Phylogenetic analysis of aerobic anoxygenic phototrophic bacteria and their relatives based on farnesyl pyrophosphate synthase gene

被引:1
|
作者
Feng Fuying [1 ,2 ]
Jiao Nianzhi [1 ]
Du Hailian [1 ]
Zeng Yonghui [1 ]
机构
[1] Xiamen Univ, State Key Lab Marine Environm Sci, Xiamen 361005, Peoples R China
[2] Innermongolia Agr Univ, Coll Life Sci, Hohhot 010018, Peoples R China
基金
中国国家自然科学基金;
关键词
aerobic anoxygenic phototrophic bacteria; farnesyl pyrophosphate synthase; phylogeny; anaerobic anoxygenic phototrophic bacteria; nonphototrophic bacteria; ISOPRENYL DIPHOSPHATE SYNTHASES; CODON USAGE; EVOLUTION; DIVERSITY; MECHANISM;
D O I
10.1007/s13131-010-0066-3
中图分类号
P7 [海洋学];
学科分类号
0707 ;
摘要
The study aims to reveal phylogenetic and evolutionary relationship between aerobic anoxygenic phototrophic bacteria (AAnPB) and their relatives, anaerobic anoxygenic phototrophic bacteria (AnAnPB) and nonphototrophic bacteria (NPB, which had high homology of 16S rDNA gene with AAnPB and fell into the same genus), and validate reliability and usefulness of farnesyl pyrophosphate synthase (FPPS) gene for the phylogenetic determination. FPPS genes with our modified primers and 16S rDNA genes with general primers, were amplified and sequenced or retrieved from GenBank database. In contrast to 16S rDNA gene phylogenetic tree, AAnPB were grouped into two clusters and one branch alone with no intermingling with NPB and AnAnPB in the tree constructed on FPPS. One branch of AAnPB, in both trees, was located closer to outgroup species than AnAnPB, which implicated that some AAnPB would be diverged earlier in FPPS evolutionary history than AnAnPB and NPB. Some AAnPB and NPB were closer located in both trees and this suggested that they were the closer relatives than AnAnPB. Combination codon usage in FPPS with phylogenetic analysis, the results indicates that FPPS gene and 16S rRNA gene have similar evolutionary pattern but the former seems to be more reliable and useful in determining the phylogenic and evolutionary relationship between AAnPB and their relatives. This is the first attempt to use a molecular marker beside 16S rRNA gene for studying the phylogeny of AAnPB, and the study may also be helpful in understanding the evolutionary relationship among phototrophic microbes and the trends of photosynthetic genes transfer.
引用
收藏
页码:82 / 89
页数:8
相关论文
共 50 条
  • [41] Soil Chemistry and Nutrients Influence the Distribution of Aerobic Anoxygenic Phototrophic Bacteria and Eukaryotic Phototrophic Microorganisms of Physical Soil Crusts at Different Elevations on the Tibetan Plateau
    Haijian Yang
    Chunxiang Hu
    Microbial Ecology, 2022, 83 : 100 - 113
  • [42] Cloning, Expression Characteristics of Farnesyl Pyrophosphate Synthase Gene from Platycodon grandiflorus and Functional Identification in Triterpenoid Synthesis
    Liu, Meiqi
    Wang, Zhen
    Qin, Chen
    Cao, Huiyan
    Kong, Lingyang
    Liu, Tingxia
    Jiang, Shan
    Ma, Lengleng
    Liu, Xiubo
    Ren, Weichao
    Ma, Wei
    JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2024, 72 (20) : 11429 - 11437
  • [43] Community structure of aerobic anoxygenic phototrophic bacteria in algae- and macrophyte-dominated areas in Taihu Lake, China
    Limei Shi
    Yuanfeng Cai
    Xiaoli Shi
    Min Zhang
    Qingfei Zeng
    Fanxiang Kong
    Ping Xu
    Journal of Oceanology and Limnology, 2022, 40 : 1855 - 1867
  • [44] Patterns in Abundance, Cell Size and Pigment Content of Aerobic Anoxygenic Phototrophic Bacteria along Environmental Gradients in Northern Lakes
    Fauteux, Lisa
    Cottrell, Matthew T.
    Kirchman, David L.
    Borrego, Carles M.
    Garcia-Chaves, Maria Carolina
    del Giorgio, Paul A.
    PLOS ONE, 2015, 10 (04):
  • [45] Growth and bacteriochlorophyll a formation in taxonomically diverse aerobic anoxygenic phototrophic bacteria in chemostat culture:: Influence of light regimen and starvation
    Biebl, Hanno
    Wagner-Doebler, Irene
    PROCESS BIOCHEMISTRY, 2006, 41 (10) : 2153 - 2159
  • [46] Rhodoferax-related pufM gene cluster dominates the aerobic anoxygenic phototrophic communities in German freshwater lakes
    Salka, Ivette
    Cuperova, Zuzana
    Masin, Michal
    Koblizek, Michal
    Grossart, Hans-Peter
    ENVIRONMENTAL MICROBIOLOGY, 2011, 13 (11) : 2865 - 2875
  • [47] Diel variations in frequency of dividing cells and abundance of aerobic anoxygenic phototrophic bacteria in a coral reef system of the South China Sea
    Liu, Rulong
    Zhang, Yao
    Jiao, Nianzhi
    AQUATIC MICROBIAL ECOLOGY, 2010, 58 (03) : 303 - 310
  • [48] Aerobic Anoxygenic Phototrophic Bacteria in the Marine Environments Revealed by Raman/Fluorescence-Guided Single-Cell Sorting and Targeted Metagenomics
    Xu, Lin
    Yue, Xiao-Lan
    Li, Hong-Zhe
    Jian, Shu-Ling
    Shu, Wen-Sheng
    Cui, Li
    Xu, Xue-Wei
    ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2024, 58 (16) : 7087 - 7098
  • [49] Molecular cloning and expression of Chimonanthus praecox farnesyl pyrophosphate synthase gene and its possible involvement in the biosynthesis of floral volatile sesquiterpenoids
    Xiang, Lin
    Zhao, Kaige
    Chen, Longqing
    PLANT PHYSIOLOGY AND BIOCHEMISTRY, 2010, 48 (10-11) : 845 - 850
  • [50] Contribution of aerobic anoxygenic phototrophic bacteria to total organic carbon pool in aquatic system of subtropical karst catchments, Southwest China: evidence from hydrochemical and microbiological study
    Li, Qiang
    Song, Ang
    Peng, Wenjie
    Jin, Zhenjiang
    Mueller, Werner E. G.
    Wang, Xiaohong
    FEMS MICROBIOLOGY ECOLOGY, 2017, 93 (06)