Antiadhesive activity of poly-hydroxy butyrate biopolymer from a marine Brevibacterium casei MSI04 against shrimp pathogenic vibrios

Vibrio pathogens are causative agents of mid-culture outbreaks, and early mortality syndrome and secondary aetiology of most dreadful viral outbreaks in shrimp aquaculture. Among the pathogenic vibrios group, Vibrio alginolyticus and V. harveyi are considered as the most significant ones in the grow-out ponds of giant black tiger shrimp Penaeus monodon in India. Use of antibiotics was banned in many countries due to the emergence of antibiotic-resistant strains and accumulation of residual antibiotics in harvested shrimp. There is an urgent need to consider the use of alternative antibiotics for the control of vibriosis in shrimp aquaculture. Biofilm formation is a pathogenic and/or establishment mechanism of Vibrio spp. This study aims to develop novel safe antibiofilm and/ or antiadhesive process using PHB to contain vibrios outbreaks in shrimp aquaculture

Growth Study and Biological Hydrogen Production by novel strain Bacillus paramycoides

Industrial revolution has created high dependent on fossil fuels for energy creation. However, combustion of fossil fuels has created excessive amount of greenhouse gases, hence led to climate change. Thus, renewable energy has been proposed to alleviate the environmental pollution issues around the globe. One of the promising renewable energies is green hydrogen energy. Commercialized technologies such as electrolysis and thermochemical reaction are utilized to form hydrogen energy. Nonetheless, these processes require high energy and yet producing greenhouse gases that harm the environment. In this study, biodegradation process to produce hydrogen energy has been explored. To our knowledge, Bacillus paramycoides strain has not yet been investigated for biological hydrogen evolution. Therefore, in this paper, the ability of Bacillus paramycoides to produce biological hydrogen has been studied. The rod-shaped and gram-positive Bacillus paramycoides was identified under scanning electron microscope and gram staining procedure. Furthermore, biological hydrogen generation by Bacillus sp. was experimented for 96 hours. The result shows that 4668 ± 120 ppm cumulative hydrogen gas was generated through dark fermentation process. For Bacillus sp. growth study, lag, log, and stationary phase have been achieved in 96 hours. In a summary, metabolic engineering to degrade abundant biomass wastes is a sustainable pathway to produce hydrogen energy, simultaneously resolve waste management issue around the globe

In-vitro Evaluation of Chitosan - Hydroxyapatite Nanocomposite Scaffolds as Bone Substitutes with Antibiofilm Properties

An opaque, white chitosan/ Hydroxyapatite nanocomposite was prepared by a simple blend method. Morphology, pore size and dispersion of nano-hydroxyapatite in chitosan matrix were visualized using SEM images. The FTIR and SEM with EDX analysis confirmed the bony apatite layer was formed on the outside of the composite. Porosity measurements and water uptake studies of the nanocomposite were evaluated which revealed the maximum porosity of 80% to 92% in the chitosan: hydroxyapatite nanocomposite at the ratio of 20:80. The results also showed that water absorption ability was inversely proportional to the hydroxyapatite present in the nanocomposite. The porosity of prepared nanocomposite was corresponding to the cancellous bone porosity of 50% to 90% suggesting possible applications in bone transplantation. The nanocomposite exhibited antibacterial activity towards the tested Gram-negative and Gram-positive species of bacteria and reduced the bacterial adhesion in biofilm formation

<span style="font-size:15.0pt;mso-bidi-font-size: 12.0pt" lang="EN-GB">Proteolytic enzyme mediated antagonistic potential of <i style="mso-bidi-font-style:normal">Pseudomonas aeruginosa</i> against <i style="mso-bidi-font-style:normal">Macrophomina phaseolina</i> </span>

1024-1031A new antagonistic bacterial strain PGPR2 was isolated from the mungbean rhizosphere and documented for the production of hydrolytic enzymes with antifungal activity. Based on the phylogenetic analysis of the 16S rRNA gene sequence and phenotyping, this strain was identified as Pseudomonas aeruginosa. Maximum protease activity (235 U/mL) was obtained at 24 h of fermentation. The protease was purified to homogeneity in three steps: ammonium sulphate precipitation, anion exchange chromatography on DEAE- cellulose resin and gel filtration chromatography using P6 column. The purified enzyme had a molecular weight of ~33 kDa. The purified protease exhibited maximum activity at pH 6.0 and retained 80% of activity in a pH range of 5.0 - 9.0. Proteolytic activity was maximum in a temperature range of 40–70 °C. However, the enzyme was stable at 40 °C for 60 min. Among the metals tested, Mg2+ enhanced the protease activity. Internal amino acid sequence of the protease obtained by MALDI -ToF and subsequent Mascot database search showed maximum similarity to the HtpX protease of <i style="mso-bidi-font-style: normal">P. aeruginosa strain PA7. Thus, by virtue of its early production time, thermostability and effective antifungal ability, the protease purified and characterized from P. aeruginosa PGPR2 has several potential applications as fungicidal agents in agriculture

Growth Study and Biological Hydrogen Production by novel strain

Industrial revolution has created high dependent on fossil fuels for energy creation. However, combustion of fossil fuels has created excessive amount of greenhouse gases, hence led to climate change. Thus, renewable energy has been proposed to alleviate the environmental pollution issues around the globe. One of the promising renewable energies is green hydrogen energy. Commercialized technologies such as electrolysis and thermochemical reaction are utilized to form hydrogen energy. Nonetheless, these processes require high energy and yet producing greenhouse gases that harm the environment. In this study, biodegradation process to produce hydrogen energy has been explored. To our knowledge, Bacillus paramycoides strain has not yet been investigated for biological hydrogen evolution. Therefore, in this paper, the ability of Bacillus paramycoides to produce biological hydrogen has been studied. The rod-shaped and gram-positive Bacillus paramycoides was identified under scanning electron microscope and gram staining procedure. Furthermore, biological hydrogen generation by Bacillus sp. was experimented for 96 hours. The result shows that 4668 ± 120 ppm cumulative hydrogen gas was generated through dark fermentation process. For Bacillus sp. growth study, lag, log, and stationary phase have been achieved in 96 hours. In a summary, metabolic engineering to degrade abundant biomass wastes is a sustainable pathway to produce hydrogen energy, simultaneously resolve waste management issue around the globe

Biological Hydrogen Energy Production by Novel Strains <i>Bacillus paramycoides</i> and <i>Cereibacter azotoformans</i> through Dark and Photo Fermentation

In daily life, energy plays a critical role. Hydrogen energy is widely recognized as one of the cleanest energy carriers available today. However, hydrogen must be produced as it does not exist freely in nature. Various methods are available for hydrogen production, including electrolysis, thermochemical technology, and biological methods. This study explores the production of biological hydrogen through the degradation of organic substrates by anaerobic microorganisms. Bacillus paramycoides and Cereibacter azotoformans strains were selected as they have not yet been studied for biological hydrogen fermentation. This study investigates the ability of these microorganisms to produce biological hydrogen. Initially, the cells were identified using cell morphology study, gram staining procedure, and 16S ribosomal RNA (rRNA) gene polymerase chain reaction. The cells were revealed as Bacillus paramycoides (MCCC 1A04098) and Cereibacter azotoformans (JCM 9340). Moreover, the growth behaviour and biological hydrogen production of the dark and photo fermentative cells were studied. The inoculum concentrations experimented with were 1% and 10% inoculum size. This study found that Bacillus paramycoides and Cereibacter azotoformans are promising strains for hydrogen production, but further optimization processes should be performed to obtain the highest hydrogen yield