Photoelectron emission from solids driven by high intensity lasers offers a platform for the coherent control of electron motion in ultrashort spatiotemporal scales. By solving the time-dependent Schrödinger equation, we present an exact analytical solution for the nonlinear ultrafast electron emission from a dc biased metal surface illuminated by two-color laser fields. We systematically examine the combined effects of a dc electric field and the two-color laser fields. In addition to the remarkable tunability of electron emission processes due to the interference of the two-color laser fields, we find that a strong dc electric field not only opens up more tunneling emission channels, but also introduces intense modulation to the emission current. We found the surprising results that strong current modulation (with respect to the phase difference of the two-color lasers) persists (>70%) even with a large dc bias (i.e. ratio of the electric fields for dc : fundamental laser : second harmonic laser 1 : 0.5 : 0.07). In the meantime, the average emission current level increases by about three orders of magnitude compared to the case of zero dc bias. Application of our model to time-resolved photoelectron spectroscopy is exemplified, showing the dynamics of the n-photon excited states depends strongly on the applied dc field. Our study suggests a practical way to maintain a strong modulation to high current photoemission, by the addition of a large dc bias for two-color laser induced electron emission.