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1.
J Appl Microbiol ; 115(6): 1297-306, 2013 Dec.
Article in English | MEDLINE | ID: mdl-23941529

ABSTRACT

AIMS: The aim of this study was to improve production of pentaene 32,33-didehydroroflamycoin (DDHR) in Streptomyces durmitorensis MS405 strain to obtain quantities sufficient for in depth analysis of antimicrobial properties. METHODS AND RESULTS: Through classical medium optimization conditions for stable growth, DDHR production within 7 days of incubation was established. Yields of 215 mg l(-1) were achieved in shake flask experiments in complex medium with mannitol as the primary carbon source. DDHR had poor antibacterial activity with minimal inhibitory concentrations (MIC) of 400 µg ml(-1) for Staphylococcus aureus and Bacillus subtilis, while MIC of 70 µg ml(-1) was determined for Candida albicans. Using flow cytometry and fluorescent microscopy, it was demonstrated that DDHR induced membrane damage in C. albicans followed by cell death. Combination studies with known antifungal nystatin showed that DDHR is a promising agent for the development of novel antimycotic treatments potentially less toxic for human cells. CONCLUSIONS: Pentaene didehydroroflamycoin has no antibacterial activity but can be further developed for the application in antifungal therapy. SIGNIFICANCE AND IMPACT OF THE STUDY: This study is the first report on the stable and production in high yields of a novel pentaene family that acts on Candida cell membranes and can be used in combination with known antifungals. Polyenes are still antifungal antibiotics of choice, and therefore, isolation and production of new lead structures are highly significant.

2.
J Appl Microbiol ; 113(3): 508-20, 2012 Sep.
Article in English | MEDLINE | ID: mdl-22642403

ABSTRACT

AIMS: The aim of this study was to convert numerous polyaromatic and monoaromatic hydrocarbons into biodegradable polymer medium-chain-length polyhydroxyalkanoate (mcl-PHA). METHODS AND RESULTS: Using naphthalene enrichment cultivation method, we have isolated seven bacterial strains from the river sediment exposed to petrochemical industry effluents. In addition to naphthalene, all seven strains could utilize between 12 and 17 different aromatic substrates, including toluene, benzene and biphenyl. Only one isolate that was identified as Pseudomonas sp. TN301 could accumulate mcl-PHA from naphthalene to 23% of cell dry weight. Owing to poor solubility, a method of supplying highly hydrophobic polyaromatic hydrocarbons to a culture medium was developed. The best biomass and mcl-PHA yields were achieved with the addition of synthetic surfactant Tween 80 (0.5 g l(-1)). We have shown that Pseudomonas sp. TN301 can accumulate mcl-PHA from a wide range of polyaromatic and monoaromatic hydrocarbons, and mixtures thereof, while it could also accumulate polyphosphates and was tolerant to the presence of heavy metal (100 mmol l(-1) cadmium and 20 mmol l(-1) nickel). CONCLUSIONS: A new Pseudomonas strain was isolated and identified with the ability to accumulate mcl-PHA from a variety of aromatic hydrocarbons. SIGNIFICANCE AND IMPACT OF THE STUDY: This study is the first report on the ability of a bacterial strain to convert a range of polyaromatic hydrocarbon compounds to the biodegradable polymer (mcl-PHA). Mcl-PHA is gaining importance as a promising biodegradable thermoelastomer, and therefore, isolation of new producing strains is highly significant. Furthermore, this strain has the ability to utilize a range of hydrocarbons, which often occur as mixtures and could potentially be employed in the recently described efforts to convert waste materials to PHA.


Subject(s)
Hydrocarbons, Aromatic/metabolism , Polyhydroxyalkanoates/biosynthesis , Pseudomonas/metabolism , Biomass , Culture Media/metabolism , Naphthalenes/metabolism , Polyhydroxyalkanoates/isolation & purification , Pseudomonas/isolation & purification
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