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    Home > Biochemistry News > Microbiology News > The same team from the Shenzhen Advanced Institute of the Chinese Academy of Sciences explored the mystery of the origin of eukaryotic cell membrane lipids through synthetic biology

    The same team from the Shenzhen Advanced Institute of the Chinese Academy of Sciences explored the mystery of the origin of eukaryotic cell membrane lipids through synthetic biology

    • Last Update: 2023-01-01
    • Source: Internet
    • Author: User
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    On November 24, 2022, the research group of Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, in collaboration with the research group of Professor Zhang Chuanlun of Southern University of Science and Technology, published a title entitled Angewandte Chemie International Edition Biosynthesis of Hybrid Neutral Lipids with Archaeal and Eukaryotic Research paper by Characteristics in Engineered Saccharomyces cerevisiae.



    Relying on the major scientific and technological infrastructure of synthetic biology research in Shenzhen (hereinafter referred to as the "big facility" of synthetic biology), the research team used Saccharomyces cerevisiae as the chassis to realize the heterologous synthesis of archaeal polar cell membrane lipids in eukaryotic cells for the first time, and accidentally observed heterozygous neutral lipids (DGGGO-FA) with both eukaryotic and archaeal characteristics



    The research team further analyzed the synthesis mechanism of this novel compound, and proposed and partially verified the hypothesis that triacylglycerol (TAG) molecules may be synthesized by archaea for energy storage through bioinformation analysis and experimental characterization, which challenged the general understanding of the scientific community
    .


    The tree of life is divided into three domains: bacteria, eukary, and Archaea
    .


    In 1977, American microbiologist Carl Woese stumbled upon archaea through 16S/18S rRNA sequence phylogenetic analysis, according to which prokaryotes were divided into two categories: bacteria and archaea, and together with eukaryotes constitute the three-domain system of the origin of life Three-Domain Hypothesis (Three-Domain).


    James, 1988 Based on the classification method of ribosome structural similarity and evolutionary simplicity, Lake revealed that eukaryotes are a branch of archaea, suggesting that eukaryotes may be derived from archaea, and proposed the two-domain system tree of life hypothesis
    .
    Archaea are single-celled prokaryotic microorganisms, without nuclei, without endometrial system, with circular genomes and lack of splicing introns in the body, which are close to bacteria in cell structure and metabolism; But in the central processes of biology such as DNA replication, transcription and translation, it is more closely
    related to eukaryotes.
    Humans belong to eukaryotes
    .
    Are archaea siblings of eukaryotes
    (three-domain hypothesis) or parents (two-domain hypothesis)? This is one of the great problems in the evolution of
    life.


    Three-domain system


    Two-domain system


    The development of metagenomic technology has led to the discovery of Asgard archaea, many of whose genomes carry a large number of eukaryotic signatures Proteins, ESP) encodes genes and is evolutionarily the closest prokaryotic
    organism to eukaryotic origin.


    The discovery of Asgard archaea is thought to favor the two-domain system tree of life hypothesis: about 18-2 billion years ago, the archaeal ancestors of the Asgard lineage first acquired a primitive cytoskeletal system with membrane deformation and the ability to sort and transport nuclear endosomal material, and then developed an "endosymbiosis" with the bacteria of the Alpha Proteobacteria phylum, and gradually evolved into the most important cell line in modern eukaryotes, mitochondria, which became a key step
    in the origin of eukaryotes.


    However, endosymbiosis also faces many challenges, one of which is an important unsolved mystery is why the membrane lipomolecular backbone of existing eukaryotic cells and archaeal cells has opposite chirality.
    The membrane lipids of modern bacteria and eukaryotic cells are mainly composed of glycerol-3-phosphate
    (G3P) as the skeleton, while archaeal cell membranes use glycerol-1-phosphate (G1P) as the basic parent nuclear structure, a phenomenon known as Lipid Divide
    .
    This phenomenon is extremely unusual because the organic molecules that make up life on Earth usually have a single chirality, such as L-type amino acids, D-type nucleotides, and so on
    .
    Based on the endosymbiosis theory, modern eukaryotic cells should be derived from archaeal hosts, but their membrane lipids have the opposite chirality to archaea and are similar
    to those of endocytosed bacteria.
    There seems to be an irreconcilable contradiction between the membrane lipid demarcation and the two-domain tree of life, which is one of the great mysteries of
    eukaryotic origin.
    In previous studies, scientists
    have constructed heterozygous membrane lipid models with both G1P and G3P based on liposomes and bacteria, but have not yet successfully constructed eukaryotic-archaeal heterozygous models to more directly study the origin of
    eukaryotic membrane lipids.


    Saccharomyces cerevisiae is a model eukaryotic microorganism with detailed genetic biochemical studies and rich synthetic biology tools, which is an ideal host
    for studying the evolution of archaea-eukaryotic membrane lipids 。 Relying on the "big facility" of synthetic biology, the authors used modular DNA assembly methods to construct a biosynthetic pathway of polar lipids in archaeal cell membranes on a large scale, and introduced key synthetic genes from different sources such as methanogenic archaea, sulfide archaea, and Asgard archaea in a "plug and play" manner in the yeast chassis, and successfully synthesized polar lipids with archaeal ether bond characteristics
    (Figure 1).

    Based on this model, the authors found that Saccharomyces cerevisiae also has the ability
    to synthesize G1P.
    At the same time, the authors obtained the first biochemical experimental evidence to support the synthesis of Heterozygous membrane lipids with both G1P and G3P chiral GRGGPS enzymes derived from Asgard archaea
    (Figure 2).

