
海洋赤杆菌科菌株的类胡萝卜素合成基因分析
Investigation of carotenoid biosynthesis genes in marine Erythrobacteraceae strains
赤杆菌科(Erythrobacteraceae)菌株广泛分布于海洋环境,可合成类胡萝卜素等多种色素。类胡萝卜素具有光保护和抗氧化能力,对于赤杆菌科菌株适应海洋生态系统具有重要作用。本研究收集了107个海洋来源的赤杆菌科细菌基因组,分析了类胡萝卜素合成途径中关键酶的编码基因crtEBIGYZW在基因组中的分布特征,构建了基于氨基酸序列的不同编码基因系统发育树,阐明了深海和浅海来源的赤杆菌科菌株中类胡萝卜素合成基因的存在和分布规律,探究了不同的类胡萝卜素合成基因在近海与深海来源的赤杆菌科菌株进化过程中的遗传模式。研究结果显示,海洋来源的赤杆菌科菌株均含有crtEIGZ基因,约98.1%的菌株含有crtBY基因,约43.9%的菌株中存在crtW基因,其类胡萝卜素合成基因在菌株间存在分布差异,但在深海与浅海来源上并未显示特异性。此外,通过比较不同编码基因的系统发育树拓扑结构发现,赤杆菌科菌株的类胡萝卜素合成基因crtBYZW与系统发育密切相关,而crtEIG基因多通过水平基因转移获得,这有助于更好地评估类胡萝卜素合成基因家族在赤杆菌科中的进化,也为其他海洋细菌中的类胡萝卜素合成途径及基因研究提供科学依据,从而有助于开发海洋来源的产类胡萝卜素菌株。
Erythrobacteraceae is widely distributed in marine environments and can synthesize various pigments such as carotenoids. Carotenoids have photoprotective and antioxidant abilities, and they can play a crucial role in the adaptation of Erythrobacteraceae to marine ecosystems. In this study, we obtained the genomes of 107 marine Erythrobacteriaceae strains, analyzed the distribution characteristics of carotenoid biosynthesis genes including crtEBIGYZW in their genomes, constructed phylogenetic trees based on the amino acid sequences of the carotenoid biosynthesis genes, and elucidated the presence and distribution of carotenoid biosynthesis genes in Erythrobacteriaceae from deep-sea and shallow-sea sources. The results suggested that all of marine Erythrobacteriaceae strains contained the crtEIGZ genes, 98.1% of strains contained the crtBY genes, and 43.9% of them contained the crtW gene, which differed among strains but no any specificities found among the deep-sea or shallow-sea sources. Additionally, in the comparison of the phylogenetic topology, it was found that the crtBYZW genes were vertically transferred from their ancestor, while the crtEIG genes were mainly horizontal gene transferred. Our study aids in the understanding of the carotenoid biosynthesis gene evolution in the family Erythrobacteriaceae and also serves as a scientific basis for the study of carotenoid synthesis pathways and genes in other marine bacteria, enables a thorough understanding of marine carotenoid-synthesizing strains.
赤杆菌科 / 海洋 / 类胡萝卜素合成基因 / 系统发育 / 进化
Erythrobacteriaceae / marine / carotenoid biosynthesis gene / phylogeny / evolution
[1] |
吴月红, 许学伟. 赤杆菌科微生物分类研究进展[J]. 微生物学通报, 2016, 43(5):1082-1094.
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[2] |
The family, belonging to the order, class, is globally distributed in various environments. Currently, this family consist of seven genera:,,,,, and. As more species are identified, the taxonomic status of the family should be revised at the genomic level because of its polyphyletic nature evident from 16S rRNA gene sequence analysis. Phylogenomic reconstruction based on 288 single-copy orthologous clusters led to the identification of three separate clades. Pairwise comparisons of average nucleotide identity, average amino acid identity (AAI), percentage of conserved protein and evolutionary distance indicated that AAI and evolutionary distance had the highest correlation. Thresholds for genera boundaries were proposed as 70 % and 0.4 for AAI and evolutionary distance, respectively. Based on the phylo-genomic and genomic similarity analysis, the three clades were classified into 16 genera, including 11 novel ones, for which the names,,,,,,,,, and are proposed. We reclassified all species of and as species of. This study is the first genomic-based study of the family, and will contribute to further insights into the evolution of this family.
