Large CO2 reduction and enhanced thermal performance of agro-forestry, construction and demolition waste based fly ash bricks for sustainable construction.

The exhaust gases in production of burnt clay bricks is responsible for greenhouse gases (GHGs) emission which increase the carbon footprint in the ecosystem. Here, we report carbon emission and thermal performance based evaluation of 8 ft. × 9 ft. × 8 ft. building. The bricks used in building construction are manufactured from fly ash, agro-forestry wastes, construction & demolition wastes (C&D), ground granulated blast furnace slag (GGBFS) using NaOH as activator in order to provide compressive strength in the range of 3-6 MPa with ambient curing at 30 °C for 28 days. Life cycle analysis (LCA) reveals the total CO2 emission for fly ash and burnt clay bricks estimated to be 43.28 gCO2 and 290 gCO2 per brick, respectively. Considering the current scenario, by replacing 1-2% of brunt clay bricks with agro-forestry waste, C&D waste based fly ash bricks can potentially reduce 0.5-1.5 million tons of CO2 emission annually. The embodied energy calculation shows fly ash based bricks consumes 10-15 times less energy as compared to burnt clay bricks. Thermal paremeters viz., U-value (0.5-1.2 W/m2K), thermal conductivity (0.4-0.5 W/mK) show adequate insulation of agro-forestry waste based fly ash bricks highlighting its importance of thermal comfort, CO2 reduction along with sustainable and eco-friendly construction practices.

Investigation of agro-forestry and construction demolition wastes in alkali-activated fly ash bricks as sustainable building materials.

Production of burnt clay bricks, cement and burning of agricultural/forestry wastes are responsible for major greenhouse gases emission. The present work investigate the effect of treated rice straw and forestry leaves in alkali-activated fly ash bricks with construction & demolition wastes for non-load bearing partitions walls at elevated temperature of 800 °C. 1-4 wt% incorporated agro-forestry wastes fly ash bricks with 10 and 20 wt% ground granulated blast slag (GGBFS) addition shows compressive strength ranging from 8 to 15 MPa. The thermal conductivity of the panels with 1-4 wt% agro-forestry addition varies from 0.4 to 0.5 W/m.K. The sound transmission class (STC) of 20 mm thick agro-forestry waste fly ash samples depict moderate sound insulation properties over the range of 24 to 37 dB. The wallette units of burnt clay bricks and agro-forestry based fly ash bricks show load carrying capacity of 360 kN, 273 kN and 195 kN, 110 kN at temperatures of 35 °C and 800 °C respectively. The present study shows a potential green solution toward sustainable building materials in construction sector leading to reduced depletion of fertile soil used in production of burnt clay bricks.

Solidification/stabilisation of Pb (II) and Cu (II) containing wastewater in cement matrix.

This study reported solidification/stabilisation of lead and copper-laden fly ash (adsorbent) utilising cement as binder for their ultimate disposal. The Pb (II) and Cu (II) loaded fly ash was successfully immobilised within the cement matrix without presence of any chemical agents. A retardation of 80-100 min in the setting time of cement paste was noticed on the addition of metal-laden fly ash attributed to the presence of metal ions. However, a gradual decrease in mechanical strength of the mortars was observed with higher amounts of Pb (II) and Cu (II)-loaded fly ash in the mix composition. This decrease is ascribed to the breakdown of calcium silicate hydrate (CSH) gel network in the presence of metal crystallites, as confirmed by scanning electron microscopy (SEM) and energy-dispersive x-ray (EDX) analyses. TG-DTG studies also reveal a decrease in CSH (%) from 4.77% (for fly ash cement mortar) to 4.14% and 3.86% for Pb (II) and Cu (II)-loaded fly ash mortars, respectively. X-ray diffraction (XRD) analysis of metal-laden fly ash cement mortars substantiate the immobilisation of Pb (II) and Cu (II) metal ions in the cement matrix as peaks for Ca[Pb(OH)3]2 and Ca[CuH2O5Si] are visible in their patterns, respectively. TCLP tests conducted on 56 day cured metal-laden fly ash mortars show leachate concentration not exceeding the discharge standards. Overall, these results indicate that this integrated adsorption- solidification/stabilisation process is efficient for safe disposal and utilisation of heavy metal-laden fly ash for building and construction related work as a secondary material.

