Low temperature synthesis of magnetite and maghemite nanoparticles

We report on the synthesis of iron oxide nanoparticles below 100 degrees C by a simple chemical protocol. The uniqueness of the method lies in the use of Ferrous ammonium sulphate (in conjugation with FeCl3) which helps maintain the stability of Fe2+ state in the reaction sequence thereby controlling the phase formation. Hexamine was added as the stabilizer. The nanoparticles synthesized at three different temperatures viz, 5 degrees, 27 degrees, and 95 degrees C are characterized by several techniques. Generally, when a mixture of Fe3+ and Fe2+ is added to sodium hydroxide, alpha-Fe2O3 (the anti-ferromagnetic phase) is formed after the dehydration process of the hydroxide. In our case however, the phases formed at all the three temperatures were found to be ferro (ferri) magnetic, implying modification of the formation chemistry due to the specifics of our method. The nanoparticles synthesized at the lowest temperature exhibit magnetite phase, while increase in growth temperature to 95 degrees C leads to the maghemite phase.     

Cold plasma for the preservation of aquatic food products: An overview

Cold plasma (CP) is an upcoming technology implemented for the preservation of highly perishable foods, especially aquatic food products (AFPs). The high moisture content, high-quality protein with all essential amino acids and unsaturated fatty acids makes AFP more susceptible to microbial spoilage and oxidation of lipids and proteins. Spoilage lowers the nutritive value and could generate toxic components, making it unsafe for consumption. In recent times, the rising demand for food products of aquatic origin with preserved quality and extended shelf-life has been recorded. In addition, minimally or nonthermally processed and preserved foods are gaining great attention. CP technology has demonstrated an excellent ability to inactivate microorganisms without promoting their resistance and triggering some deteriorative enzymes, which are typical factors responsible for the spoilage of AFP. Consequently, CP could be recommended as a minimal processing intervention for preserving the quality of AFP. This review focuses on different mechanisms of fish spoilage, that is, by microorganisms and oxidation, their inhibition via the application of CP, and the retention of quality and shelf-life extension of AFP.     

Protein characteristics and peroxidase activities of different Indian wheat varieties and their relationship to chapati-making quality

Different wheat varieties grown at a single geographical location were evaluated for protein quantity and quality, rheological properties, and activities of peroxidase as well as polyphenol oxidase. The protein content in these varieties ranged from 11.6 to 14.6%, farinograph water absorption ranged from 70 to 76%, and the damaged starch content varied from 12.3 to 16.3%. The total protein content of whole wheat flours significantly correlated to stiffness (R/E values) of the dough (r=0.73, p<0.05); however, it did not influence any of the quality parameters of chapati. However, the protein quality parameter, Glu-1 score, which reflects the high molecular weight (HMW) glutenin subunit composition, correlated significantly to the cutting force, which indicates the texture of chapati (r=0.78, p<0.05). The quantity of low molecular weight protein fraction having molecular weight of 20 kDa showed significant correlation to over all quality scores of chapati (r=0.78, p<0.05). The color of chapatis was significantly correlated to color of dough (r=0.76, p<0.05), which became darker on resting. Peroxidase activity greatly influenced the color of chapatis (r=0.81, p<0.05).     

Detection of Listeria monocytogenes in Fresh Produce Using Molecular Beacon—Real‐time PCR Technology

ABSTRACT: The capability of an assay to detect Listeria monocytogenes from artificially inoculated fresh‐cut produce such as cantaloupe and mixed salad was demonstrated. An oligonucleotide probe that becomes fluorescent upon hybridization to the target DNA (Molecular Beacon, MB) was used in a real‐time polymerase chain reaction (PCR) assay. As few as 4 to 7 colony‐forming units (CFU) of L. monocytogenes per 25 g of artificially contaminated produce could be detected. A comparison of 2 commercially available kits using MB‐PCR (iQ‐Check, Bio‐Rad Laboratories) and conventional PCR (BAX, Dupont Qualicon) was performed on artificially inoculated produce. The time required to detect L. monocytogenes (from produce to PCR) was considerably shorter for the iQ‐Check protocol (approximately 26 h) compared with the BAX‐PCR (approximately 52 h). The iQ‐Check protocol was also used to confirm the identity of the L. monocytogenes isolates obtained during a microbiological screen of conventional and organic leaf lettuce and alfalfa sprout samples from local supermarkets. The iQ check protocol was successful in differentiating L. monocytogenes isolates from other Listeria spp. such as L. welshimeri, L. innocua, and L. ivanovii. This is the 1st report of the application of the MB probe being used for real‐time detection of L. monocytogenes in whole and fresh‐cut produce.