    These observations suggest that the membrane lipid demarcation is not as strict
    as originally thought.


    Figure 1: Synthesis pathway of characteristic lipids of archaea in recombinant yeast (blue background) and endogenous lipid synthesis pathway of yeast (yellow background)
    Figure 2a, synthesis of Gty-Ma lipids in recombinant yeast, ion peak 1-4: archaeal polar lipids; Blue background ion peak: 5, unsaturated archanol DGGGOH; Other, DGGGO-FAs; Yellow background ion peak: yeast endogenous TAG.

    b, Functional characterization
    of key enzymes/pathways for polar lipid synthesis in archaeal cell membranes.

    Notably, the authors accidentally discovered a series of neutral lipid molecules in recombinant yeast (Figure 2, ion peak on blue background).

    The authors used NMR, high-resolution mass spectrometry, tandem mass spectrometry and other analytical methods to identify the molecular structure of these compounds as novel heterozygous neutral lipid DGGGO-FAs, which contained archaeal ether bond characteristics and bacterial fatty acyl group characteristics
    .
    Based on gene knockout, replenishment and other methods, the authors explored the biosynthesis mechanism of DGGGO-FAs, and found that the diacylglycerol acyltransferase DGAT in Saccharomyces cerevisiae is a key synthetase, which catalyzes the condensation of DGGGOH archaeol and Acyl-CoA to produce DGGGO-FA.


    Excitingly, the authors performed a DGAT sequence homologous search in the archaeal protein database and found that its isoenzyme sequences were widely distributed
    across the archaeal domain.
    The authors selected DGAT sequences derived from
    Candidatus Bathyarchaeota and Euryarchaeota and proved that archaeal DGAT enzymes have the ability to synthesize DGGGO-FA through heterologous expression in yeast.
    At the same time, it can also catalyze the synthesis of TAG molecules
    .
    In nature, polyhydroxyalkanoates
    (PHA), TAG and wax esters (Wax Ester) and other neutral lipids are usually used for energy storage, of which eukaryotes and bacteria mainly use PHA, Wax Ester and TAG, and archaea mainly use PHA
    .
    In this study, the authors demonstrated for the first time that DGAT enzymes are widely present in archaea
    (Figure 3) and demonstrated their ability to synthesize DGGGO-FAs through biochemical experiments, which is expected to rewrite the scientific community's understanding
    of the form of energy storage in archaea.
    However, it is unclear whether archaea can synthesize DGGGO-FA neutral lipids in the natural environment, so the hypothesis proposed in this study still needs to be further tested
    .

    Figure 3: DGAT isoenzymes are widely distributed
    in bacteria, eukaryotes and archaea In short, there are still many controversies and unsolved mysteries about the origin of eukaryotic life, and synthetic biology can provide new ideas and methods
    。 One of the limitations of this study is that the content of polar lipids in archaeal cell membranes in yeast models is still low, failing to convincingly answer the question
    of whether heterozygous cell membranes are stable in eukaryotic cells.
    In the future, the authors plan to combine metabolic engineering and other methods to improve the efficiency of heterologous synthesis of archaea membrane lipids, study the influence of membrane lipid chirality on key life processes such as eukaryotic cell physiology and lipid subcell localization, and continue to explore the mystery of the origin and evolution of eukaryotic cell membrane lipids
    .

    Assistant researcher Zhang Jianzhi of Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences is the first author, and researcher Si Tong is the corresponding author
    .

    The research was supported by the National Key Research and Development Program of China (2021YFA0910800 and 2020YFA0908500), the National Natural Science Foundation of China (32101179, 32071428, 91851210), Funded by Shenzhen Key Laboratory of Marine Geoarchomics (ZDSYS201802081843490) and Southern Marine Science and Engineering Guangdong Laboratory (Guangzhou), and supported by Shenzhen Innovation Institute of Synthetic Biology
    .

    Paper link: https://doi.
    org/10.
    1002/anie.
    202214344

    PI and the introduction of the research group

    Si Tong, researcher and doctoral supervisor
    of the Institute of Synthetic Biology, Shenzhen Advanced Institute, Chinese Academy of Sciences.
    Chief scientist of the synthetic biology project of the National Key R&D Program, national high-level talent (youth), chief technologist of major scientific and technological infrastructure for
    synthetic biology research in Shenzhen 。 The research group is automated synthetic biotechnology, including machine learning-guided protein engineering, high-throughput mass spectrometry screening, etc.
    , for the development of microbial cell factories to research and produce important molecules such as fuels, chemicals, and drugs, and the preliminary results are in Nature Communications, JACS, Angew Chemie, Metabolic Engineering and other internationally renowned academic journals have published more than 50 papers, and "Google Scholar" has been cited more than 2400 times
    .

    The main research direction of the research group is automated synthetic biotechnology, relying on the major scientific and technological infrastructure of synthetic biology research in Shenzhen, adopting a data-driven design-build-test-learning closed-loop research paradigm to carry out research
    on protein engineering, cell factories, natural products and so on.
    Long-term recruitment of synthetic biology, instrumental analysis, microfluidics postdoctoral fellows, engineers, research assistants and visiting students, etc.
    , interested applicants should send their resumes by email to: tong.
    si@siat.
    ac.
    cn
    .

    Lab homepage: http://isynbio.
    siat.
    ac.
    cn/sitonglab/

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