Zhou Guangyin, Kowalczyk David, Humbard Matthew A, Rohatgi Sunil, Maupin-Furlow Julie A
Department of Microbiology and Cell Science, University of Florida, Gainesville, FL 32611-0700, USA.
J Bacteriol. 2008 Dec;190(24):8096-105. doi: 10.1128/JB.01180-08. Epub 2008 Oct 17.
Little is known regarding the biological roles of archaeal proteases. The haloarchaeon Haloferax volcanii is an ideal model for understanding these enzymes, as it is one of few archaea with an established genetic system. In this report, a series of H. volcanii mutant strains with markerless and/or conditional knockouts in each known proteasome gene was systematically generated and characterized. This included single and double knockouts of genes encoding the 20S core alpha1 (psmA), beta (psmB), and alpha2 (psmC) subunits as well as genes (panA and panB) encoding proteasome-activating nucleotidase (PAN) proteins closely related to the regulatory particle triple-A ATPases (Rpt) of eukaryotic 26S proteasomes. Our results demonstrate that 20S proteasomes are required for growth. Although synthesis of 20S proteasomes containing either alpha1 or alpha2 could be separately abolished via gene knockout with little to no impact on growth, conditional depletion of either beta alone or alpha1 and alpha2 together rendered the cells inviable. In contrast, the PAN proteins were not essential based on the robust growth of the panA panB double knockout strain. Deletion of genes encoding either alpha1 or PanA did, however, render cells more sensitive to growth on organic versus inorganic nitrogen sources and hypo-osmotic stress and limited growth in the presence of l-canavanine. Abolishment of alpha1 synthesis also had a severe impact on the ability of cells to withstand thermal stress. This contrasted with what was seen for panA knockouts, which displayed enhanced thermotolerance. Together, these results provide new and important insight into the biological role of proteasomes in archaea.
关于古菌蛋白酶的生物学作用,人们了解甚少。嗜盐古菌沃氏嗜盐菌是理解这些酶的理想模型,因为它是少数具有成熟遗传系统的古菌之一。在本报告中,系统地构建并表征了一系列在每个已知蛋白酶体基因中无标记和/或条件性敲除的沃氏嗜盐菌突变株。这包括编码20S核心α1(psmA)、β(psmB)和α2(psmC)亚基的基因以及编码与真核生物26S蛋白酶体的调节颗粒三磷酸腺苷酶(Rpt)密切相关的蛋白酶体激活核苷酸酶(PAN)蛋白的基因(panA和panB)的单敲除和双敲除。我们的结果表明,生长需要20S蛋白酶体。虽然通过基因敲除可以分别消除含有α1或α2的20S蛋白酶体的合成,对生长几乎没有影响,但单独条件性耗尽β或同时耗尽α1和α2会使细胞无法存活。相比之下,基于panA panB双敲除菌株的强劲生长,PAN蛋白并非必需。然而,删除编码α1或PanA的基因确实使细胞在有机氮源与无机氮源上生长以及在低渗胁迫下对生长更敏感,并且在存在L-刀豆氨酸的情况下生长受限。α1合成的消除也对细胞承受热应激的能力产生了严重影响。这与panA敲除的情况形成对比,panA敲除显示出耐热性增强。总之,这些结果为蛋白酶体在古菌中的生物学作用提供了新的重要见解。