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With the development of metabolic engineering and synthetic biology, many microorganisms have been designed and modified for obtaining desired phenotypes.
Many microorganisms have the innate capability to discharge and/or receive electrons to and from solid state materials such as electrodes.
Although many microorganisms have been used for the bioindustrial generation of valuable metabolites, the productive potential of cyanobacterial species has remained largely unexplored.
Many microorganisms have been identified as causative agents for ICK.
Bactericidal effects that the TiO2/UV process has on many microorganisms have been confirmed.
In the past decades, many microorganisms have been isolated and investigated for use as a biocontrol agent.
Similar(41)
Furthermore, genome mining has expanded the definition of exactly what constitutes a secondary metabolite producer and has revealed that the biosynthetic potential of many microorganisms has been widely underestimated [ 7– 9].
It is extensively used in the food and fermentation industry such as for saccharification of starch, brewing, production of high-fructose syrup, etc. Aspergillus niger, Aspergillus awamori, and Rhizopus oryzae are the commonly used filamentous fungi for the industrial production of GA, though many other microorganisms have also been explored for the same.
Many antagonistic microorganisms have been proved to be active In vitro or in vivo.
Although many oleaginous microorganisms have been intensively investigated to produce microbial oils (Papanikolaou and Aggelis 2011; Ratledge and Wynn 2002), the regulatory mechanism of lipid biosynthesis in these organisms, especially the role of lysine acetylation in the regulation of these processes, is largely unknown.
Many biodetoxification microorganisms have been discovered and the biodetoxification mechanisms were extensively investigated [ 14– 17].
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