McCain J Scott P, Britten Gregory L, Hackett Sean R, Follows Michael J, Li Gene-Wei
Department of Biology, Massachusetts Institute of Technology, Cambridge, MA, USA.
Department of Earth, Atmospheric and Planetary Sciences, Massachusetts Institute of Technology, Cambridge, MA, USA.
bioRxiv. 2024 Aug 16:2024.08.13.607198. doi: 10.1101/2024.08.13.607198.
Microbes transform their environments using diverse enzymatic reactions. However, it remains challenging to measure microbial reaction rates in natural environments. Despite advances in global quantification of enzyme abundances, the individual relationships between enzyme abundances and their reaction rates have not been systematically examined. Using matched proteomic and reaction rate data from microbial cultures, we show that enzyme abundance is often insufficient to predict its corresponding reaction rate. However, we discovered that global proteomic measurements can be used to make accurate rate predictions of individual reaction rates (median = 0.78). Accurate rate predictions required only a small number of proteins and they did not need explicit prior mechanistic knowledge or environmental context. These results indicate that proteomes are encoders of cellular reaction rates, potentially enabling proteomic measurements to estimate the rates of microbially mediated reactions in natural systems.
微生物通过多样的酶促反应改变其环境。然而,在自然环境中测量微生物反应速率仍然具有挑战性。尽管在全球范围内对酶丰度的量化取得了进展,但酶丰度与其反应速率之间的个体关系尚未得到系统研究。利用来自微生物培养物的匹配蛋白质组学和反应速率数据,我们表明酶丰度往往不足以预测其相应的反应速率。然而,我们发现全球蛋白质组学测量可用于对个体反应速率进行准确的速率预测(中位数 = 0.78)。准确的速率预测仅需要少量蛋白质,且不需要明确的先验机制知识或环境背景。这些结果表明蛋白质组是细胞反应速率的编码器,这可能使蛋白质组学测量能够估计自然系统中微生物介导反应的速率。