High-intensity green light potentially activates the actinorhodin biosynthetic pathway in Streptomyces coelicolor A3(2).

The development of practices that enhance the potential of actinomycetes as major antibiotic producers is a challenge in discovering new secondary metabolites. Light, an essential external stimulus for most microorganisms, could be exploited to manipulate their physiological processes. However, the effects of monochromatic green light on the production of secondary metabolites in actinomycetes have not yet been reported. In this paper, we report a novel and simple method that uses high-intensity monochromatic green light to potentially induce the production of cryptic secondary metabolites in the model actinomycete Streptomyces coelicolor A3(2). Using actinorhodin (ACT), a blue-pigmented antibiotic, and undecylprodigiosin (RED), a red-pigmented antibiotic, as indicators, we found that irradiation with high-intensity monochromatic green light-emitting diodes promoted sporulation, significantly decreased RED production, and increased ACT production. Semi-quantitative reverse transcription-polymerase chain reaction and western blot analyses revealed, for the first time, that stimulation with green light accelerated the expression of ActII-ORF4, a pathway-specific regulator of ACT biosynthesis in S. coelicolor A3(2). This approach of stimulating secondary metabolite biosynthesis pathways in actinomycetes by irradiation with high-intensity monochromatic green light is expected to facilitate the discovery of cryptic antibiotics that are not typically produced under conventional dark culture conditions. However, the effective intensity and duration of irradiation with green light that are required to activate these metabolite pathways may vary markedly among actinomycetes.

Streptomyces Diversity Maps Reveal Distinct High-Specificity Biogeographical and Environmental Patterns Compared to the Overall Bacterial Diversity.

Despite their enormous impact on the environment and humans, the distribution and variety of the biggest natural secondary metabolite producers, the genus Streptomyces, have not been adequately investigated. We developed representative maps from public EMP 16S rRNA amplicon sequences microbiomics data. Streptomyces ASVs were extracted from the EMP overall bacterial community, demonstrating Streptomyces diversity and identifying crucial diversity patterns. Our findings revealed that while the EMP primarily distinguished bacterial communities as host-associated or free-living (EMPO level 1), the Streptomyces community showed no significant difference but exhibited distinctions between categories in EMPO level 2 (animal, plant, non-saline, and saline). Multiple linear regression analysis demonstrated that pH, temperature, and salinity significantly predicted Streptomyces richness, with richness decreasing as these factors increased. However, latitude and longitude do not predict Streptomyces richness. Our Streptomyces maps revealed that additional samplings in Africa and Southeast Asia are needed. Additionally, our findings indicated that a greater number of samples did not always result in greater Streptomyces richness; future surveys may not necessitate extensive sampling from a single location. Broader sampling, rather than local/regional sampling, may be more critical in answering microbial biogeograph questions. Lastly, using 16S rRNA gene sequencing data has some limitations, which should be interpreted cautiously.

Fusigen Reduces Intracellular Reactive Oxygen Species and Nitric Oxide Levels.

BACKGROUND/AIM: Oxidative stress caused by the production of excessive cellular reactive oxygen species (ROS) and high levels of nitric oxide contribute to several human pathologies. This study aimed to examine the anti-oxidant effects of fusigen, a compound produced from Aureobasidium melanogenum. MATERIALS AND METHODS: Extracts of A. melanogenum were selected as a source for the isolation of fusigen. The anti-oxidant, nitric oxide suppression, as well as the free radical scavenging activities of fusigen were tested in BEAS-2B human bronchial epithelial cell line (BEAS-2B cells) and human dermal papilla cells (DP cells) using specific fluorescence dyes and flow cytometry analysis. Cell viability was determined by the MTT assay. RESULTS: Fusigen did not exert cytotoxicity in the human normal BEAS-2B and DP cells at concentrations up to 100 µM. Fusigen decreased basal levels of cellular ROS, as well as the levels of ROS induced by hydrogen peroxide and ferrous ion enrichment. ROS decreasing effect was confirmed in DP cells. In addition, fusigen treatment suppressed intracellular NO levels in both BEAS-2B and DP cells. CONCLUSION: The optimal process of production of purified fusigen from A. melanogenum was determined. Fusigen exhibited a low cytotoxic effect and the potential to suppress ROS and NO. These results demonstrated that fusigen may be used for the treatment or prevention of human diseases.