Water-soluble chiral metal clusters have drawn much attention by virtue of their fascinating physicochemical properties and potential biomedical applications, but currently, phosphine-protected Au clusters with both chirality and water-solubility are still very limited. In this article, we demonstrate a mixed-ligand strategy for the facile synthesis of atomically precise, water-soluble chiral Au clusters protected by phosphine alone. The clusters are obtained by the reduction of aurate ions in the presence of a phosphine mixture consisting of highly hydrophilic monophosphine (i.e., triphenylphosphine trisulfonate; TPPTS) and hydrophobic chiral diphosphine (i.e., S-Segphos or S-BINAP), both of which are commercially available. The clusters are size/composition-separated via gel electrophoresis, and notably, heptanuclear cluster Au7(S-Segphos)3(TPPTS)2 exhibits a large chiroptical activity with the maximum anisotropy factor (g-factor) of 4.7 × 10-3, one of the largest values in such Au clusters. Quantum chemical calculations for model Au7 cluster species suggest two important factors to obtain large chiroptical activity: (i) more than two axially-chiral diphosphine ligands, and (ii) the absence of configurational isomer averaging. Consequently, despite the experimental use of a mixture containing both chiral and achiral phosphines, a large chiroptical activity can be created in Au clusters with high water-solubility.