amplicans in comparative DNA fingerprinting performed using 20 random primers.

Abstract: The production of cellulases by Trichoderma citrinoviride fermented on marc of Artemisia annua, and bioconversion of the same marc by produced cellulase system was studied. The effects of pretreatments, substrate concentration, particle size, initial pH, temperature and concentration of the medium components on production of FPase, endoglucanase and β-glucosidase were monitored and comparatively evaluated. Among the three pretreatment processes, alkali hydrolysis with autoclaving was found to be most suitable for production of all the three enzymes. Optimum production of FPase, endoglucanase and β-glucosidase was obtained at 96 h, 96 h and 72 h of fermentation period, respectively. Substrate concentration of 1% with particle size between 200 μm and 475 μm gave the higher yields. Higher production of all the three enzymes was obtained with initial pH value of 5.5, temperature of 28 °C and 75% of mineral salt solution. Partially purified enzyme system obtained by optimized fermentation procedure, was applied for saccharification. Forty six percent of saccharification was noticed after 48 h of incubation on alkali hydrolyzed and autoclaved substrate which was 3.26 fold more than that of unpretreated substrate. [Copyright &y& Elsevier]

Cornmint (Mentha arvensis) is cultivated to produce essential oil, which consists of about 75% of menthol. Fresh biomass is hydrodistilled for ∼5 h to obtain essential oil (1%), and the rest of the pre-treated biomass (99%) is generated as waste. A novel, green and economical two-step process has been developed using a mixture of imidazole (IM:1 M)-p-toluene sulfonic acid (pTSA:1.2 M), and IM (0.2 M)-20%NH 3 for the separation of lignin and hemicellulose, respectively. The lignin and hemicellulose were isolated from the respective solution by precipitation, and final undissolved solid residue was obtained as cellulose. This process was scaled-up, recovering cellulose (38%), hemicellulose (27%), and lignin (14%) using 7 L double jacketed reactor. The processing parameters such as temperature, solvent ratio, and time were optimized using single factorial design mathematical model for the isolation of biopolymers. Further, cellulose was enzymatically biotransformed to glucose through submerged and solid-state fermentation (SSF) using Trichoderma reesei, T. harzianum (TH, TH10) , and T. atroviride. Isolated cellulose was produced 61.5% of glucose at 30 °C, pH 5 in 72 h through SSF process using TH10 strain. This glucose solution was transformed to methyl levulinate (74%) under aqueous-methanol (5:1) solvent system for 2 h at 160 °C using La(OTf) 3.H 2 O catalyst. [Display omitted] [ABSTRACT FROM AUTHOR]