Background: The bacteria Aeromonas hydrophila was isolated from clinical specimens responsible of causing diarrhea in children and adults. Objective:To purify metalloprotease enzyme produced by Aeromonas hydrophila. Patients and Methods: This study involved 150 stool samples collected from patients suffering from diarrhea. Results: Eight isolate of Aeromonas hydrophila was detected and metalloprotease was purified with 11.06 U/ml of enzyme activity. Conclusion: The bacteria have ability to produce metalloprotease and enzyme was fully purified in three steps of purification.

The isolates of Staphylococcus aureus were isolated from patients with various infections in hospitals, the isolates were identified and accurately diagnosed by phenotypic examination and biochemical tests, as well Vitek-2, and then genetic detection and diagnosis of many of the pathogenic factors associated with Staphylococcus aureus using conventional polymerase chain reaction (PCR) and testing for association by antibiotic resistance and production of some toxins by Staphylococcus aureus. After performing analysis of statistical, it was set up that the correlation coefficient of the PCR technique using virulence genes, sensitivity test to antibiotics and other virulence factors were significant at p < 0.05, but was insignificant with the biofilm production.

One hundred and fifty stool sampling were collected from clinical sources responsible of causing diarrhea in adults as well as children. The identification of Aeromonas hydrophila isolates depended on common methods of identification dependent on biochemical characteristics and culture, then vitek2 compact system was used. Eight Aeromonas hydrophila isolates were gained and revealed various productivity of metalloprotease; the isolate number 8 was the maximum effective in metalloprotease production. The eight isolates were examined with Polymerase Chain Reaction to prove enzyme gene presence, the results revealed that all isolates were positive for ahMP genes; metalloprotease was completely purified via a number of steps, which included ammonium sulphate precipitation, dialysis, ion exchange and gel chromatography. Cytotoxicity effect of metalloprotease studies on cancer and normal cell lines, The results showed the purified metalloprotease as effective cytotoxic effect on liver hepatocellular cancer cells (HepG2) compared with no effect on normal liver cell line (WRL-68) indicating less cytotoxic effect.

Twenty fresh clover honey, ten beeswax and ten bee bread samples represented contaminated and non-contaminated areas were collected directly from the apiaries during 2015 .The aim of this study was to evaluate the presence of toxic metals ( Lead (Pb), Cadmium (Cd), Iron (Fe), Copper (Cu) and Zinc (Zn)) in honey, beeswax and bee bread stored inside honey bee colonies. The highest lead contents (0.5488 mg/kg) was estimated in honey samples collected from industrialized area The lowest Pb content were estimated in honey samples collected from rural area (0.5096 mg/kg).The lowest Cd concentration (0.0961 mg/kg). However, the highest content of Cd (0.1042 mg/kg) was recorded in honey samples collected from urbanized areas. High concentration of (Cu) was estimated in honey samples collected from apiaries located in industrialized area (0.0757 mg/kg) while the lowest were recorded in rural area (0.0432 mg/kg) . Zn occurred in low concentration in honey samples The highest value was recorded in honey samples from rural area (0.241) mg/kg and the lowest in honey samples from apiaries located in Reclaimed soils (0.185) mg/kg. Heavy metalconcentrations of Pb, Cd, Fe, Cu and Zn in beeswax samples collected from contaminated and non-contaminated areas were 1.388, 0.194, 16.696, 0.619 and 4.606 mg/kg. While the averages of heavy metal concentrations in non contaminated area decreased to 1.175; 0.160; 15.466; 0.391 and 2.520 mg/kg, respectively. Contamination in bee bread samples showed that lead concentration (1.094 mg/kg to 1.338 mg/kg) was detected in bee bread samples collected from honey bee colonies located in non-contaminated areas and samples collected from( industrialized and urban areas).