Extraction of phospholipid frome minced porcine lung using a combination of Cloroform-Methanol (2:1) and a selected ratio of 1/30 (w/v) between material and solvent showed to be excellent to give in a good yield. Their chemical compositions have been identified and measured comparing with standards, including mainly: phosphatidyl cholin, phosphatidyl serin, phosphatidyl glycerol, and shingomyelin. The purification of product resulted in 80% of total phospholipid.
Surface-Active Agents ; Lung

Aims: This study was aimed to isolate and characterize biosurfactant producing bacteria from Mile 2 and Ologe Lagoon which are sinks for domestic and industrial waste waters and potential source of value added bioresources such as biosurfactants, hydrocarbon degraders and organisms with potential for biotechnological applications. Methodology and results: Physicochemical parameters of the two lagoon waters were analyzed using standard procedures. Bacteria were isolated using enrichment techniques on 1% Escravos light crude oil, palm oil and groundnut oil on mineral salt medium (MSM). Biosurfactant production by the isolates was assayed by hemolytic activity, oil spread test, blue agar test and emulsification activity. Isolates were identified using their colony morphologies and biochemical characteristics, while the antibiotic susceptibility of the isolates was determined using multidisc. The physicochemistry of the lagoon water showed high nitrate content of 15.7 mg/L and 19.6 mg/L for Mile 2 and Ologe Lagoon, respectively. Total hydrocarbon content (THC) of both lagoon waters was low, with values 0.53 mg/L for Mile 2 Lagoon and 0.44 mg/L for Ologe Lagoon. The predominant genera of bacteria identified include Micrococcus, Bacillus, Pseudomonas, Acinetobacter, Stomatococcus and Moraxella. A total of 23 bacterial isolates were tested for hemolytic activity, of which 13 showed β-hemolysis which is presumptive for biosurfactant production, 5 showed α-hemolysis and the remaining 5 exhibited γ-hemolysis. Majority of the isolates were positive for oil spread assay and blue agar test (19) indicating production of anionic biosurfactant. The isolates showed good emulsification activity; AGG3 (67.7%), AGG1 (62.3%), AGG2 (60%), AGG4 (60%), MTP2 (56%), AGC4 (54%) and the least emulsification value of 23.3% for strain AGP1. Most of the isolates were susceptible to ciprofloxacin, perfloxacin and showed resistance to septrin and erythromycin. Conclusion, significance and impact of study This study showed that Mile 2 and Ologe Lagoon are a potential source of biosurfactant producers with diverse emulsification properties and prospective industrial applications. This would have implication for economic empowerment, as well as sustainable and environmentally friendly clean-up technology in both locally and globally.
Surface-Active Agents ; Nigeria

Aims: This study aims to produce Achromobacter biosurfactant in nutrient-rich and nutrient-limited media. Methodology and results: This study conducted fermentation on nutrient-rich and nutrient-limited media using a minimal salt medium (MSM). Dextrose and sodium citrate were used as sole carbon supplemented with 0.5% yeast extract for nutrient-rich media, while nutrient-limited media used molasses and rice straw hydrolysate (RSH) at variations of concentrations of 100 ppm and 200 ppm. The research was performed over 120 h and evaluated from growth response, surface tension and emulsification activity. The study revealed that the best surface tension value was when 2% (w/v) sodium citrate was used as C-source and 0.5% (w/v) yeast extract as N-source, after 72 h upon incubation at 30 °C/120 rpm having 45.45 ± 2.19 mN/m with emulsification activity 24.54 ± 3.42%. Whereas the best result of the nutrient-limited medium was obtained by RSH at a concentration of 200 ppm having 48.86 ± 5.36 mN/m. Conclusion, significance and impact of study The experiment showed that nutrient-limited medium from rice straw hydrolysate could compete with the nutrient-rich medium. The use of rice straw will contribute to the reduction of biosurfactant production costs and valorisation of agricultural waste.
Achromobacter denitrificans ; Surface-Active Agents

