Campanella Jonatas Erick Maimoni, Rosa Leonardo Talachia, Malavazi Iran
Departamento de Genética e Evolução, Centro de Ciências Biológicas e da Saúde, Universidade Federal de São Carlos (UFSCar), São Paulo, Brazil.
Department of Biochemistry and Tissue Biology, Biology Institute, Universidade Estadual de Campinas (UNICAMP), São Paulo, Brazil.
mBio. 2025 Aug 13;16(8):e0080324. doi: 10.1128/mbio.00803-24. Epub 2025 Jun 26.
, , and are the leading fungal pathogens that cause life-threatening deep mycosis, posing significant challenges to immunocompromised patients and increasing healthcare costs worldwide. Lipid metabolism is crucial for the growth and development of all organisms. Increasing evidence highlights that complex structural lipids in the fungal cell membrane emerge as important factors involved in cell signaling, stress response, and immune recognition. Membrane fluidity is primarily regulated by the ratio of saturated and unsaturated fatty acids (UFAs), structural components of membrane phospholipids, and sphingolipids, which comprise UFAs with varying degrees of unsaturation. A notable group of UFA found in these molecules contains a double bond located at the C9 position of the carbon chain. The synthesis of such molecules is dependent on Δ9-fatty acid (FA) desaturase enzymes. In the absence of Δ9-FA desaturase, fungal cells become auxotrophic for palmitoleic and oleic acids (C16 and C18 UFA, respectively), suggesting that this essential enzyme family is fundamental for fungal physiology and virulence. However, the extent of phenotypes and especially the biochemical properties of fungal Δ9-FA desaturases remain poorly understood. In this manuscript, we summarize the current information and fundamental findings on Δ9-FA desaturase, gathered from functional studies on relevant fungal pathogens with a focus on or deduced from model organisms, including yeasts and their mammalian counterparts. We also discuss its unique domain organization and its implications for the catalytic mechanism and the potential of fungal Δ9-FA desaturase as a chemotherapeutic target.
曲霉属、念珠菌属和隐球菌属是导致危及生命的深部真菌病的主要真菌病原体,给免疫功能低下的患者带来了重大挑战,并增加了全球的医疗成本。脂质代谢对所有生物体的生长和发育至关重要。越来越多的证据表明,真菌细胞膜中的复杂结构脂质是参与细胞信号传导、应激反应和免疫识别的重要因素。膜流动性主要由膜磷脂和鞘脂的结构成分饱和脂肪酸和不饱和脂肪酸(UFA)的比例调节,鞘脂包含不同程度不饱和的UFA。在这些分子中发现的一组值得注意的UFA在碳链的C9位置含有一个双键。此类分子的合成依赖于Δ9-脂肪酸(FA)去饱和酶。在缺乏Δ9-FA去饱和酶的情况下,真菌细胞对棕榈油酸和油酸(分别为C16和C18 UFA)成为营养缺陷型,这表明这个必需的酶家族对真菌生理和毒力至关重要。然而,真菌Δ9-FA去饱和酶的表型范围,尤其是其生化特性仍知之甚少。在本手稿中,我们总结了关于Δ9-FA去饱和酶的当前信息和基本发现,这些信息来自对相关真菌病原体的功能研究,重点是曲霉属,或从包括酵母及其哺乳动物对应物在内的模式生物中推导得出。我们还讨论了其独特的结构域组织及其对催化机制的影响以及真菌Δ9-FA去饱和酶作为化疗靶点的潜力。