Abstract
The review of modern methods of obtaining recombinant enzymes for food industry is given. Optimum condi-tions to obtain recombinant L-phenylalanine-ammonia-lyase Rhodosporidium toruloides allocated from Escherichia coli have been established. The share of the special-purpose protein obtained after the induction was 40 % of the total cell protein. The clearing of the obtained protein on Ni-NTA agarose has been done. The degree of protein clearing was more than 90 %.Keywords
Recombinant strain, enzyme, cloning, genetic engineering, construction, L-phenylalanine-ammonia-lyase, trans-formation, expression vector.REFERENCES
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