Possot O M, Gérard-Vincent M, Pugsley A P
Unité de Génétique Moléculaire, CNRS URA1773, Institut Pasteur, 75724 Paris Cedex 15, France.
J Bacteriol. 1999 Jul;181(13):4004-11. doi: 10.1128/JB.181.13.4004-4011.1999.
The PulC component of the Klebsiella oxytoca pullulanase secretion machinery (the secreton) was found by subcellular fractionation to be associated with both the cytoplasmic (inner) and outer membranes. Association with the outer membrane was independent of other secreton components, including the outer membrane protein PulD (secretin). The association of PulC with the inner membrane is mediated by the signal anchor sequence located close to its N terminus. These results suggest that PulC forms a bridge between the two membranes that is disrupted when bacteria are broken open for fractionation. Neither the signal anchor sequence nor the cytoplasmic N-terminal region that precedes it was found to be required for PulC function, indicating that PulC does not undergo sequence-specific interactions with other cytoplasmic membrane proteins. Cross-linking of whole cells resulted in the formation of a ca. 110-kDa band that reacted with PulC-specific serum and whose detection depended on the presence of PulD. However, antibodies against PulD failed to react with this band, suggesting that it could be a homo-PulC trimer whose formation requires PulD. The data are discussed in terms of the possible role of PulC in energy transduction for exoprotein secretion.
通过亚细胞分级分离发现,产酸克雷伯菌普鲁兰酶分泌机制(分泌装置)的PulC组分与细胞质(内膜)和外膜均有关联。与外膜的关联独立于其他分泌装置组分,包括外膜蛋白PulD(分泌素)。PulC与内膜的关联由靠近其N端的信号锚定序列介导。这些结果表明,PulC在两个膜之间形成了一座桥梁,当细菌被破碎用于分级分离时这座桥梁会被破坏。未发现PulC功能需要信号锚定序列或其前面的细胞质N端区域,这表明PulC不会与其他细胞质膜蛋白发生序列特异性相互作用。对完整细胞进行交联导致形成了一条约110 kDa的条带,该条带与PulC特异性血清发生反应,其检测依赖于PulD的存在。然而,针对PulD的抗体未能与这条带发生反应,这表明它可能是一个同型PulC三聚体,其形成需要PulD。本文根据PulC在外蛋白分泌的能量转导中的可能作用对数据进行了讨论。