矿物质和非矿物质来源的铁和硫对巴氏拟尾柱虫金属蛋白质组的影响

IF 3.9 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Applied and Environmental Microbiology Pub Date : 2024-08-21 Epub Date: 2024-07-18 DOI:10.1128/aem.00516-24
James Larson, Monika Tokmina-Lukaszewska, Devon Payne, Rachel L Spietz, Hunter Fausset, Md Gahangir Alam, Brooklyn K Brekke, Jordan Pauley, Ethan J Hasenoehrl, Eric M Shepard, Eric S Boyd, Brian Bothner
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引用次数: 0

摘要

甲烷菌通常栖息在硫酸环境中,这种环境有利于铁(Fe)等过渡金属沉淀为金属硫化物,包括麦饭石(FeS)和黄铁矿(FeS2)。这些金属硫化物历来被认为是生物无法利用的。然而,甲烷菌通常以硫化物(HS-)作为硫源进行培养,这种情况预计会有利于金属沉淀,从而限制金属的可用性。最近的研究表明,甲烷菌可以从 FeS 和 FeS2 中获取铁和硫(S)来维持生长。因此,与提供 HS- 的培养基相比,提供 FeS2 的培养基应能提供更多的过渡金属。在此,我们研究了硫酸(即细胞以 HS- 作为唯一的 S 源)与非硫酸(细胞以 FeS2 作为唯一的 S 源)条件下过渡金属的可用性如何影响 Methanosarcina barkeri Fusaro 的金属蛋白质组。为此,我们采用了尺寸排阻色谱法结合电感耦合等离子体质谱法和枪式蛋白质组学。我们观察到铁、钴、镍、锌和钼蛋白质的组成和丰度发生了显著变化。在这些差异中,参与甲烷生成和电子传递链的多亚基蛋白质复合物的化学计量和丰度也发生了变化。我们的数据表明,M. barkeri在FeS2上生长时利用最小的铁硫簇复合体和典型的半胱氨酸生物合成蛋白,但在硫酸生长条件下则利用典型的Suf途径与tRNA-Sep半胱氨酸途径结合进行铁硫簇和半胱氨酸的生物合成。因此,金属和硫的供应相互交织,对生物体的生物化学有很大影响。甲烷菌通常生活在缺氧、富含硫化物(富氧)的环境中,这种环境有利于过渡金属以金属硫化物的形式沉淀,从而造成假定的金属限制。黄铁矿是一种丰富的硫化铁矿物,传统上被认为是生物无法利用的。本文介绍的研究工作为我们提供了新的视角,让我们了解在黄铁矿生长条件下生长的 Methanosarcina barkeri Fusaro 的金属蛋白分布和金属吸收情况。对这种甲烷菌在不同金属和硫条件下的特征进行的深入研究,增加了我们对金属可用性对甲烷菌(可能还有其他栖息在戊辛基环境中的厌氧菌)的影响的了解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Impact of mineral and non-mineral sources of iron and sulfur on the metalloproteome of Methanosarcina barkeri.

Methanogens often inhabit sulfidic environments that favor the precipitation of transition metals such as iron (Fe) as metal sulfides, including mackinawite (FeS) and pyrite (FeS2). These metal sulfides have historically been considered biologically unavailable. Nonetheless, methanogens are commonly cultivated with sulfide (HS-) as a sulfur source, a condition that would be expected to favor metal precipitation and thus limit metal availability. Recent studies have shown that methanogens can access Fe and sulfur (S) from FeS and FeS2 to sustain growth. As such, medium supplied with FeS2 should lead to higher availability of transition metals when compared to medium supplied with HS-. Here, we examined how transition metal availability under sulfidic (i.e., cells provided with HS- as sole S source) versus non-sulfidic (cells provided with FeS2 as sole S source) conditions impact the metalloproteome of Methanosarcina barkeri Fusaro. To achieve this, we employed size exclusion chromatography coupled with inductively coupled plasma mass spectrometry and shotgun proteomics. Significant changes were observed in the composition and abundance of iron, cobalt, nickel, zinc, and molybdenum proteins. Among the differences were alterations in the stoichiometry and abundance of multisubunit protein complexes involved in methanogenesis and electron transport chains. Our data suggest that M. barkeri utilizes the minimal iron-sulfur cluster complex and canonical cysteine biosynthesis proteins when grown on FeS2 but uses the canonical Suf pathway in conjunction with the tRNA-Sep cysteine pathway for iron-sulfur cluster and cysteine biosynthesis under sulfidic growth conditions.IMPORTANCEProteins that catalyze biochemical reactions often require transition metals that can have a high affinity for sulfur, another required element for life. Thus, the availability of metals and sulfur are intertwined and can have large impacts on an organismismal biochemistry. Methanogens often occupy anoxic, sulfide-rich (euxinic) environments that favor the precipitation of transition metals as metal sulfides, thereby creating presumed metal limitation. Recently, several methanogens have been shown to acquire iron and sulfur from pyrite, an abundant iron-sulfide mineral that was traditionally considered to be unavailable to biology. The work presented here provides new insights into the distribution of metalloproteins, and metal uptake of Methanosarcina barkeri Fusaro grown under euxinic or pyritic growth conditions. Thorough characterizations of this methanogen under different metal and sulfur conditions increase our understanding of the influence of metal availability on methanogens, and presumably other anaerobes, that inhabit euxinic environments.

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来源期刊
Applied and Environmental Microbiology
Applied and Environmental Microbiology 生物-生物工程与应用微生物
CiteScore
7.70
自引率
2.30%
发文量
730
审稿时长
1.9 months
期刊介绍: Applied and Environmental Microbiology (AEM) publishes papers that make significant contributions to (a) applied microbiology, including biotechnology, protein engineering, bioremediation, and food microbiology, (b) microbial ecology, including environmental, organismic, and genomic microbiology, and (c) interdisciplinary microbiology, including invertebrate microbiology, plant microbiology, aquatic microbiology, and geomicrobiology.
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