“…These and other common mechanisms of resistance to AMPs are highlighted in Figure 6. [75] costs, rapid growth on inexpensive substrates, controllable laboratory conditions, and the generally well-characterized genetic backgrounds and availability of a wide range of vectors and host strains [93]. The use of fusion proteins is common in the production of small, labile AMPs to provide stabilization, shield the AMP from intracellular proteolytic degradation, increase expression and facilitate downstream purification processes, but more importantly to mask the intrinsic toxicity of these peptides to the expression host [91,94,95].…”