Publications by authors named "Sanath Kondaveeti"

Article Synopsis
  • An NAD-dependent xylitol dehydrogenase, referred to as AfXDH, was cloned and expressed, revealing a gene sequence of 1,110 bp that encodes a protein of 369 amino acids and a molecular mass of approximately 38.9 kDa.
  • AfXDH preferentially uses sorbitol and xylitol as substrates, showing optimal activity in a specific buffer at pH 9.5 and 50°C, and requires Zn or Mn for function.
  • The enzyme demonstrated higher stability and performance compared to other xylitol dehydrogenases, and when paired with NADH oxidase, it efficiently converted xylitol to l-xylulose with a 97% yield,
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The dependency on non-renewable fossil fuels as an energy source has drastically increased global temperatures. Their continuous use poses a great threat to the existing energy reserves. Therefore, the energy sector has taken a turn toward developing eco-friendly, sustainable energy generation by using sustainable lignocellulosic wastes, such as rice straw (RS).

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Anaerobic digestion (AD) serves as a potential bioconversion process to treat various organic wastes/wastewaters, including sewage sludge, and generate renewable green energy. Despite its efficiency, AD has several limitations that need to be overcome to achieve maximum energy recovery from organic materials while regulating inhibitory substances. Hence, bioelectrochemical systems (BESs) have been widely investigated to treat inhibitory compounds including ammonia in AD processes and improve the AD operational efficiency, stability, and economic viability with various integrations.

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In this study, the medium requirements to increase the production of xylitol by using (CT) have been investigated. The technique of single addition or omission of medium components was applied to determine the nutritional requirements. The addition of amino acids such as Asp, Glu, Gln, Asn, Thr, and Gly had no significant effect on CT growth.

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Enhanced covalent immobilization of xylanase from Chaetomium globosum (XylCg) onto SiO nanoparticles was achieved by the modification of surface residues. The mutation of surface residues to lysine by site-directed mutagenesis increased the immobilization efficiency (IE) and immobilization yield (IY). The immobilized mutant XylCg (N172K-H173K-S176K-K133A-K148A) exhibited an IY of 99.

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In this study, chitosan modified with glutaraldehyde (GLA), 3-aminopropyltriethoxysilane (APTES), polyethyleneimine, and APTES followed by GLA (APTES-GLA) as a support material was used to improve methanol production from biogas. Among these support materials, chitosan-APTES-GLA showed the highest increase in immobilization yield and relative efficiency of Methylomicrobium album up to 56.4% and 97.

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Methanol production by co-culture of methanotrophs and was examined from methane, a greenhouse gas. Co-culture exhibited higher methanol yield of 4.72 mM at optimum ratio of and (3:2) compared to individual cultures.

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A novel cellobiohydrolase (CBH)-generating fungi have been isolated and categorized as KMJ820 based on morphology and rDNA gene sequence. Cellulose powder was used as carbon source, the total enzyme activity was 11.51 U/ml is noted; which is among the highest amounts of CBH-generating microbes studied.

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Microbial fuel cells (MFCs) are envisioned as an evolving cost-effective process for treating organic wastes to simultaneously generate bioelectricity. Therefore, in present study a single chambered mediator- less air cathode MFC was operated for bioelectricity generation using citrus waste (CW) as a feedstock. The MFC was operated at four organic loading conditions (OLs; 3, 6, 9 and 12 kg/m).

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The use of lignocellulosic biomass such as rice straw can help subsidize the cost of producing value-added chemicals. However, inhibitory compounds, such as phenolics, produced during the pre-treatment of biomass, hamper the saccharification process. Laccase and electrochemical stimuli are both well known to reduce phenolic compounds.

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The reduction of nitrogen compounds in aqueous solution is extremely important for sustainable management of ecosystem and human health. An autotrophic bioelectrochemical denitrification (BED) process was evaluated at various conditions for enhanced treatment of synthetic wastewater (SW) and ammonium-rich leachate. With SW, a decrease in hydraulic retention time (HRT: 41.

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Labaneh whey (LW) that is rich in residual organics was evaluated for bioelectricity generation using microbial fuel cell (MFC) in two different configurations namely single chamber (MFC-SC) and dual chamber (MFC-DC) MFCs. The whole study was executed in three stages: The first stage evidenced promising amount of bioelectricity generation (DC, 643 mV; SC, 545 mV) along with chemical oxygen demand removal (CODr: DC, 60.63%; SC, CODr: 55.

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Methane (CH) is a well-known and abundant feedstock for natural gas, and is readily available from various sources. In thermal plants, the CH generated from anthropogenic sources is converted into electrical energy via combustion. Microbial fuel cell (MFC) technology has proven to be an efficient strategy for the biological conversion of a many substrates, including biogas (CH), to electricity.

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Algae are autotrophic organisms that are widespread in water bodies. Increased pollution in water bodies leads to eutrophication. However, algae growing in lakes undergoing eutrophication could be utilized towards the generation of added-value bio-electricity using microbial fuel cells (MFCs).

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Electrochemically active anodic biofilm that has adapted under mild applied potentials in the range 100-500 mV was evaluated for its improved bioelectrogenesis and bioelectrochemical treatment of petroleum refinery wastewater (PRW) in a single chamber air cathode microbial fuel cell (MFC). MFC operation with 500 mV as supplemental voltage has exhibited a maximum power density of 132 mW/m, which was three times higher than control MFC (45 mW/m). Similarly, highest substrate removal efficiency (48%) was also obtained with the MFC of 500 mV, followed by 300 mV (37%), 100 mV (32%) and control (27%).

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The performance of a single chamber microbial fuel cell (MFC) with a low-cost polypropylene separator was investigated at various electrode interspaces in a separator electrode assembly (SEA). The lag period was shortened (3.74-0.

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This study evaluates long-term stability of low-cost separators in single-chamber bottle-type microbial fuel cells with domestic wastewater. Low-cost separators tested in this study were nonwoven fabrics (NWF) of polypropylene (PP80, PP100), textile fabrics of polyphenylene sulfide (PPS), sulfonated polyphenylene sulfide (SPPS), and cellulose esters. NWF PP80 separator generated the highest power density of 280 mW/m, which was higher than with ion-exchange membranes (cation exchange membrane; CEM = 271 mW/m, cation exchange membrane; CMI = 196 mW/m, Nafion = 260 mW/m).

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This study proves for the first time the feasibility of biofuel production from anaerobic digestion effluent via bioelectrochemical cell operation at various applied cell voltages (1.0, 1.5 and 2.

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An optimum electrode spacing of less than 1cm was determined for an air cathode microbial fuel cell (MFC) with a membrane electrode assembly (MEA) system. The lag period decreased as the electrode spacing increased and the voltage generation increased. Stable power density increased from 93 mW/m(2) to 248 mW/m(2) when the electrode distance increased from 0mm to 9 mm.

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Electrochemical treatment of nitrate (NO3(-)), nitrite (NO2(-)) and mixtures of nitrate and nitrite was evaluated with microbial catalysts on a cathode in three different bioelectrochemical denitrification systems (BEDS). The removal rates and removal percentage of nitrogen (N) compounds varied during biotic and abiotic operations. The biotic cathode using NO3(-)-N as an electron acceptor showed enhanced removal percentages (88%) compared to the operation with NO2(-)-N (85%).

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Electrochemical treatment of nitrate ions was attempted using different catalysts on the cathode in bioelectrochemical denitrification systems. The carbon cathode coated by biofilm (biocathode) could remove 91 % of nitrate ions at 1.0 V, which was almost same as the Pt-coated electrode (90 %).

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