Assessment of Microbiological Qualities and Iodine Contents of Some Brands of Domestic Salt Available in South-eastern Nigeria

Domestic salt is a food condiment, thus, a veritable tool for food contamination. Salt iodisation provides iodine an essential micronutrient and a key component of the thyroid hormones that regulate vital metabolic activities in the body. Insufficiency of iodine results in iodine deficiency disorders (IDD) which affect the functions of vital organs and systems of the body, leading to damaging effects particularly in pregnancy and early childhood, causing miscarriages, stillbirth, mental retardation, and increased infant mortality. Thirty samples of domestic salt made up of ten each of three popular brands in Nigerian markets were obtained from retail stores and evaluated for microbial qualities and iodine contents. Standard microbiological methods and iodometric titration method were employed for sample analysis. Bacillus and fungal species were isolated after sample pre-enrichment and within counts ( 30 ppm iodine at distributor and retail levels and > 50 ppm iodine at port of entry and salt factory level. This could indicate none compliance to standard specifications. There is need for effective legislation and strict monitoring of food fortification at all levels to ensure compliance to standards and adherence to good manufacturing practices/hazard analysis and quality control precepts which are imperative to effective food fortification programmes

SCREENING AND PARTIAL PURIFICATION OF AMYLASE FROM ASPERGILLUS NIGER ISOLATED FROM DETERIORATED TOMATO (LYCOPERSICON ESCULENTUM MILL.) FRUITS

Amylases (EC 3.2.1.1) are cellwall degrading enzymes associated with the pathogenicity of microorganisms in the spoilage of tomato fruits. The use of amylase in many industries has made it very important to optimize production process to achieve maximum yields. Screening and partial purification of Amylase from Aspergillus niger isolated from tomato (Lycopersicon esculentum Mill.) fruits was studied. Amylase producing fungi were isolated from fresh tomatoes kept at ambient temperature (28±1˚C). Isolates were characterized on the basis of their morphological and cultural techniques. Partial purification of amylase was carried out by ammonium sulphate precipitation. The enzyme activity was determined and optimum conditions were obtained. The molecular weights of the crude and partially purified Amylase were determined by SDS PAGE method. A total of five isolates were obtained using basic screening technique for amylase activity, one of the isolates (Isolate code F2) exhibited maximum amylase activity. The fungi isolate code F2 was identified as Aspergillus niger. Optimum conditions for Amylase AMY F2 were ascertained at pH 6.0; temperature 30°C; substrate concentration of 0.3mg/ml, and time of heating of less than 10min. The molecular weights of the crude and partially purified Amylase AMY F2 were found to be 55kDa and 35kDa respectively by SDS PAGE method. Microorganisms had been an encouraging means of economical production of enzymes in large scale for the food and drug industry

Screening and partial purification of amylase from Aspergillus Niger isolated from deteriorated tomato (Lycopersicon Esculentum mill.) fruits

