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Cited by 1,301Microbial Community Ecology and PhysiologyAlgal biology and biofuel productionProtist diversity and phylogeny

The DOI matches its Crossref record; 248 of the 248 references it cites were found in a registry or an index.

Algae-bacteria interactions: Evolution, ecology and emerging applications

Open access
Ramanan, Rishiram, Kim, Byung-Hyuk, Cho, Dae-Hyun, Oh, Hee-Mock, Kim, Hee-Sik·2016·Biotechnology Advances
DOI 10.1016/j.biotechadv.2015.12.003
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Abstract

Algae and bacteria have coexisted ever since the early stages of evolution. This coevolution has revolutionized life on earth in many aspects. Algae and bacteria together influence ecosystems as varied as deep seas to lichens and represent all conceivable modes of interactions - from mutualism to parasitism. Several studies have shown that algae and bacteria synergistically affect each other's physiology and metabolism, a classic case being algae-roseobacter interaction. These interactions are ubiquitous and define the primary productivity in most ecosystems. In recent years, algae have received much attention for industrial exploitation but their interaction with bacteria is often considered a contamination during commercialization. A few recent studies have shown that bacteria not only enhance algal growth but also help in flocculation, both essential processes in algal biotechnology. Hence, there is a need to understand these interactions from an evolutionary and ecological standpoint, and integrate this understanding for industrial use. Here we reflect on the diversity of such relationships and their associated mechanisms, as well as the habitats that they mutually influence. This review also outlines the role of these interactions in key evolutionary events such as endosymbiosis, besides their ecological role in biogeochemical cycles. Finally, we focus on extending such studies on algal-bacterial interactions to various environmental and bio-technological applications.

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Crossref · 10.1016/j.biotechadv.2015.12.003

Cites

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Figures

Image 1
CC-BY-NC-ND · From the PDF
Fig. 1 A pictorial representation of evolution of algae after primary (PE) and secondary endosymbiosis (SE) events. The green branches indicate the green lineage while the red branches indicate the red lineage respectively. The dashed lines indicate the presence of sub-groups within the respective lineages where primary and/or secondary endosymbiosis is known to have occurred. The individual images used in this figure are only representative and some of these images are accessed through Creative Commons Attribution License.
Fig. 1 A pictorial representation of evolution of algae after primary (PE) and secondary endosymbiosis (SE) events. The green branches indicate the green lineage while the red branches indicate the red lineage respectively. The dashed lines indicate the presence of sub-groups within the respective lineages where primary and/or secondary endosymbiosis is known to have occurred. The individual images used in this figure are only representative and some of these images are accessed through Creative Commons Attribution License.CC-BY-NC-ND · From the PDF
Fig. 2 Confocal laser scanning images merged with differential interference contrast microscopic images of several multicellular algae and their closest unicellular relative. The strains were stained with SYBR green and pseudo-colored in yellow. The images reveal the presence of bacteria in all strains, including V. carteri (B), especially in flagellates and outer layers of ECM (A & B) whereas the gonidia do not have significant bacterial presence on their outer surface (C). The scale bar represents 5 μ m.
Fig. 2 Confocal laser scanning images merged with differential interference contrast microscopic images of several multicellular algae and their closest unicellular relative. The strains were stained with SYBR green and pseudo-colored in yellow. The images reveal the presence of bacteria in all strains, including V. carteri (B), especially in flagellates and outer layers of ECM (A & B) whereas the gonidia do not have significant bacterial presence on their outer surface (C). The scale bar represents 5 μ m.CC-BY-NC-ND · From the PDF
Fig. 3 The algal phycosphere and its components. Recoloured SEM images of axenic C. vulgaris (A) show the presence of cell sheath in dividing cells, whereas xenic C. vulgaris houses bacteria on the cell wall (white arrow) and beneath the cell sheath (red arrow) (B).
Fig. 3 The algal phycosphere and its components. Recoloured SEM images of axenic C. vulgaris (A) show the presence of cell sheath in dividing cells, whereas xenic C. vulgaris houses bacteria on the cell wall (white arrow) and beneath the cell sheath (red arrow) (B).CC-BY-NC-ND · From the PDF
Fig. 4 An illustration of components of algal -bacterial association in aquatic ecosystem and some proven mechanisms. All the mechanisms of exchange have been described in the text.
Fig. 4 An illustration of components of algal -bacterial association in aquatic ecosystem and some proven mechanisms. All the mechanisms of exchange have been described in the text.CC-BY-NC-ND · From the PDF
Fig. 5 Various applications of algal -bacterial interactions for biotechnology and environmental sectors.
Fig. 5 Various applications of algal -bacterial interactions for biotechnology and environmental sectors.CC-BY-NC-ND · From the PDF

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Citations

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Research works printed but not linked: 2

  1. Neale, 1987, Algal photoinhibition and photosynthesis in the aquatic environment, Photoinhibition, 9, 39
  2. Sachs, 2006, A shift to parasitism in the jellyfish symbiont Symbiodinium microadriaticum. Proceedings biological sciences/the royal, Society, 273, 425

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Metadata

Authors
Ramanan, R., Kim, B.-H., Cho, D.-H., Oh, H.-M., & Kim, H.-S.
Affiliations
Korea Research Institute of Bioscience and Biotechnology (KR)
Corresponding author
Kim, Hee-Sik
ORCID
Venue
Biotechnology Advances
Publisher
Elsevier BV
Published
2016-01
Volume
34
Issue
1
Pages
14-29
ISSN
0734-9750 (ISSN-L)
DOI
10.1016/j.biotechadv.2015.12.003
OpenAlex
W2188082055
Cited by
1,301
References
248
Citations by year
2026: 112 · 2025: 157 · 2024: 151 · 2023: 141 · 2022: 171 · 2021: 125 · 2020: 129 · 2019: 116 · 2018: 101 · 2017: 74 · 2016: 24
FWCI
6.10
Type
journal article
Language
en
Open access
Licence
Locations
  • Biotechnology Advances (publishedVersion, cc-by-nc-nd)
  • PubMed (publishedVersion)
  • KRIBB Repository (submittedVersion)
Funders
  • Advanced Biomass R&D Center (ABC) of Global Frontier Project (2015M3A6A2065697)
  • Korea Government Ministry of Oceans and Fisheries (20150184)
  • KRIBB Research Initiative Program
Topics
  • Physical Sciences › Environmental Science › Ecology › Microbial Community Ecology and Physiology
  • Physical Sciences › Energy › Renewable Energy, Sustainability and the Environment › Algal biology and biofuel production
  • Life Sciences › Agricultural and Biological Sciences › Ecology, Evolution, Behavior and Systematics › Protist diversity and phylogeny
Keywords
algal-bacterial interactions, coevolution, mutualism, parasitism, Roseobacter, endosymbiosis, primary productivity, biogeochemical cycles, algal biotechnology, flocculation, lichens, deep-sea ecosystems
MeSH terms
Phaeophyceae, Animals, Biodegradation, Environmental, Biotechnology, Biological Evolution, Host-Parasite Interactions, Lichens, Phytoplankton, Symbiosis, Ecosystem, Aquaculture, Bacterial Physiological Phenomena, Anthozoa, Microalgae

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