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production of siderophores, ammonia, HCN, enzymes and secondary
metabolites.
16,17
The plant growth promoting methylotrophs as single
bioinoculants or with co-inoculated as microbial consortium may be
use as bioinoculants/biofertilizers of biocontrol agents for enhanced
crops production and soil fertility for sustainable agriculture.
18–21
The different class α, β and γ–proteobacteria of methylotrophic
bacteria communities have been reported worldwide. The class
α-proteobacteria has been reported as most dominant followed
by β–proteobacteria. The novel methylotrophic microbes have
been isolated and characterized from different habitats worldwide
including Methylocella silvestris BL2T , Methylocella palustris KT,
Methyloferula stellata AR4T and Methylocapsa acidiphila B2T from
acidic soil;
22–25
Methylobacterium tarhaniae N4211T from arid soil;
26
Methylobacterium iners 5317S-33T and Methylobacterium aerolatum
5413S-11T from air sample;
27
Methylobacterium adhaesivum AR27T
and Methylobacterium isbiliense AR24T from drinking water;
28,29
Methylobacterium brachiatum B0021T, Methylobacterium gregans
002-074T, Methylobacterium komagatae 002-079T, Methylobacterium
persicinum 002-165T and Methylobacterium tardum RB677T
from freshwater sample;
30
Methylobacterium organophilum XX,
Methylotenera versatilis 301T and Methylotenera mobilis JLW8T from
lakes;
31–33
Methylobacterium brachythecii 99bT, Methylobacterium
cerastii C44, Methylobacterium gnaphalii 23eT, Methylobacterium
gossipiicola Gh-105T, Methylobacterium haplocladii 87eT,
Methylobacterium oxalidis 35aT, Methylobacterium phyllosphaerae
B27T, Methylobacterium phyllostachyos BL47T, Methylobacterium
platani PMB02T, Methylobacterium pseudosasicola BL36T,
Methylobacterium thuringiense C34T, Methylobacterium trifolii
TA73T, from leaf surface of diverse plants;
34–42
Methylobacterium
aminovorans TH-1, Methylobacterium goesingense iEII3,
Methylobacterium soli YIM 48816T, Methylobacterium suomiense,
F20T, Methylobacterium thiocyanatum, Methylobacterium variabile
GR3T, Methylopila capsulata IM1T, and Methylopila helvetica
VKMB-189 from soil samples
43–50
To understand the mechanisms of plant growth promotion and
genes involved in plant growth promotion there are many reports on
whole genome sequences of methylotrophic bacteria are available
at NCBI GenBank database (https://www.ncbi.nlm.nih.gov)
Methylobacterium populi BJ001, Methylobacterium extorquens CM4,
Methylobacterium nodulans ORS 2060, Methylobacterium aquaticum
MA-22A, Methylobacterium radiotolerans JCM 2831, Methyloferula
stellata AR4, Methylotenera mobilis JLW8, Methylotenera versatilis
301, Methylobacterium sp. AMS5, Methylotenera versatilis 301
Methylotenera mobilis JLW8, Methylovorus glucosetrophus
SIP3-4, Methylovorus glucosetrophus SIP3-4, Methylobacterium
mesophilicum SR1.6/6, and Methylobacterium indicum SE2.11
Plant-associated methylotrophs produce PGP phytohormones such
as auxins, gibberellins and cytokinin by Methylobacterium extorquens
IIWP-43, M. extorquens MP1, M. mesophilicum B-2143, M.
mesophilicum HHS1-36, M. mesophilicum IIWP-45, M. mesophilicum
NIAW1-41, M. phyllosphaerae HHS2-67, M. radiotolerans HHS1-45,
M. radiotolerans IHD-35 and M. zatmanii MS4. Many methylotrophs
has been reported to fx N2 e.g. Methylobacterium mesophilicum
B-2143, M. nodulans 2060T, and Methylobacterium sp. THD-3511,
51–
56
. A vast number methylotrophs with P-solubilizing ability have
been reported Methylobacillus arboreus Iva, M. extorquens G10,
M. extorquens IIWP-43, M. lusitanum MSF 32, M. mesophilicum
IIWP-45, M. mesophilicum NIAW1-41, M. radiotolerans IHD-35,
Methylopila musalis MUSA and Methylovorus menthalis MM.
2,6,13,57,58
Conclusion
The methylotrophic microbes from diverse sources have
potential applications in agriculture, industry and allied sectors. The
methylotrophic bacteria could be used for plant growth and soil health
for sustainable agriculture when inoculated as single or as consortium
under the natural as well as abiotic stress conditions.
Acknowledgements
The authors are grateful to Prof. Harcharan Singh Dhaliwal, Vice
Chancellor, Eternal University, Baru Sahib, Himachal Pradesh, India
for providing infra-structural facilities and constant encouragement.
J Appl Biotechnol Bioeng. 2018;5(6):342‒344. 342
© 2018 Yadav et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which
permits unrestricted use, distribution, and build upon your work non-commercially.
Biodiversity and biotechnological applications of
novel plant growth promoting methylotrophs
Volume 5 Issue 6 - 2018
Neelam Yadav,
1
Ajar Nath Yadav
2
1
Gopi Nath PG College,Veer Bahadur Singh Purvanchal
University, India
2
Department of Biotechnology, Akal College of Agriculture,
Eternal University, India
Correspondence: Ajar Nath Yadav, Department of
Biotechnology, Akal College of Agriculture, Eternal University,
Baru Sahib, India, Tel +91-9882545085, Fax: +911799276006,
Email
Received: November 07, 2018 | Published: November 20,
2018
Journal of Applied Biotechnology & Bioengineering
Editorial
Open Access
Editorial
Methylotrophic bacterial community is a very important group
of bacteria utilizing reduced carbon compounds. Methylotrophic
bacteria are well enough to survive in all types of environmental
conditions including acidic/alkaline habitats,
1–3
hyper saline,
4,5
drought,
6–8
low temperature
9–11
and high temperature.
6,12,13
The
methylotrophic microbes help plant for adaptation under diverse
unfavourable environmental conditions. The pink pigmented
facultative methylotrophic (PPFMs) bacteria is abundantly reported
as plant microbiomes (epiphytes, endophytes, rhizospheric).
11,13,14
The
methylotrophic microbes could be promote the plant growth and soil
health for sustainable agriculture directly by N2-fxation fxation;
P, K and Zn solubilization; production of Fe-chelating compounds;
production of PGP hormones such gibberellic acids, auxin and
cytokinin and ACC deaminase activities
6,11,13,15
or by in-directly by