General Aspects/Case Studies on Sources and Bioremediation Mechanisms of Metal(loid)s 157
Table 9.2. Remediation of metal(loid)s by the combination of plants and microbial species.
Metals
Plant species
Microbial Species
Mechanism of removal
References
Zn
Brassica juncea
Pseudomonas
brassicacerarum,
Rhizobium leguminosarum
Organic acid secretion and
metal chelation enhancement by
phytochelatins
Adediran et al.
2015
Cicuta virosa
Rhodopseudomonas sp.,
Pseudomonas putida
Siderophores and indole-3
acetic acid production
Nagata et al. 2015
Ni
Alyssum
pintodasilvae
Arthrobacter
nicotinovorans
Siderophores and organic acid
production
Cabello-Conejo
et al. 2014
Helianthus
annuus
Pseudomonas libanensis
and Claroideoglomus
claroideum
Solubilization of phosphate,
ni phytostabilized by
exopolysaccharide (EPS)
Ma et al. 2019
Al
Miscanthus
sinensis
Chaetomium cupreum
Production of siderophore
(oosporein)
Haruma et al.
2019
Cd
Ocimum
ratissimum
Arthrobacter sp.
Production of EPS
Prapagdee and
Khonsue 2015
Zn, Cu and Pb
Clethra
barbinervis
Clethra barbinervis,
Rhizodermea veluwensis
Melanin and siderophore
production
Yamaji et al. 2016
Zn, Cd and Pb
Sedum
plumbizincicolaa
Endophytic bacterium E6S
Organic acid production,
Aminocyclopropane-1
carboxylate (ACC) and Indole
3-acetic acid (IAA) production,
phosphate solubilization,
Ma et al. 2016
As, Cd, Cu, Pb
and Zn
Miscanthus
sinensis
Pseudomonas koreensis
AGB-1
Aminocyclopropane-1
carboxylate (ACC) deaminase
Babu et al. 2015
Cr(VI), Fe,
Mn, Zn, Cd,
Cu and Ni
Vetiveria
zizanioides
Bacillus cereus
Production of IAA, ACC,
solubilize phosphate and
production of ACC
Nayak et al. 2018
Cd and Pb
Simplicillium
chinense
Phragmites communis
Pb bio sorption by EPS and Cd
chelate formation
Jin et al. 2019
Cd, Zn and Cu
Solanum nigrum
Pseudomonas sp. Lk9
Organic acids and siderophore
and biosurfactant production
Chen et al. 2014
Zn, Cd and Pb
Salix dasyclados
Streptomyces sp.
Siderophore production
Złoch et al. 2017
9.6 Case Studies on Bioremediation of Metal(oids)
9.6.1 Arsenic
Microorganisms have evolved arsenic defense systems because of arsenic’s ubiquitous presence in
the environment. The arsenic resilience operon’s existence (ars) encodes enzymes degradation of
arsenate in an exhaustive study undertaken in Leon, Spain (Mateos et al. 2006). It was noted that as
arsenate gains entry into the cell via specialized (Pst) or nonspecific (Pit) phosphate transporters, its
incorporation in phosphate-rich fluids or environments is lower. When C. glutamicum is cultivated
in a low-phosphate medium or when the concentration of phosphate is reduced by precipitation,
As(V) absorption increases, followed by disabling the three arsenite permease genes found in
C. glutamicum’s genome, arsenite outflow was minimized. C. glutamicum ArsB1-B2, a double
arsenite permease mutant, was particularly sensitive to arsenate and arsenite (Ordóñez et al. 2005).
Ordóñez et al. (2005) successfully created C. glutamicum strains using omics approaches that may
horde heavy metals outside the cell (as a biosorbent), similar to E. coli and Ralstonia eutropha
(Kotrba et al. 1999) and Ralstonia eutropha (Valls et al. 2000).