柠檬酸循环
磷酸烯醇丙酮酸羧激酶
同位素
焊剂(冶金)
细菌
柠檬酸合酶
生物化学
生物
新陈代谢
化学
酶
分子
遗传学
有机化学
作者
Hui Li,Tian-tuo Zhang,Zhuang‐Gui Chen,Jin-zhou Ye,Song Zhang,Jun Yang,Xuan‐xian Peng,Bo Peng
标识
DOI:10.1073/pnas.1812316115
摘要
Nikaido (1) claims, contrary to our work (2), that the P cycle is not a general mechanism for energy production and that it does not sensitize bacteria toward aminoglycosides. However, the argumentation for both points is not convincing to us.
The P cycle is proposed from the stable-isotope–based nontargeted isotope fate detection analysis, in which we found labeled glutamate flux to glucogenesis and identified three additional steps—transforming oxaloacetate (OAA) to citrate through phosphoenolpyruvate (PEP), pyruvate, and acetyl-CoA—to finish the metabolic process. The finding was further supported by 13C-labeled glucose in figure 7G of ref. 2. The PEP-pyruvate-OAA node, also referred to as the anaplerotic node, is a main way …
[↵][1]1To whom correspondence may be addressed. Email: pengb26{at}sysu.edu.cn or pxuanx{at}sysu.edu.cn.
[1]: #xref-corresp-1-1
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