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[3] |
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[4] |
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[5] |
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[6] |
Carotenoids are lipid-soluble pigments that are produced in some plants, algae, fungi, and bacterial species, which accounts for their orange and yellow hues. Carotenoids are powerful antioxidants thanks to their ability to quench singlet oxygen, to be oxidized, to be isomerized, and to scavenge free radicals, which plays a crucial role in the etiology of several diseases. Unusual marine environments are associated with a great chemical diversity, resulting in novel bioactive molecules. Thus, marine organisms may represent an important source of novel biologically active substances for the development of therapeutics. In this respect, various novel marine carotenoids have recently been isolated from marine organisms and displayed several utilizations as nutraceuticals and pharmaceuticals. Marine carotenoids (astaxanthin, fucoxanthin, β-carotene, lutein but also the rare siphonaxanthin, sioxanthin, and myxol) have recently shown antioxidant properties in reducing oxidative stress markers. This review aims to describe the role of marine carotenoids against oxidative stress and their potential applications in preventing and treating inflammatory diseases.
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[7] |
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[8] |
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[9] |
Carotenoids are ubiquitous pigments synthesized by plants, fungi, algae, and bacteria. Industrially, carotenoids are used in pharmaceuticals, neutraceuticals, and animal feed additives, as well as colorants in cosmetics and foods. Scientific interest in dietary carotenoids has increased in recent years because of their beneficial effects on human health, such as lowering the risk of cancer and enhancement of immune system function, which are attributed to their antioxidant potential. The availability of carotenoid genes from carotenogenic microbes has made possible the synthesis of carotenoids in non-carotenogenic microbes. The increasing interest in microbial sources of carotenoid is related to consumer preferences for natural additives and the potential cost effectiveness of creating carotenoids via microbial biotechnology. In this review, we will describe the recent progress made in metabolic engineering of non-carotenogenic microorganisms with particular focus on the potential of Escherichia coli for improved carotenoid productivity.
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[10] |
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[11] |
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[12] |
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[13] |
A fundamental question in microbiology is whether there is continuum of genetic diversity among genomes, or clear species boundaries prevail instead. Whole-genome similarity metrics such as Average Nucleotide Identity (ANI) help address this question by facilitating high resolution taxonomic analysis of thousands of genomes from diverse phylogenetic lineages. To scale to available genomes and beyond, we present FastANI, a new method to estimate ANI using alignment-free approximate sequence mapping. FastANI is accurate for both finished and draft genomes, and is up to three orders of magnitude faster compared to alignment-based approaches. We leverage FastANI to compute pairwise ANI values among all prokaryotic genomes available in the NCBI database. Our results reveal clear genetic discontinuity, with 99.8% of the total 8 billion genome pairs analyzed conforming to >95% intra-species and <83% inter-species ANI values. This discontinuity is manifested with or without the most frequently sequenced species, and is robust to historic additions in the genome databases.
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[14] |
The multiplex capability and high yield of current day DNA-sequencing instruments has made bacterial whole genome sequencing a routine affair. The subsequent de novo assembly of reads into contigs has been well addressed. The final step of annotating all relevant genomic features on those contigs can be achieved slowly using existing web- and email-based systems, but these are not applicable for sensitive data or integrating into computational pipelines. Here we introduce Prokka, a command line software tool to fully annotate a draft bacterial genome in about 10 min on a typical desktop computer. It produces standards-compliant output files for further analysis or viewing in genome browsers.Prokka is implemented in Perl and is freely available under an open source GPLv2 license from http://vicbioinformatics.com/.© The Author 2014. Published by Oxford University Press. All rights reserved. For Permissions, please e-mail: journals.permissions@oup.com.
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[15] |
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[16] |
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[17] |
We report a major update of the MAFFT multiple sequence alignment program. This version has several new features, including options for adding unaligned sequences into an existing alignment, adjustment of direction in nucleotide alignment, constrained alignment and parallel processing, which were implemented after the previous major update. This report shows actual examples to explain how these features work, alone and in combination. Some examples incorrectly aligned by MAFFT are also shown to clarify its limitations. We discuss how to avoid misalignments, and our ongoing efforts to overcome such limitations.
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[18] |
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[19] |
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[20] |
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[21] |
Thermo (or hyperthermo) philic microorganisms are ubiquitous having a wide range of habitats from freshly fallen snow to pasteurized milk to geothermal areas like hot springs. The variations in physicochemical conditions, viz., temperature, pH, nutrient availability and light intensity in the habitats always pose stress conditions for the inhabitants leading to slow growth or cell death. The industrial processes used for harvesting secondary metabolites such as enzymes, toxins and organic acids also create stressed environments for thermophiles. The production of DNA-binding proteins, activation of reactive oxygen species detoxification system, compatible solute accumulation, expression of heat shock proteins and alterations in morphology are a few examples of physiological changes demonstrated by these microscopic lifeforms in stress. These microorganisms exhibit complex genetic and physiological changes to minimize, adapt to and repair damage caused by extreme environmental disturbances. These changes are termed as 'stress responses' which enable them to stabilize their homeostasis. The exploration of important thermophilic factors would pave the way in engineering the microbial strains for various biotechnological applications. This review article presents a picture of physiological responses of thermophiles against various stress conditions as their mechanisms to respond to stress make them model organisms to further explore them for basic and applied biology purposes.
