Sentence examples for microbial producer from inspiring English sources

We here apply Metabolic engineering to Guide Evolution (MGE), an evolutionary approach evolving and identifying new targets to improve microbial producer strains.

Combination with concurrently developing improvements in important accessory technologies such as DNA synthesis, high-throughput screening methods, regulatory element design, and metabolic pathway optimization tools has resulted in novel efficient microbial producer strains and given access to new metabolic products.

The generation of microbial producer strains for the sustainable and economically feasible production of biofuels through photosynthetic processes is considered a challenging topic of research.

For identification of the bioactive compounds in microbial products extracts, bioassay-guided fractionation and further purification of the active molecule from new, large-scale refermentation of the original microbial producer are required.

Depending on the microbial producer and the applied purification method, RSD amylases could be purified by 2.8- or 8.5-fold at 12 or 60.5 % yield from Aspergillus sp. (Okolo et al. 2001), 6-fold at 38%% yield from Bacillus licheniformis (Božić et al. 2011), 5.4-fold at 72.9 % yield from Rhizopus sp. (Morita et al. 1998), or by 34-fold at 6.6 % yield from Bacillus sp. (Liu and Xu 2008).

Several genetic engineering strategies have been employed to produce 1,3-PDO in both native and non-native microbial producers (reviewed in [ 10]).

Microbial producers such as Escherichia coli are evolutionarily trained to adapt to changing substrate availabilities.

In this work, an overview of the bioprocesses developed for EPS production by the wide diversity of reported microbial producers is presented, including their development and scale-up.

The presence of both pentose and hexose sugars in the fermentation broth, the price of cellulolytic enzymes, and the presence of toxic compounds that can inhibit cellulolytic enzymes and microbial producers of ethanol are major issues.

In the case of β-amyrin formation the triple over-expression construct exhibited a nearly 500% increase over the control strain making our metabolic engineering strategy the most successful design of triterpene microbial producers.

Thus, many companies have turned the search for microbial producers of novel antifungal compounds to other environments such as hydrothermal vents, marine environments, tropical rain forests, and microbial symbionts associated with plants and animals hosts [ 5, 6].