Amylases (EC 3.2.1.1) are cellwall degrading enzymes associated with the pathogenicity of microorganisms in the spoilage of tomato fruits. The use of amylase in many industries has made it very important to optimize production process to achieve maximum yields. Screening and partial purification of Amylase from Aspergillus niger isolated from tomato (Lycopersicon esculentum Mill.) fruits was studied. Amylase producing fungi were isolated from fresh tomatoes kept at ambient temperature (28±1˚C). Isolates were characterized on the basis of their morphological and cultural techniques. Partial purification of amylase was carried out by ammonium sulphate precipitation. The enzyme activity was determined and optimum conditions were obtained. The molecular weights of the crude and partially purified Amylase were determined by SDS PAGE method. A total of five isolates were obtained using basic screening technique for amylase activity, one of the isolates (Isolate code F2) exhibited maximum amylase activity. The fungi isolate code F2 was identified as Aspergillus niger. Optimum conditions for Amylase AMY F2 were ascertained at pH 6.0; temperature 30°C; substrate concentration of 0.3mg/ml, and time of heating of less than 10min. The molecular weights  f the crude and partially purified Amylase AMY F2 were found to be 55kDa and 35kDa respectively by SDS PAGE method. Microorganisms had been an encouraging means of economical production of enzymes in large scale for the food and drug industry. Keywords: Amylase, Partial Purification, Enzyme, Tomato Fruits Rendement et purification partielle de l'amylase de Aspergillus Niger isolé à partir de tomate déterioré (Lycopersicon Esculentum mill.) fruitsLes amylases (EC 3.2.1.1) sont des enzymes dégradant les parois cellulaires associées à la pathogénicité des microorganismes dans la détérioration des fruits à la tomate. L'utilisation de l'amylase dans de nombreuses industries a rendu très important d'optimiser le processus de production pour obtenir des rendements maximaux. Le dépistage et la purification partielle de l'amylase d'Aspergillus niger isolés à partir des fruits à la tomate (Lycopersicon esculentum Mill.) Ont été étudiés. Les champignons producteurs d'amylase ont été isolés à partir de tomates fraîches conservées à température ambiante (28 ± 1 ° C). Les isolats ont été caractérisés en fonction de leurs techniques morphologiques et culturelles. La purification partielle de l'amylase a été réalisée par précipitation au sulfate d'ammonium. L'activité enzymatique a été déterminée et des conditions optimales ont été obtenues. Les poids moléculaires de l'Amylase brut et partiellement purifiée ont été déterminés par un procédé SDS PAGE. Au total, cinq isolats ont été obtenus en utilisant une technique de dépistage basique pour l'activité amylase, l'un des isolats (code isolé F2) présentait une activité amylase maximale. Le code isolant F2 des Fusions a été identifié comme Aspergillus niger. Les conditions optimales pour Amylase AMY F2 ont été déterminées à pH 6,0; température 30 ° C; concentration de substrat de 0,3 mg / ml et temps de chauffage de moins de 10 min. On a trouvé que les poids moléculaires de l'amylase brute et partiellement purifiée étaient respectivement de 55 kDa et 35 kDa par le procédé SDS PAGE. Les microorganismes ont été un moyen encourageant de production économique d'enzymes à grande échelle pour l'industrie alimentaire et pharmaceutique.Mots-clés: Amylase, Purification partielle, Enzyme, Fruits tomate

Microbiology, heterocyclic amines and polycyclic aromatic hydrocarbons profiles of some grilled, roasted and smoked foods in Lagos and Ogun States, Nigeria

Dietary intake of polycyclic aromatic hydrocarbons (PAH) and heterocyclic amines (HCA) has posted a great health risk as they have been identified as a most potent human carcinogen. Microbial quality of food is also of concern as they contribute to food poisoning and infection. Sixty food samples comprising roasted yam, plantain, grilled and smoked fish and meat were randomly sampled from Lagos and Ogun State, Nigeria, and the PAHs, HCAs contents and microbial load were determined. Isolates were subjected to antibiogram assay. The pH of the samples ranged between 5.08 and 7.49, titrable acidity was in the range of 0.50 and 1.20. Staphylococcus, Bacillus, Micrococcus, Proteus, Pseudomonas, Citrobacter and Klebsiella sp. had been identified. Antibiogram revealed that the isolates were multi-resistant and most resistant to ceftazidime, cloxacillin and tetracycline and more susceptible to ofloxacin. PAHs were detected in some grilled, roasted and smoked samples and with the highest concentrations 314.85 and 139.97 μg/g Dibenzene[a,h]anthracene established in roasted yam and smoked fish samples. Only 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP) was detected in grilled fish and meat samples. This study therefore established the presence of chemical and microbial contaminants in some of the food items investigated. It recommended that strict sanitary practices and appropriate cooking methods be enforced during food preparation

SCREENING AND PARTIAL PURIFICATION OF AMYLASE FROM ASPERGILLUS NIGER ISOLATED FROM DETERIORATED TOMATO (LYCOPERSICON ESCULENTUM MILL.) FRUITS

