Protists: Eukaryotic single-celled organisms and the functioning of their organelles.

Advances in microbial physiology Pub Date : 2024-01-01 Epub Date: 2024-03-16 DOI:10.1016/bs.ampbs.2024.02.001
Nigel Yarlett, Edward L Jarroll, Mary Morada, David Lloyd
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Abstract

Organelles are membrane bound structures that compartmentalize biochemical and molecular functions. With improved molecular, biochemical and microscopy tools the diversity and function of protistan organelles has increased in recent years, providing a complex panoply of structure/function relationships. This is particularly noticeable with the description of hydrogenosomes, and the diverse array of structures that followed, having hybrid hydrogenosome/mitochondria attributes. These diverse organelles have lost the major, at one time, definitive components of the mitochondrion (tricarboxylic cycle enzymes and cytochromes), however they all contain the machinery for the assembly of Fe-S clusters, which is the single unifying feature they share. The plasticity of organelles, like the mitochondrion, is therefore evident from its ability to lose its identity as an aerobic energy generating powerhouse while retaining key ancestral functions common to both aerobes and anaerobes. It is interesting to note that the apicoplast, a non-photosynthetic plastid that is present in all apicomplexan protozoa, apart from Cryptosporidium and possibly the gregarines, is also the site of Fe-S cluster assembly proteins. It turns out that in Cryptosporidium proteins involved in Fe-S cluster biosynthesis are localized in the mitochondrial remnant organelle termed the mitosome. Hence, different organisms have solved the same problem of packaging a life-requiring set of reactions in different ways, using different ancestral organelles, discarding what is not needed and keeping what is essential. Don't judge an organelle by its cover, more by the things it does, and always be prepared for surprises.

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原生生物真核单细胞生物及其细胞器的功能。
细胞器是一种膜结合结构,可分隔生化和分子功能。近年来,随着分子、生物化学和显微镜工具的改进,原生动物细胞器的多样性和功能不断增加,提供了复杂的结构/功能关系。这一点在氢体的描述以及随后出现的具有氢体/半胱混合属性的各种结构中尤为明显。这些不同的细胞器失去了线粒体的主要成分(三羧酸循环酶和细胞色素),但它们都含有组装 Fe-S 簇的机制,这是它们唯一的共同特征。因此,细胞器(如线粒体)的可塑性体现在它能够在保留有氧生物和厌氧生物共同的关键祖先功能的同时,失去有氧生物能量生成动力的特性。值得注意的是,除了隐孢子虫和可能的革兰氏原虫之外,存在于所有类囊原生动物中的非光合质体--顶体,也是 Fe-S 簇组装蛋白的所在地。事实证明,在隐孢子虫中,参与 Fe-S 簇生物合成的蛋白质定位于线粒体残余细胞器(称为有丝分裂体)中。因此,不同的生物以不同的方式,利用不同的祖先细胞器,丢弃不需要的东西,保留必要的东西,解决了包装生命所需的一系列反应的相同问题。不要根据细胞器的外表来判断它的好坏,而是要根据它的功能来判断它的好坏,并且要时刻准备迎接惊喜。
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