The morphological optimization of Trichoderma harzianum was carried out using several surfactants to achieve increased cellulase production. Addition of the surfactants to the culture medium successfully modified the fungal morphology from an aggregated form to a dispersed form. Optimization of the fungal morphology increased cellulase activity up to 177%. The morphologically optimized conditions enhanced the accessibility of the fungus to substrates and thus promoted cellulase production.
Cellulase ; Fungi ; Surface-Active Agents ; Trichoderma*

To effectively solve the serious impact of high oil in the kitchen wastewater on the downstream treatment process, an excellent oil-degrading strain Aeromonas allosaccarophila CY-01 was immobilized to prepare Chitosan-Aeromonas pellets (CH-CY01) by using chitosan as a carrier. Oil degradation condition and efficiency of CH-CY01 pellets were assessed. The growth of immobilized CH-CY01 was almost unaffected, and the maximum degradation rate of soybean oil was 89.7%. Especially at 0.5% NaCl concentration, oil degradation efficiency of CH-CY01 was increased by 20% compared with free cells. In the presence of a surfactant (sodium dodecylbenzene sulfonate) at 1 mg/L, the degradation efficiency of oil by CH-CY01 was increased by 40%. Moreover, using the high-oil catering wastewater as the substrate, more than 80% of the solid oil was degraded with 1% (V/V) CH-CY01 pellets treatment for 7 days, significantly higher than that of free cells. In summary, immobilized CH-CY01 significantly improved the efficiency of oil degradation.
Aeromonas ; Chitosan ; Surface-Active Agents ; Waste Water

Aims: Rhamnolipids are seeking utmost attention as a new class of biosurfactants having promising potential in diverse fields as they offer a wide range of advantages over chemically synthesised surfactants. However, the high extraction costs make large scale production face difficulty. In present study, hydrocarbon degrading bacteria Pseudomonas aeruginosa UKMP14T was exploited for its biosurfactant producing ability including a comparative study between different extraction procedures for its recovery. In addition to this, the recovered biosurfactant was explored for its potential application as an antimicrobial agent. Methodology and results: The production of rhamnolipid biosurfactant was confirmed through various detection methods which are drop-collapse test, oil spreading assay, emulsification index, cetyltrimethylammonium bromide (CTAB) assay and hemolytic assay. The test strain P. aeruginosa UKMP14T showed positive results for all the detection assays. Following this, shake flask cultivation was carried out for several time intervals (1, 3, 5, 7 and 9 days) to discover the optimum time for rhamnolipid biosurfactant production. The results were evaluated by quantifying the rhamnolipid yield using Anthrone method and maximum yield was obtained on day 7. Then, three commonly employed rhamnolipid biosurfactant extraction methods (acid precipitation, solvent extraction and zinc sulphate precipitation) were incorporated for the extraction of rhamnolipid biosurfactant. Among these methods, organic solvent extraction (using methanol, chloroform and acetone in 1:1:1 ratio) gave the highest yield (7.37 ± 0.81 g/L) of biosurfactant, followed by zinc sulphate precipitation (5.83 ± 0.02 g/L), whereas acid precipitation gave the lowest yield (2.8 ± 0.12 g/L) and required longer time (30 days). Finally, the antimicrobial activity of several concentrations of rhamnolipid was tested using modified microdilution method and highest antibacterial activity (in the form of percent reduction in growth) of 95.05% and 91.89% was recorded for Escherichia coli ATCC 10536 and Staphylococcus aureus ATCC 11632, respectively, at 100 µg/mL concentration of rhamnolipid biosurfactant. Conclusion, significance and impact of study The ability of P. aeruginosa UKMP14T in producing rhamnolipid biosurfactant was confirmed. Despite the higher yield obtained by organic solvent extraction method, the recovery technique (involving the separation of solvent system) caused some loss in product. In addition, the transfer and storage of rhamnolipid was challenging using solvent extraction in comparison to acid precipitation and zinc sulphate precipitation. On the other hand, recovery using acid precipitation suffered from lowest yield of rhamnolipid. Therefore, zinc sulphate precipitation is prioritised over the other two methods. Furthermore, the antimicrobial potential of rhamnolipid biosurfactant was tested successfully for as low as 10 µg/mL concentration against E. coli ATCC 10536 and S. aureus ATCC 11632. Therefore, the recovery cost of a high value product like rhamnolipid can be reduced by incorporating the results of this study in the downstream processing and promote rhamnolipid biosurfactant as a potential antimicrobial agent.
Glycolipids--biosynthesis ; Surface-Active Agents ; Pseudomonas aeruginosa