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[22] |
Microorganisms engage in complex interactions with other members of the microbial community, higher organisms as well as their environment. However, determining the exact nature of these interactions can be challenging due to the large number of members in these communities and the manifold of interactions they can engage in. Various omic data, such as 16S rRNA gene sequencing, shotgun metagenomics, metatranscriptomics, metaproteomics and metabolomics, have been deployed to unravel the community structure, interactions and resulting community dynamics in situ. Interpretation of these multi-omic data often requires advanced computational methods. Modelling approaches are powerful tools to integrate, contextualize and interpret experimental data, thus shedding light on the underlying processes shaping the microbiome. Here, we review current methods and approaches, both experimental and computational, to elucidate interactions in microbial communities and to predict their responses to perturbations.© 2017 The Authors. Microbial Biotechnology published by John Wiley & Sons Ltd and Society for Applied Microbiology.
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[23] |
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[24] |
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[25] |
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[26] |
Microorganisms are ubiquitous on Earth and can inhabit almost every environment. In a complex heterogeneous environment or in face of ecological disturbance, the microbes adjust to fluctuating environmental conditions through a cascade of cellular and molecular systems. Their habitats differ from cold microcosms of Antarctica to the geothermal volcanic areas, terrestrial to marine, highly alkaline zones to the extremely acidic areas and freshwater to brackish water sources. The diverse ecological microbial niches are attributed to the versatile, adaptable nature under fluctuating temperature, nutrient availability and pH of the microorganisms. These organisms have developed a series of mechanisms to face the environmental changes and thereby keep their role in mediate important ecosystem functions. The underlying mechanisms of adaptable microbial nature are thoroughly investigated at the cellular, genetic and molecular levels. The adaptation is mediated by a spectrum of processes like natural selection, genetic recombination, horizontal gene transfer, DNA damage repair and pleiotropy-like events. This review paper provides the fundamentals insight into the microbial adaptability besides highlighting the molecular network of microbial adaptation under different environmental conditions.© 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.
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[27] |
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[28] |
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[29] |
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[30] |
A 37-kb photosynthesis gene cluster was sequenced in a photosynthetic bacterium belonging to the beta subclass of purple bacteria (Proteobacteria), Rubrivivax gelatinosus. The cluster contained 12 bacteriochlorophyll biosynthesis genes (bch), 7 carotenoid biosynthesis genes (crt), structural genes for photosynthetic apparatuses (puf and puh), and some other related genes. The gene arrangement was markedly different from those of other purple photosynthetic bacteria, while two superoperonal structures, crtEF-bchCXYZ-puf and bchFNBHLM-lhaA-puhA, were conserved. Molecular phylogenetic analyses of these photosynthesis genes showed that the photosynthesis gene cluster of Rvi. gelatinosus was originated from those of the species belonging to the alpha subclass of purple bacteria. It was concluded that a horizontal transfer of the photosynthesis gene cluster from an ancestral species belonging to the alpha subclass to that of the beta subclass of purple bacteria had occurred and was followed by rearrangements of the operons in this cluster.
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[31] |
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[32] |
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[33] |
Marine bacteria have not been examined as extensively as land bacteria. We screened carotenoids from orange or red pigments-producing marine bacteria belonging to rare or novel species. The new acyclic carotenoids with a C₃₀ aglycone, diapolycopenedioc acid xylosylesters A-C and methyl 5-glucosyl-5,6-dihydro-apo-4,4'-lycopenoate, were isolated from the novel Gram-negative bacterium Rubritalea squalenifaciens, which belongs to phylum Verrucomicrobia, as well as the low-GC Gram-positive bacterium Planococcus maritimus strain iso-3 belonging to the class Bacilli, phylum Firmicutes, respectively. The rare monocyclic C₄₀ carotenoids, (3R)-saproxanthin and (3R,2'S)-myxol, were isolated from novel species of Gram-negative bacteria belonging to the family Flavobacteriaceae, phylum Bacteroidetes. In this review, we report the structures and antioxidant activities of these carotenoids, and consider relationships between bacterial phyla and carotenoid structures.
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[34] |
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[35] |
|
[36] |
|
[37] |
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[38] |
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