User:YahKaeru/Bacillus subtilis

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[1]While the natural competent state is common within laboratory B. subtilis and field isolates, some industrially relevant strains, e.g. B. subtilis (natto), are reluctant to DNA uptake due to the presence of restriction modification systems that degrade exogenous DNA. B. subtilis (natto) mutants, which are defective in a type I restriction modification system endonuclease, are able to act as recipients of conjugative plasmids in mating experiments, paving the way for further genetic engineering of this particular B. subtilis strain.[2].

By adopting Green Chemistry in the use of less hazardous materials, while saving cost, researchers have been mimicking nature's methods of synthesizing chemicals that can be useful for the food and drug industry, by "piggybacking molecules on shorts strands of DNA" before they are zipped together during their complimentary base pairing between the two strands. Each strand will carry a particular molecule of interest that will undergo a specific chemical reaction simultaneously when the two corresponding strands of DNA pairs hold together like a zipper, allowing another molecule of interest, to react with one another in controlled and isolated reaction between those molecules being carried into these DNA complimentary attachments. By using this method with certain bacterias that naturally follow a process replication in a multi-step fashion, the researchers can simultaneously carry on the interactions of these added molecules to interact with enzymes and other molecules used for a secondary reaction by treating it like a capsule, which is similar to how the bacteria performs it's own DNA replication processes.

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  1. ^ "Chemistry AU naturel: mimicking nature's clean and efficient ways. - Free Online Library". www.thefreelibrary.com. Retrieved 2023-04-29.
  2. ^ Itaya M, Nagasaku M, Shimada T, Ohtani N, Shiwa Y, Yoshikawa H, et al. (February 2019). "Stable and efficient delivery of DNA to Bacillus subtilis (natto) using pLS20 conjugational transfer plasmids". FEMS Microbiology Letters. 366 (4). doi:10.1093/femsle/fnz032. PMID 30726909.