Rai Ashutosh K, Sawasato Katsuhiro, Bennett Haley C, Kozlova Anastasiia, Sparagna Genevieve C, Bogdanov Mikhail, Mitchell Angela M
Department of Biology, Texas A&M University, College Station, Texas, USA.
Department of Biochemistry and Molecular Biology, McGovern Medical School at The University of Texas Health Science Center at Houston, Houston, Texas, USA.
bioRxiv. 2024 May 21:2023.06.21.545913. doi: 10.1101/2023.06.21.545913.
The outer membrane of Gram-negative bacteria is a barrier to chemical and physical stress. Phospholipid transport between the inner and outer membranes has been an area of intense investigation and, in K-12, it has recently been shown to be mediated by YhdP, TamB, and YdbH, which are suggested to provide hydrophobic channels for phospholipid diffusion, with YhdP and TamB playing the major roles. However, YhdP and TamB have different phenotypes suggesting distinct functions. We investigated these functions using synthetic cold sensitivity (at 30 °C) caused by deletion of and , a transcriptional regulator controlling fatty acid degradation and unsaturated fatty acid production, but not by Δ Δ or Δ Δ,. Deletion of suppresses the Δ Δ cold sensitivity suggesting this phenotype is related to phospholipid transport. The Δ Δ strain shows a greater increase in cardiolipin upon transfer to the non-permissive temperature and genetically lowering cardiolipin levels can suppress cold sensitivity. These data also reveal a qualitative difference between cardiolipin synthases in , as deletion of suppresses cold sensitivity but deletion of does not despite lower cardiolipin levels. In addition to increased cardiolipin, increased fatty acid saturation is necessary for cold sensitivity and lowering this level genetically or through supplementation of oleic acid suppresses the cold sensitivity of the Δ Δ strain. Although indirect effects are possible, we favor the parsimonious hypothesis that YhdP and TamB have differential substrate transport preferences, most likely with YhdP preferentially transporting more saturated phospholipids and TamB preferentially transporting more unsaturated phospholipids. We envision cardiolipin contributing to this transport preference by sterically clogging TamB-mediated transport of saturated phospholipids. Thus, our data provide a potential mechanism for independent control of the phospholipid composition of the inner and outer membranes in response to changing conditions.
革兰氏阴性菌的外膜是抵御化学和物理应激的一道屏障。内膜与外膜之间的磷脂转运一直是深入研究的领域,在K - 12菌株中,最近发现其由YhdP、TamB和YdbH介导,这些蛋白被认为为磷脂扩散提供疏水通道,其中YhdP和TamB起主要作用。然而,YhdP和TamB具有不同的表型,表明它们具有不同的功能。我们利用合成冷敏感性(在30°C)来研究这些功能,这种冷敏感性是由缺失 和 引起的, 是一种控制脂肪酸降解和不饱和脂肪酸产生的转录调节因子,但Δ Δ 或Δ Δ 不会导致这种情况。缺失 可抑制Δ Δ 的冷敏感性,表明这种表型与磷脂转运有关。Δ Δ 菌株在转移到非允许温度时心磷脂增加得更多,通过基因手段降低心磷脂水平可抑制冷敏感性。这些数据还揭示了 中心磷脂合酶之间的质的差异,因为缺失 可抑制冷敏感性,但缺失 尽管心磷脂水平较低却不能抑制冷敏感性。除了心磷脂增加外,脂肪酸饱和度增加对于冷敏感性也是必要的,通过基因手段降低或通过补充油酸来降低这种水平可抑制Δ Δ 菌株的冷敏感性。尽管可能存在间接影响,但我们倾向于一种简约的假设,即YhdP和TamB具有不同的底物转运偏好,最有可能是YhdP优先转运更多饱和磷脂,而TamB优先转运更多不饱和磷脂。我们设想心磷脂通过空间位阻阻碍TamB介导的饱和磷脂转运来促成这种转运偏好。因此,我们的数据为响应变化的条件独立控制内膜和外膜的磷脂组成提供了一种潜在机制。