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Searching for microorganisms in various, untypical environments is surprisingly effective, therefore the research should be conducted for both conventional plastic and bioplastic.
Extreme microorganisms in various habitats respond to external severe conditions by adapting their physiology through gene expression in order to survive and contain many unique functioning proteins itself.
Recently, with the development of sequencing technologies and the progress of bioinformatics, high throughput sequencing has been broadly applied to study the composition, function, evolution and interaction of microorganisms in various environments.
The ability to predict growth yields on various substrates can be helpful for understanding the growth of microorganisms in various environments as well as for practical applications.
Since anammox bacteria have not been isolated in pure culture, culture-independent methods, specifically DNA/RNA-based molecular techniques, are the most widely used approaches available for detecting this group of microorganisms in various samples (Schmid et al. 2005).
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Polymerase Chain Reaction (PCR) is one of the most widely used molecular methods for detection of a wide variety of microorganism in various clinical samples.
Furthermore, pH is an important factor influencing the growth of a diversity of microorganisms involved in various stages during operation of the process (Chandra et al. 2012).
Microorganisms present in various environments have developed mechanisms of settling on various abiotic and biotic surfaces.
Microorganisms used in various types of biotechnical processes encounter constantly changing environmental conditions, to which they adapt by changing their cellular physiology.
Large numbers of these resident bacteria are present in the digestive tract where they are often in transient, but intimate, contact with exogenous microorganisms that are in various developmental states, including competence.
Concentrations of particular types of microorganisms are commonly measured in various waters, yet the accuracy and precision of reported microorganism concentration values are often questioned due to the imperfect analytical recovery of quantitative microbiological methods and the considerable variation among fully replicated measurements.
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