This should be re-titled something like: with 200x longer sequences and making products without culturing, dirt can make antibiotic gold. The two prospects: Erutacidin, disrupts bacterial membranes through an uncommon interaction with the lipid cardiolipin and is effective against even the most challenging drug-resistant bacteria. trigintamicin, acts on a protein-unfolding motor known as ClpX, a rare antibacterial ta…
> So being able to make the product without culturing the organism is key.
No, it isn't. The article talks about using chemical synthesis, rather than using a biological platform to express the product via genes.
"To convert the newly uncovered sequences into bioactive molecules, the team applied a synthetic bioinformatic natural products (synBNP) approach. They bioinformatically predicted the chemical structures of natural products directly from the genome data and then chemically synthesized them in the lab. With the synBNP approach, Brady and colleagues managed to turn the genetic blueprints from uncultured bacteria into actual molecules—including two potent antibiotics."