The cortical microtubule array of dark-grown hypocotyl cells of plant seedlings undergoes a striking, and developmentally significant, reorientation on exposure to light. This process is driven by the exponential amplification of a population of longitudinal microtubules, created by severing events localized at crossovers with the microtubules of the pre-existing transverse array. We present a dynamic one-dimensional model for microtubule amplification through this type of templated severing. We focus on the role of the probability of immediate stabilization-after-severing of the newly created lagging microtubule, observed to be a characteristic feature of the reorientation process. Employing stochastic simulations, we show that in the dynamic regime of unbounded microtubule growth, a finite value of this probability is not required for amplification to occur but does strongly influence the degree of amplification and hence the speed of the reorientation process. In contrast, in the regime of bounded microtubule growth, we show that amplification only occurs above a critical threshold. We construct an approximate analytical theory, based on a priori limiting the number of crossover events considered, which allows us to predict the observed critical value of the stabilization-after-severing probability with reasonable accuracy.