Well-characterized promoters are essential tools for metabolic engineering and synthetic biology. In Streptomyces coelicolor, the native kasOp is a temporally expressed promoter strictly controlled by two regulators, ScbR and ScbR2. In this work, first, kasOp was engineered to remove a common binding site of ScbR and ScbR2 upstream of its core region, thus generating a stronger promoter, kasOp 3 . Second, another ScbR binding site internal to the kasOp 3 core promoter region was abolished by random mutation and screening of the mutant library to obtain the strongest promoter, kasOp* (where the asterisk is used to distinguish the engineered promoter from the native promoter). The activities of kasOp* were compared with those of two known strong promoters, ermEp* and SF14p, in three Streptomyces species. kasOp* showed the highest activity at the transcription and protein levels in all three hosts. Furthermore, relative to ermEp* and SF14p, kasOp* was shown to confer the highest actinorhodin production level when used to drive the expression of actII-ORF4 in S. coelicolor. Therefore, kasOp* is a simple and well-defined strong promoter useful for gene overexpression in streptomycetes.

High-entropy materials (HEMs), including high-entropy alloys (HEAs), high-entropy oxides (HEOs), and other high-entropy compounds, have gained significant interests over the past years. These materials have unique structures with the coexistence of antisite disordering and crystal periodicity, which were originally investigated as structural materials. Recently, they have emerged for energyrelated applications, such as catalysis, energy storage, etc. In this work, we review the research progress of energy-related applications of HEMs. After an introduction on the background, theory, and syntheses of HEMs, we survey their applications including electrocatalysis, batteries, and others, aiming to retrieve the correlations between their structures and performances. In the end, we discussed the challenges and future directions for developing HEMs.