Amylases (EC 3.2.1.1) are cellwall degrading enzymes associated with the pathogenicity of microorganisms in the spoilage of tomato fruits. The use of amylase in many industries has made it very important to optimize production process to achieve maximum yields. Screening and partial purification of Amylase from Aspergillus niger isolated from tomato (Lycopersicon esculentum Mill.) fruits was studied. Amylase producing fungi were isolated from fresh tomatoes kept at ambient temperature (28±1˚C). Isolates were characterized on the basis of their morphological and cultural techniques. Partial purification of amylase was carried out by ammonium sulphate precipitation. The enzyme activity was determined and optimum conditions were obtained. The molecular weights of the crude and partially purified Amylase were determined by SDS PAGE method. A total of five isolates were obtained using basic screening technique for amylase activity, one of the isolates (Isolate code F2) exhibited maximum amylase activity. The fungi isolate code F2 was identified as Aspergillus niger. Optimum conditions for Amylase AMY F2 were ascertained at pH 6.0; temperature 30°C; substrate concentration of 0.3mg/ml, and time of heating of less than 10min. The molecular weights of the crude and partially purified Amylase AMY F2 were found to be 55kDa and 35kDa respectively by SDS PAGE method. Microorganisms had been an encouraging means of economical production of enzymes in large scale for the food and drug industry

ANTIBACTERIAL ACTIVITY OF MODERATELY VOLATILE COMPONENTS OF THE OIL EXTRACTED FROM THE SEEDS OF DACRYODES EDULIS G. LAM

Objectives: Dacryodes edulis is a versatile plant in many African countries, as its various parts are employed to treat several diseases. Like most plants used in traditional medicine, the possible mechanism by which D. edulis functions is still unknown. This study was designed to investigate the components of the plant seed with a view of justifying its use as traditional medicine. Methods: The seed oil of D. edulis was exhaustively extracted with a Soxhlet extractor from 500 g seeds and 200 g seeds of D. edulis using ethanol and petroleum ether as solvent, respectively. The extraction solvent was removed to obtain the oil which was then subjected to antimicrobial activity test to determine its activity against the following clinical isolates namely Pseudomonas aeruginosa, Staphylococcus aureus, Bacillus cereus, and Escherichia coli using gentamycin as positive control. Phytochemical screening and gas chromatography-mass spectrometry (GC-MS) analyses were carried out following standard methods Results: Ethanolic extract resulted in a higher percentage of oil yield (11.6%) than petroleum ether (5.3%). D. edulis seed oil showed remarkable activity against Gram-negative and Gram-positive isolates: E. coli, Bacillus spp, and S. aureus but not against P. aeruginosa. The presence of saponins, quinones, cardiac glycosides, terpenoids, and phenol was confirmed during qualitative phytochemical screening, and the preliminary results from GC-MS analysis show the presence of terpinen-4-ol, 4,6,6-trimethyl bicyclo[3.1.1]hept-3-en-2-one, ethyl 14-methyl-hexadecanoate, methyl 19-methyleicosanoate, squalene, C-14 to C-18 fatty acids, and their esters. Conclusion: The study, therefore, confirms that the use of D. edulis as component of traditional medicine may be justified

Significance of African Diets in Biotherapeutic Modulation of the Gut Microbiome

Diet plays an essential role in human development and growth, contributing to health and well-being. The socio-economic values, cultural perspectives, and dietary formulation in sub-Saharan Africa can influence gut health and disease prevention. The vast microbial ecosystems in the human gut frequently interrelate to maintain a healthy, well-coordinated cellular and humoral immune signalling to prevent metabolic dysfunction, pathogen dominance, and induction of systemic diseases. The diverse indigenous diets could differentially act as biotherapeutics to modulate microbial abundance and population characteristics. Such modulation could prevent stunted growth, malnutrition, induction of bowel diseases, attenuated immune responses, and mortality, particularly among infants. Understanding the associations between specific indigenous African diets and the predictability of the dynamics of gut bacteria genera promises potential biotherapeutics towards improving the prevention, control, and treatment of microbiome-associated diseases such as cancer, inflammatory bowel disease, obesity, type 2 diabetes, and cardiovascular disease. The dietary influence of many African diets (especially grain-base such as millet, maize, brown rice, sorghum, soya, and tapioca) promotes gut lining integrity, immune tolerance towards the microbiota, and its associated immune and inflammatory responses. A fibre-rich diet is a promising biotherapeutic candidate that could effectively modulate inflammatory mediators’ expression associated with immune cell migration, lymphoid tissue maturation, and signalling pathways. It could also modulate the stimulation of cytokines and chemokines involved in ensuring balance for long-term microbiome programming. The interplay between host and gut microbial digestion is complex; microbes using and competing for dietary and endogenous proteins are often attributable to variances in the comparative abundances of Enterobacteriaceae taxa. Many auto-inducers could initiate the process of quorum sensing and mammalian epinephrine host cell signalling system. It could also downregulate inflammatory signals with microbiota tumour taxa that could trigger colorectal cancer initiation, metabolic type 2 diabetes, and inflammatory bowel diseases. The exploitation of essential biotherapeutic molecules derived from fibre-rich indigenous diet promises food substances for the downregulation of inflammatory signalling that could be harmful to gut microbiota ecological balance and improved immune response modulation

