作者: Tsutomu Arakawa , Tiansheng Li , Linda O. Narhi
DOI: 10.1007/978-1-4615-0557-0_2
关键词:
摘要: The production of large quantities proteins became possible with the advent recombinant DNA technology, and subsequent expression in Escherichia coli (E. coli) (Itakura, 1977). Recombinant are produced E. cytoplasm at high concentrations a very different environment than that which they normally expressed. Their structure, stability solubility affected by this can be quite native protein. Therefore, purification often requires techniques those used to purify same protein from its natural environment. Numerous attempts have been made and/or refold expressed proteins.