Aims: This study was aimed to investigate the anti-inflammatory and anti-rheumatoid effects of the Bacillus amyloliquefaciens derived surfactin. Methodology and results: Crude and biosurfactant extracts were analyzed using thin-layer chromatography to determine the presence of biosurfactant. Both extracts were evaluated for their inhibitory effects against the acetylcholinesterase and 5-lipoxygenase enzymes. Human synovial cells were induced with TNF-α and IL-1β. The percentages of the cell viability for both normal and induced cells were determined with an MTT assay. Results showed that surfactin was detected in the biosurfactant extract and demonstrated higher inhibitory effects compared to the crude extract against both inhibitory enzymes acetylcholinesterse (IC50=30.60 μg/mL) and lipoxygenase (IC50=110.10 μg/mL). Both crudes showed no cytotoxic effects at the highest concentration used (50 μg/mL) against normal human synovial cells but showed active reactions against the induced cells. The anti-proliferative effects of biosurfactant and crude extracts were in dose-dependent manner. Conclusion, significance and impact of study Notably, surfactin obtained from B. amyloliquefaciens has shown an inhibitory effect against pro-inflammatory enzymes and cell viability of the induced rheumatoid arthritis cell line. These results highlighted the therapeutic potential of surfactin application as an anti-inflammatory agent for arthritis treatment. Further study is needed to elucidate the mechanisms underlying the anti-inflammatory effect of surfactin.
Bacillus amyloliquefaciens ; Surface-Active Agents ; Anti-Inflammatory Agents ; Rheumatoid Factor

An experimental study concerning the effect of chronic irritation of corneocytes was made in relation to their number, size and shape. The desquamating portion of the stratum corneum was sampled with the detergent scrub technique using Triton X-100. The experimental subjects were scrub nurses who had worked in the operating room for more than 3 years and ward nurses were used as a control group. The corneocytes of skin irritated by daily scrubbing differed, from those of the non-irritated skin of the ward nurses. About twice as many cells were collected per cm2 skin surface from the scrub nurses on the first experimental day. Two and four days later the number was markedly decreased and became similar to that of the control group. The surface of the corneocytes was 15% smaller in the experimental group than that of the control group, through out the experiment. There was no significant difference between the two groups as regards corneocyte morphology.
Adult ; Epidermis/cytology* ; Female ; Handwashing* ; Human ; Soaps* ; Surface-Active Agents*

OBJECTIVETo provide better laboratory protection material in virology lab to prevent laboratory accident infection.

METHODSThe four kinds of ionic polypropylene fibers were constructed and interact with recombinant adenovirus expressing GFP. Both the GFP expression and hexon gene expression of recombiant adenovirus were used to evaluate absorb ability of fibers.

RESULTSBoth the amphoteric and iron ionic polypropylene fibers have certain adsorption or inactivated ability to virus in 5 min, the other two fibers decreased the growth within 20 min.

CONCLUSIONBoth the amphoteric and iron ionic polypropylene fibers can be used as laboratory protection material in virology lab.

No abstract available.
Humans ; Infant, Newborn ; Infant, Premature ; Surface-Active Agents