Mutagenesis breeding of high echinocandin B producing strain and further titer improvement with culture medium optimization
Bioprocess and Biosystems Engineering, ISSN: 1615-7605, Vol: 38, Issue: 10, Page: 1845-54
2015
- 23Citations
- 21Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations23
- Citation Indexes23
- 23
- CrossRef5
- Captures21
- Readers21
- 21
Article Description
A combination of microbial strain improvement and statistical optimization is investigated to maximize echinocandin B (ECB) production from Aspergillus nidulans ZJB-0817. A classical sequential mutagenesis was studied first by using physical (ultraviolet irradiation at 254 nm) and chemical mutagens (lithium chloride and sodium nitrite). Mutant strain ULN-59 exhibited 2.1-fold increase in ECB production to 1583.1 ± 40.9 mg/L when compared with the parent strain (750.8 ± 32.0 mg/L). This is the first report where mutagenesis is applied in Aspergillus to improve ECB production. Further, fractional factorial design and central composite design were adopted to optimize the culture medium for increasing ECB production by the mutant ULN-59. Results indicated that four culture media including peptone, KHPO, mannitol and l-ornithine had significant effects on ECB production. The optimized medium provided another 1.4-fold increase in final ECB concentration to 2285.6 ± 35.6 mg/L compared to the original medium. The results of this study indicated the combined application of a classical mutation and medium optimization can improve effectively ECB production from A. nidulans and could be a promising tool to improve other secondary metabolites production by fungal strains.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85027957121&origin=inward; http://dx.doi.org/10.1007/s00449-015-1425-4; http://www.ncbi.nlm.nih.gov/pubmed/26091897; http://link.springer.com/10.1007/s00449-015-1425-4; https://dx.doi.org/10.1007/s00449-015-1425-4; https://link.springer.com/article/10.1007%2Fs00449-015-1425-4
Springer Science and Business Media LLC
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