Performance behaviour of agro-waste based gypsum hollow blocks for partition walls.

Crop residue management is a massive problem in the agriculture sector. Agricultural waste in the form of stubble which is usually burnt in the farm fields, causes severe air pollution and poses a threat to the environment. The present study investigates the addition of agro-waste (rice straw) in gypsum hollow-core blocks for partition walls. Various compositions of agro-waste-based gypsum samples have been studied for compressive strength, thermal, sound absorption, sound transmission loss, and fire-resistant properties. The addition of rice straw in gypsum reduces the density and compressive strength of the test sample, thus making it lightweight for non-load bearing wall application. The thermal conductivity of the rice straw added gypsum samples show a decrease in thermal conductivity from 0.2 to 0.11 W/m K. Acoustic properties viz., noise reduction coefficient (NRC) increases from 25 to 45% with increase in rice straw addition and a decreasing trend in sound transmission class (STC) from 37 to 28 dB. The fire-resistant properties viz., surface spread of flame, and fire propagation index test have shown good fire-resistant properties. The agro-waste-based hollow gypsum blocks may be used as a promising material for drywall partitions owing to its thermal insulation, low density, good acoustic and fire-resistant properties.

Understanding the role of DNA polymerase λ gene in different growth and developmental stages of Oryza sativa L. indica rice cultivars.

DNA polymerase λ (Pol λ) is the only member of DNA polymerase family X present in plants. The enzyme is ddNTP sensitive as it contains the conserved C-terminal Pol ß domain. The 1.1 kb partial coding sequence isolated spanned the whole 3' regions of the gene containing functionally important domains of the Pol λ gene. Comparative in silico studies from both indica and japonica cultivars involving homology modelling showed that the model for the partial Pol λ gene was stable and acceptable. The alignment of both the protein models showed a RMS value of 0.783. Apart from this, expression of Pol λ and its relative activity is studied during different development stages of three different indica rice cultivars (IR29, Nonabokra and N22). Enhanced accumulation and higher activity of Pol λ during the early seedling stage was detected. Higher expression and activity were observed in the anthers, which was probably necessary for DNA repair during microspore formation. However, during the maturation stage of seed development and plant growth, expression and the activity of Pol λ decreased due to slow metabolic activity and a reduced rate of cell division respectively. Furthermore, the expression and activity of Pol λ were found to be higher in IR29 in comparison to Nonabokra and N22. IR29 is a rice cultivar susceptible to environmental stresses and hence it encounters higher DNA damages. The enhanced presence and activity of the Pol λ enzyme in IR29 with respect to the other two cultivars, which are more tolerant to the environmental stresses during various developmental stages, is therefore explainable.

Utilization of plant-derived recombinant human ß-defensins (hBD-1 and hBD-2) for averting salmonellosis.

We describe the use of plant-made ß-defensins as effective antimicrobial substances for controlling salmonellosis, a deadly infection caused by Salmonella typhimurium (referred to further as S. typhi). Human ß-defensin-1 (hBD-1) and -2 (hBD-2) were expressed under the control of strong constitutive promoters in tobacco plants, and bio-active ß-defensins were successfully extracted. In the in vitro studies, enriched recombinant plant-derived human ß-defensin-1 (phBD-1) and -2 (phBD-2) obtained from both T1 and T2 transgenic plants showed significant antimicrobial activity against Escherichia coli and S. typhi when used individually and in various combinations. The 2:1 peptide combination of phBD-1:phBD-2 with peptides isolated from T1-and T2-generation plants reduced the growth of S. typhi by 96 and 85 %, respectively. In vivo studies employing the mouse model (Balb/c) of Salmonella infection clearly demonstrated that the administration of plant-derived defensins individually and in different combinations enhanced the mean survival time of Salmonella-infected animals. When treatment consisted of the 2:1 phBD-1:phBD-2 combination, approximately 50 % of the infected mice were still alive at 206 h post-inoculation; the lowest number of viable S. typhi was observed in the liver and spleen of infected animals. We conclude that plant-made recombinant ß-defensins (phBD-1 and phBD-2) are promising antimicrobial substances and have the potential to become additional tools against salmonellosis, particularly when used in combination.

Effective control of Salmonella infections by employing combinations of recombinant antimicrobial human ß-defensins hBD-1 and hBD-2.

