porosity to support sufficient air exchange. The current clinical approach employed for wound bacterial infection treatment is to apply antibiotics-based wound dressing, which is costly, inefficient, and may lead to antibiotic resistance. [4] Bacterial cellulose (BC), biosynthesized by microorganism fermentation with acetic acid bacteria such as Komagataeibacter sucrofermentans, possesses superior features including high safety, high permeability, high waterholding capacity, excellent flexibility adaptability, low cost, outstanding biocompatibility, and biodegradability. [5] Taking these advantages, BC has been widely applied in artificial skin and blood vessels, scaffolds for tissue engineering, bone regeneration, dental implants, and wound care products. [6] Among these applications, BC is especially suitable for wound dressing because of its 3D coherent nanofiber network structure, leading to ultrahigh porosity and water-holding ability. [6c,7] BC in its natural state does not display any intrinsic antimicrobial capacity, but it can be functionalized with antibacterial agents to realize the infection prevention feature during the wound healing process. [8] Different antibacterial agents such as silver or gold nanoparticles, antibiotics, and chitosan have been attached to BC through physical coating or chemical modification. [9] The physical coating method only requires a moderate modification condition but suffers from shedding of antibacterial moieties from time to time. [10] BC is a natural biopolymer chain composed of β-d-glucose units formed from β-1,4glycosidic bonds. [11] Due to its strong hydrogen bonding and polarizability, BC has poor solubility in conventional organic solvents or water, which often leads to low reaction efficiency for chemical modification. [12] Biosynthesis design for BC by microorganism fermentation has been a new alternative technique that may potentially overcome the limitations of physical coating and chemical modification. [13] Ideally, antibacterial agents could be firmly incorporated into BC during the fermentation process. However, incorporation of an antibacterial agent on BC via microbial biosynthesis is challenging because conventional antibacterial agents could kill the fermentation microorganism. Photosensitizers (PSs), as a class of promising candidates for antibacteria, have no toxicity under dark, but can selectively generate reactive oxygen species (ROS) to induce pathogen lethal injury under light irradiation. [14] Of particular interest are the PSs with aggregationinduced emission characteristics (AIE PSs), which have unique Living materials based on bacterial cellulose (BC) represent a natural and promising candidate for wound dressing. Both physical adsorption and chemical methods have been applied to BC for realizing antibacterial function. However, effective and long-lasting incorporation of bactericidal moieties to BC remains challenging. Herein, a Komagataeibacter sucrofermentans-based direct synthetic method to fabricate photosensitizer-grafted BC thr...