Femtosecond time-resolved optical pump-infrared probe spectroscopy was employed to characterize the ethylenic (C=C)-stretch vibrational dynamics (1498-1542 cm(-1)) of the retinal chromophore in Bacteriorhodopsin (BR) during the initial, all-trans to 13-cis isomerization. The early branching reaction was observed, i.e. formation of the ground-state 13-cis product, K, and partial recovery of the all-trans educt state BR570. The BR570 recovery occurs within 2 ps and thus is faster than K-formation (3-4 ps). The IR transients are described in terms of a kinetic model involving vibrational precursors for K and for the recovering BR570, respectively. (C) 1998 Elsevier Science B.V. All rights reserved.