We successfully produced two human ß-defensins (hBD-1 and hBD-2) in bacteria as functional peptides and tested their antibacterial activities against Salmonella enterica serovar Typhi, Escherichia coli, and Staphylococcus aureus employing both spectroscopic and viable CFU count methods. Purified peptides showed approximately 50% inhibition of the bacterial population when used individually and up to 90% when used in combination. The 50% lethal doses (LD50) of hBD-1 against S. Typhi, E. coli, and S. aureus were 0.36, 0.40, and 0.69 µg/µl, respectively, while those for hBD-2 against the same bacteria were 0.38, 0.36, and 0.66 µg/µl, respectively. Moreover, we observed that bacterium-derived antimicrobial peptides were also effective in increasing survival time and decreasing bacterial loads in the peritoneal fluid, liver, and spleen of a mouse intraperitoneally infected with S. Typhi. The 1:1 hBD-1/hBD-2 combination showed maximum effectiveness in challenging the Salmonella infection in vitro and in vivo. We also observed less tissue damage and sepsis formation in the livers of infected mice after treatment with hBD-1 and hBD-2 peptides individually or in combination. Based on these findings, we conclude that bacterium-derived recombinant ß-defensins (hBD-1 and hBD-2) are promising antimicrobial peptide (AMP)-based substances for the development of new therapeutics against typhoid fever.

Isolation, characterization, and structure analysis of a non-TIR-NBS-LRR encoding candidate gene from MYMIV-resistant Vigna mungo.

Yellow mosaic disease of Vigna mungo caused by Mungbean yellow mosaic India virus (MYMIV) is still a major threat in the crop production. A candidate disease resistance (R) gene, CYR1 that co-segregates with MYMIV-resistant populations of V. mungo has been isolated. CYR1 coded in silico translated protein sequence comprised of 1,176 amino acids with coiled coil structure at the N-terminus, central nucleotide binding site (NBS) and C-terminal leucine-rich repeats (LRR) that belongs to non-TIR-NBS-LRR subfamily of plant R genes. CYR1 transcript was unambiguously expressed during incompatible plant virus interactions. A putative promoter-like sequence present upstream of this candidate gene perhaps regulates its expression. Enhanced transcript level upon MYMIV infection suggests involvement of this candidate gene in conferring resistance against the virus. In silico constructed 3D models of NBS and LRR regions of this candidate protein and MYMIV-coat protein (CP) revealed that CYR1-LRR forms an active pocket and successively interacts with MYMIV-CP during docking, like that of receptor-ligand interaction; indicating a critical role of CYR1 as signalling molecule to protect V. mungo plants from MYMIV. This suggests involvement of CYR1 in recognizing MYMIV-effector molecule thus contributing to incompatible interaction. This study is the first stride to understand molecular mechanism of MYMIV resistance.

Molecular marker-assisted genotyping of mungbean yellow mosaic India virus resistant germplasms of mungbean and urdbean.

Mungbean Yellow Mosaic India Virus (MYMIV) belonging to the genus begomovirus causes the yellow mosaic disease in a number of economically important edible grain legumes including mungbean (Vigna radiata), urdbean (Vigna mungo) and soybean (Glycine max). The disease is severe, critical, open spread and inflicts heavy yield losses annually. The objective of this study is to develop molecular markers linked to MYMIV-resistance to facilitate genotyping of urdbean and mungbean germplasms for MYMIV-reaction. Resistance-linked molecular markers were successfully developed from consensus motifs of other resistance (R) gene or R gene homologue sequences. Applying linked marker-assisted genotyping, plant breeders can carry out repeated genotyping throughout the growing season in absence of any disease incidence. Two MYMIV-resistance marker loci, YR4 and CYR1, were identified and of these two CYR1 is completely linked with MYMIV-resistant germplasms and co-segregating with MYMIV-resistant F2, F3 progenies of urdbean. The present study demonstrated that these two markers could be efficiently employed together in a multiplex-PCR-reaction for genotyping both V. mungo and V. radiata germplasms from field grown plants and also directly from the seed stock. This method of genotyping would save time and labour during the introgression of MYMIV-resistance through molecular breeding, as methods of phenotyping against begomoviruses are tedious, labour and time intensive.