Biofilm Formation by Marine Cobetia marina alex and Pseudoalteromonas spp: Development and Detection of Quorum Sensing N-Acyl Homoserine Lactones (AHLs) Molecules

Surfaces submerged in seawater are colonized by various microorganisms, resulting in the formation of heterogenic marine biofilms. This work aims to evaluate the biofilm formation by Cobetia marina alex and doing a comparative study between this promising strain with the two bacterial strains isolated previously from the Mediterranean seawater, Alexandria, Egypt. Three strains; Cobetia marina alex, Pseudoalteromonas sp. alex, and Pseudoalteromonas prydzensis alex were screened for biofilm formation using the crystal violet (CV) quantification method in a single culture. The values of biofilm formed were OD600= 3.0, 2.7, and 2.6, respectively leading to their selection for further evaluation. However, factors affecting biofilm formation by C. marina alex were investigated. Biofilm formation was evaluated in single and multispecies consortia. Synergistic and antagonistic interactions proved in this work lead to the belief that these bacteria have the capability to produce some interesting signal molecules N-acyl Homoserine Lactones (AHLs

Characterization of Biofilm Forming Marine Pseudoalteromonas spp

Biofilm forming bacteria are omnipresent in the marine environment. Pseudoalteromonas is one of the largest within the γ-proteobacteria class, and a member of marine bacteria. Species of Pseudoalteromonas are generally found in association with marine eukaryotes. In this work, we present the isolation and characterization of two strains forming biofilm on rock surface and associated with marine sponge. They were identified using 16SrDNA as Pseudoalteromonas prydzensis alex, and Pseudoalteromonas sp. alex. They showed the highest titer in biofilm formation quantified using the test tube method using crystal violet

Agarase Production by Marine Pseudoalteromonas sp. MHS: Optimization, and Purification

Agar is an essential polysaccharide that has been utilized in numerous fields. Many kinds of literature have been published regarding agarolytic microorganisms’ isolation and agarases biochemical studies. In this search, a local marine agarolytic bacterium associated with marine alga Ulva lactuca surface was isolated and identified as Pseudoalteromonas sp. MHS. The agarase production was parallel to the growth of Pseudoalteromonas sp. MHS as cells displayed a lag phase (2 h), subsequently an exponential growth that prolonged till 10 h where maximum growth (OD550nm = 3.9) was achieved. The enzyme activity increased rapidly as cells increased exponentially where the maximum activity of 0.22 U/mL was achieved after 8h and remained constant till 12 h during the stationary phase of growth. Agarase production was optimized using Plackett-Burman statistical design by measuring enzyme activity as a response and the design was validated using a verification experiment; the activity of the enzyme increased from 0.22 U/mL to 0.29 U/mL. Pseudoalteromonas sp. MHS agarase was partially purified and its molecular weight (MW) was determined by SDSPAGE (15-25 kDa). Agarase showed approximately 94% of its activity at 40 °C. The enzyme stability decreased as the temperature increased; the enzyme could retain about 98, 90, 80, 75, and 60% of its activity at 20, 30, 40, 50, and 60 °C, respectively. Biomass of the red alga Pterocladia capillacea proved to be a suitable substrate for agarase production using Pseudoalteromonas sp. MHS; the enzyme activity recorded after 24 h of incubation was 0.35 U/mL compared to 0.29 U/mL from the optimized medium

Potential Egyptian bacterial consortium for oil spill treatment: A laboratory simulation

The purpose of the study was to reach high efficiency of an oil-degrading bacteria to be used in oil-spill treatment separately or with bacterial consortium. The consortium effect on crude oil was examined by GC-MS. The consortium degraded 99.2% of crude oil after 7 days, while Enterobacter sp. ASH, as individual culture, degraded 80% only. This isolate was identified based on 16S rRNA gene sequence analysis, morphological, physiological, and biochemical characterization. ANOVA analysis showed that medium volume and crude oil concentration are the significant factors. The results showed that the mixed consortium showed better biodegradation abilities than E. sp. ASH