The inclusion of a nuclease, a new‐to‐laundry enzyme class in detergent formulations, reduces the concentration of recalcitrant soils on dirty clothing. Nucleases target extracellular DNA that, albeit present in minor quantities in soiled laundry items, disproportionately contributes to the accumulation of sebaceous soils and other compounds that affect the appearance of clothes. These lingering soils accumulate over multiple wear cycles and provoke a dingy appearance in clothing, characterized by dull colors, yellow staining, and an unpleasant malodor. The single and continued use of a nuclease in detergent formulations offers increased removal of these recalcitrant soils to produce less malodorous and visually preferred textiles. Furthermore, the nuclease is effective across different detergent forms, as well as in cotton short washing cycles, enabling improved cleaning in more sustainable laundry washing conditions.

Washed textiles can remain malodorous and dingy due to the recalcitrance of soils. Recent work has found that ‘invisible’ soils such as microbial extracellular DNA (eDNA) play a key role in the adhesion of extracellular polymeric substances that form matrixes contributing to these undesirable characteristics. Here we report the application of an immunostaining method to illustrate the cleaning mechanism of a nuclease (DNase I) acting upon eDNA. Extending previous work that established a key role for eDNA in anchoring these soil matrixes, this work provides new insights into the presence and effective removal of eDNA deposited on fabrics using high-resolution in-situ imaging. Using a monoclonal antibody specific to Z-DNA, we showed that when fabrics are washed with DNase I, the incidence of microbial eDNA is reduced. As well as a quantitative reduction in microbial eDNA, the deep cleaning benefits of this enzyme are shown using confocal microscopy and imaging analysis of T-shirt fibers. To the best of our knowledge, this is the first time the use of a molecular probe has been leveraged for fabric and homecare-related R&D to visualize eDNA and evaluate its removal from textiles by a new-to-laundry DNase enzyme. The approaches described in the current work also have scope for re-application to identify further cleaning technology.