I want to collect viable probiotic cells (after pH treatment) from a dense soymilk product. This is the protocol i found from a paper to extract DNA from cells:
1) Samples were added with PBS and centrifuge at 700g for 1min to remove debris
2) Supernatant collected and centrifuged at 12,000g for 5mins
3) Pellet collected
My question is does the high speed (12,000g) destroy the cells?
Thanks














