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Genomic evidence for antibiotic resistance genes of actinomycetes as origins of antibiotic resistance genes in pathogenic bacteria simply because actinomycetes are more ancestral than pathogenic bacteria.

Although in silico analysis have suggested that the antibiotic resistance genes in actinomycetes appear to be the origins of some antibiotic resistance genes, we have shown that recent horizontal transfer of antibiotic resistance genes from actinomycetes to other medically important bacteria have not taken place. Although it has been speculated in Benveniste and Davies' attractive hypothesis that antibiotic resistance genes of actinomycetes are origins of antibiotic resistance genes in pathogenic bacteria because the actinomycetes require mechanisms such as metabolic enzymes (encoded by the antibiotic resistance genes) to degrade the antibiotics they produce or to transport the antibiotics outside the bacterial cells, this hypothesis has never been proven. Both the phylogenetic tree constructed using 16S rRNA gene sequences and that constructed using concatenated amino acid sequences of 15 housekeeping genes extracted from 90 bacterial genomes showed that the actinomycetes is more ancestral to most other bacteria, including the pathogenic Gram-negative bacteria, Gram-positive bacteria, and Chlamydia species. Furthermore, the tetracycline resistance gene of Bifidobacterium longum is more ancestral to those of other pathogenic bacteria and the actinomycetes, which is in line with the ancestral position of B. longum. These suggest that the evolution of antibiotic resistance genes of antibiotic-producing bacteria in general parallels the evolution of the corresponding bacteria. The ancestral position of the antibiotic resistance genes in actinomycetes is probably unrelated to the fact that they produce antibiotics, but simply because actinomycetes are more ancestral than pathogenic bacteria.

Actinobacteria↗

[The investigation on actinomycete population and resources in some areas in Yunnan. IX. The actinomycetes in the west and the northeast of Yunnan].

Two hundred of soil samples of primeval forest, secondary forest, wasteland, nonirrigated farmland, vegetable farmland and paddy farmland were collected from both the west and the northeast of Yunnan in February, 1989. The actinomycetes in the samples were isolated and identified by various methods. This paper discussed the actinomycete population and its difference in the both areas of Yunnan.

Actinomyces↗

Malate dehydrogenases from actinomycetes: structural comparison of Thermoactinomyces enzyme with other actinomycete and Bacillus enzymes.

Malate dehydrogenases from bacteria belonging to the genus Thermoactinomyces are tetrameric, like those from Bacillus spp., and exhibit a high degree of structural homology to Bacillus malate dehydrogenase as judged by immunological cross-reactivity. Malate dehydrogenases from other actinomycetes are dimers and do not cross-react with antibodies to Bacillus malate dehydrogenase.

Bacillus↗

Analysis of actinomycete communities by specific amplification of genes encoding 16S rRNA and gel-electrophoretic separation in denaturing gradients.

A group-specific primer, F243 (positions 226 to 243, Escherichia coli numbering), was developed by comparison of sequences of genes encoding 16S rRNA (16S rDNA) for the detection of actinomycetes in the environment with PCR and temperature or denaturing gradient gel electrophoresis (TGGE or DGGE, respectively). The specificity of the forward primer in combination with different reverse ones was tested with genomic DNA from a variety of bacterial strains. Most actinomycetes investigated could be separated by TGGE and DGGE, with both techniques giving similar results. Two strategies were employed to study natural microbial communities. First, we used the selective amplification of actinomycete sequences (E. coli positions 226 to 528) for direct analysis of the products in denaturing gradients. Second, a nested PCR providing actinomycete-specific fragments (E. coli positions 226 to 1401) was used which served as template for a PCR when conserved primers were used. The products (E. coli positions 968 to 1401) of this indirect approach were then separated by use of gradient gels. Both approaches allowed detection of actinomycete communities in soil. The second strategy allowed the estimation of the relative abundance of actinomycetes within the bacterial community. Mixtures of PCR-derived 16S rDNA fragments were used as model communities consisting of five actinomycetes and five other bacterial species. Actinomycete products were obtained over a 100-fold dilution range of the actinomycete DNA in the model community by specific PCR; detection of the diluted actinomycete DNA was not possible when conserved primers were used. The methods tested for detection were applied to monitor actinomycete community changes in potato rhizosphere and to investigate actinomycete diversity in different soils.

Actinomycetales↗

[Study on diversity of actinomycetes under salt and alkaline environments].

Actinomycetes have been attached a great attention owing to these microorganisms product various natural compounds and have special mechanism of adapting extreme environments. But the research work on actinomycetes under extreme environments is few. Soil and sediment samples were collected from saline and alkaline soil and lakes in Xinjiang, Qinghai Province, P. R. China and Egypt. Diversity and some biological characteristics of Actinomycete were studied by using cultivation and DGGE methods. Results showed that large amount of unknown microorganisms exist in the salt lake Chaka, isolated strains account for only a small portion of species diversity. Designing new strategies for isolation of as yet uncultured microorganisms from natural extreme environments is the key step to exploit microbial resources. The 87% of alkalophilic or alkalinetolerant actinomycete strains were able to grow at pH 6.0 - 12.0. 14 strains grow well at pH 8.5 - 11.5, but not at pH 7.0. 34 halotolerant actinomycete cab grow in 15% - 20% NaCl. Based on the study of the halophilic and halotolerant actinomycetes isolated from the saline and the alkaline soils collected from Xinjiang and Qinghai Province, China, we can conclude that the relationship of actinomycetes (especially halophilic actinomycetes strains) to positive ions such as Na+, K+ and Mg2+ is very complex, and there were sodiumphilic, kaliumphilic, magnesiumphilic, and calciumphilici actinomycete strains. One new family, eight new genera and more than 30 new species of halophilic and alkalophilic actinomycetes were fund. Many strains with PKS genes were selected. We believe based on the research results that there is a very high density of new or unknown actinomycete resources in these areas in China and Egypt.

Actinobacteria↗

Diversity of soil actinomycetes in yunnan, china.

Since 1978, about 4,200 soil samples have been collected from 22 selected areas of various vegetational and climatic types throughout the province of Yunnan. Actinomycetes of 29 genera were isolated by the methods employed. The correlations between diversity and climate were grouped into tropical, subtropical plateau, cool temperate mountain, and snowy mountain types. Actinomycete populations of the first two types were more complex than were the other ones. Correlations between actinomycete diversity and vegetation were also attempted. Six types of vegetation were compared. The diversity of actinomycetes was greatest in soil samples of a primeval forest, with an average of 9.0 genera isolated, followed by secondary forest and vegetable farmland samples, with averages of 6.7 and 6.5 genera isolated, respectively. The upper limit for the occurrence of thermophilic actinomycetes is about 3,500 m above sea level in Yunnan. Psychrophilic actinomycetes were isolated at up to the same altitude. In addition, the drier and poorer the soil was and the cooler the climate was, the lower the count of actinomycetes was and the higher the percentage of streptomycetes observed was. The genus Streptomyces appears to be the most important in ecological function. It represents up to 90% of all soil actinomycete diversity in Yunnan and is likely an important characteristic of the soil actinomycete population.

Journal Article↗