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Strategies for optimizing the scalable microbial synthesis of vivianite

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Vivianite (Fe3(PO4)2·8H2O) has been reported to form as a secondary mineralization product during the microbial reduction of phosphate-containing Fe(III) minerals [1 – 3]. The phosphate-rich nature of vivianite makes it a suitable sink for phosphorus, which is a scarce and irreplaceable resource, and a major contributor to eutrophication in surface water bodies. There is, therefore, interest in synthesizing vivianite by Fe(III) reducing bacteria such as Geobacter sulfurreducens and Shewanella putrefaciens, to treat phosphate-rich waters, recovering the phosphate for re-use in agriculture. In this study, factors including the presence and absence of phosphate and electron shuttle, the buffer system, pH, microbial load, and the type of Fe(III)-reducing bacteria that influence the formation of vivianite under laboratory batch systems have been investigated. The rate of Fe(II) production, and its interaction with the residual Fe(III) and other oxyanions (e.g., PO43-, CO32-) was found to be the main driving factor for secondary mineral formation. Magnetite was formed in treatments with zero phosphates whereas vivianite and green rust were formed in treatments containing phosphate. The rate and extent of Fe(III) bioreduction were higher in Shewanella putrefaciens than in Geobacter sulfurreducens. Vivianite and green rust were both identified as the dominant endpoints in treatments with Geobacter sulfurreducens and Shewanella putrefaciens. [1] Fredrickson, Zachara, Kennedy, Dong, Onstott, Hinman, & Li (1998). Geochimica et Cosmochimica Acta 62, 3239-3257.[2] O’Loughlin, Boyanov, Gorski, Scherer, & Kemner (2021). Minerals 11, 149[3] Zachara, Kukkadapu, Fredrickson, Gorby, & Smith (2002). Geomicrobiology Journal 19, 179–207. 
Title: Strategies for optimizing the scalable microbial synthesis of vivianite
Description:
Vivianite (Fe3(PO4)2·8H2O) has been reported to form as a secondary mineralization product during the microbial reduction of phosphate-containing Fe(III) minerals [1 – 3].
The phosphate-rich nature of vivianite makes it a suitable sink for phosphorus, which is a scarce and irreplaceable resource, and a major contributor to eutrophication in surface water bodies.
There is, therefore, interest in synthesizing vivianite by Fe(III) reducing bacteria such as Geobacter sulfurreducens and Shewanella putrefaciens, to treat phosphate-rich waters, recovering the phosphate for re-use in agriculture.
In this study, factors including the presence and absence of phosphate and electron shuttle, the buffer system, pH, microbial load, and the type of Fe(III)-reducing bacteria that influence the formation of vivianite under laboratory batch systems have been investigated.
The rate of Fe(II) production, and its interaction with the residual Fe(III) and other oxyanions (e.
g.
, PO43-, CO32-) was found to be the main driving factor for secondary mineral formation.
Magnetite was formed in treatments with zero phosphates whereas vivianite and green rust were formed in treatments containing phosphate.
The rate and extent of Fe(III) bioreduction were higher in Shewanella putrefaciens than in Geobacter sulfurreducens.
Vivianite and green rust were both identified as the dominant endpoints in treatments with Geobacter sulfurreducens and Shewanella putrefaciens.
 [1] Fredrickson, Zachara, Kennedy, Dong, Onstott, Hinman, & Li (1998).
Geochimica et Cosmochimica Acta 62, 3239-3257.
[2] O’Loughlin, Boyanov, Gorski, Scherer, & Kemner (2021).
Minerals 11, 149[3] Zachara, Kukkadapu, Fredrickson, Gorby, & Smith (2002).
Geomicrobiology Journal 19, 179–207.
 .

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