Utilization of nanochitosan in the sterilization of ponds and water treatment for aquaculture

Water pollution constitutes the leading cause of infant mortality, neonatal deformities, and shrinkage of man’s average life expectancy. Pollutants come from point and nonpoint sources; and water pollution arises from the discharge of wastewater containing undesirable impurities used for domestic, agricultural, and industrial purposes. More so, high nutrient and wastewater runoffs from fish production systems contribute to the fouling and eutrophication of recipient water bodies. Hence, aquaculture which is inextricably linked to the natural environment is challenged by the dearth of appropriate water quantity and quality, militating against fish, and fishery production. Nanochitosans as polysaccharides produced by the alkalescent deacetylation of chitin, comprise a series of 2-deoxy-2 (acetylamino) glucose linked by ß-(1-4) glycosidic linkages. They are naturally formed from the deacetylation of shellfish shells and exoskeletons of aquatic arthropods and crustaceans. The unique attributes of chitin confer a wide range of biotechnological applications on the polymer, observed in flocculation as a wastewater treatment and purification route initiated by chitosan. This chapter highlights nanochitosan properties of aquaculture relevance; and elucidates the purification potentials of nanochitosan, compared to inorganic coagulants and organic polymeric flocculants. Effects of chitosan on contaminants and microorganisms, as well as applications in fish pathogens detection, fish disease diagnosis, and control are discussed

Next Generation Nanochitosan Applications in Animal Husbandry, Aquaculture and Food Conservation

Studies have identified the properties of enzymes, functionalized molecules, and compounds in food industry applications as edible coatings and encapsulations, that assure prolonged food quality and standards. These molecules present benefits of longer shelf-life by delayed deterioration and inhibition of the proliferation of spoilage and mycotoxigenic microorganisms. However, challenges of reduced nutrient levels, miniaturized size, and low chemical stability remain concerning. Chitosan polymers naturally formed from the deacetylation of shellfish shells and exoskeletons of aquatic arthropods and crustaceans offer improved benefits when functionalized into nanoparticles as nanochitosans. These polysaccharides produced by the alkalescent deacetylation of chitin, comprise a series of 2-deoxy-2 (acetylamino) glucose linked by ß-(1- 4) glycosidic linkages. This chapter considers the health impacts and microbiological health hazards associated with animal feeds quality and the enzyme immobilization potentials of nanochitosans in animalbased food and feed packages. Thereafter, nanochitosan properties and benefits are compared against traditional preservatives from microbes and plants; with highlights on current challenges in the application of nanochitosan for enzyme immobilization

Chapter 21 - Utilization of nanochitosan in the sterilization of ponds and water treatment for aquaculture

Water pollution constitutes the leading cause of infant mortality, neonatal deformities, and shrinkage of man’s average life expectancy. Pollutants come from point and nonpoint sources; and water pollution arises from the discharge of wastewater containing undesirable impurities used for domestic, agricultural, and industrial purposes. More so, high nutrient and wastewater runoffs from fish production systems contribute to the fouling and eutrophication of recipient water bodies. Hence, aquaculture which is inextricably linked to the natural environment is challenged by the dearth of appropriate water quantity and quality, militating against fish, and fishery production. Nanochitosans as polysaccharides produced by the alkalescent deacetylation of chitin, comprise a series of 2-deoxy-2 (acetylamino) glucose linked by ß-(1-4) glycosidic linkages. They are naturally formed from the deacetylation of shellfish shells and exoskeletons of aquatic arthropods and crustaceans. The unique attributes of chitin confer a wide range of biotechnological applications on the polymer, observed in flocculation as a wastewater treatment and purification route initiated by chitosan. This chapter highlights nanochitosan properties of aquaculture relevance; and elucidates the purification potentials of nanochitosan, compared to inorganic coagulants and organic polymeric flocculants. Effects of chitosan on contaminants and microorganisms, as well as applications in fish pathogens detection, fish disease diagnosis, and control are discussed