lucaspa
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DrLao said:Any idea what this previously 472 residue-long arginine-rich protein did? Was it involved in carboydrate hydrolysis?
And how could they tell whether 6-aminohexanoic acid linear oligomer hydrolase had any activity on non-nylon substrates if the bacteria could effectively use those substrates with other enzymes?
Second one first: you purify the enzyme and test it on the substrates. This is standard procedure to determine the substrate of any enzyme.
It turns out that the original sequence seems to have been NON-coding. IOW, later work showed that the sequence was not translated to a protein. Thomas needs to update the website.
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