[9]WW FOOD WASTE TO BIOFERTILIZER

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International Journal of Food Microbiology 374 (2022) 109719

Contents lists available at ScienceDirect

International Journal of Food Microbiology


journal homepage: www.elsevier.com/locate/ijfoodmicro

Recent advances on organic biofertilizer production from anaerobic


fermentation of food waste: Overview
Mohammed Y. Areeshi
Medical Laboratory Technology Department, College of Applied Medical Sciences, Jazan University, Jazan 45142, Saudi Arabia
Research and Scientific Studies Unit, College of Nursing and Allied Health Sciences, Jazan University, Jazan 45142, Saudi Arabia

A R T I C L E I N F O A B S T R A C T

Keywords: Massive utilizations of chemical fertilizer in agriculture sector to improve the farming productivity have created
Food wastes increasing possibility of environmental damages. Severe human health issues, global warming, poor fertility and
Bio-fertilizer high cost of soil maintenance are the major side effects of the utilizations of inorganic fertilizers and needs
Fermentation
immediate attention. To overcome these issues, agriculture farming has been shifted towards the development of
Anaerobic microbial digestion
Value addition
organic fertilizers using natural bio-resources. Organic fertilizers have several advantages like low-cost, being
produced from the renewable resources and are highly efficient to improve the productivity of soil and agri­
culture product, rapidly. Additionally, bio-fertilizers not only increase the production, nutrients and organic
matter but also neutralize the harmful impacts caused by the chemical fertilizers due to the potential combi­
nation of the microorganisms with organic wastes. Food wastes have tremendous potential to enhance the
production of bio-fertilizers because these wastes are present in bio-degradable forms and may efficiently
accelerate the activity of the microbial metabolic. Thus, the present review summarizes an overview of the
production strategy of bio-fertilizers using the combination of food wastes and microorganisms. Further, in depth
discussion have been done about the microbial digestion of food wastes to produce biofertilizer along with
discussions about the possible mechanisms involved therein. Plant growth promoting microorganisms and their
mechanisms have been also analyzed in the present review along with the existing limitations and sustainable
future prospective.

1. Introduction 2005 (Pandey et al., 2016). Further, when global market is analyzed, it is
noticed that the Asia is the major contributor of food wastes by gener­
Worldwide growth in human population have resulted tremendous ating 278 million tonnes of food wastes and listed at the top position
increase in food demand and its supply, consequently huge amount of (Hamid et al., 2020). The reason behind such a huge production of food
food wastes are generated (Muralikrishna and Manickam, 2017). The wastes is the dependency of Human’s primary livelihoods on foods
Food and Agriculture Organization (FAO) defines food wastes as “Total which are preferably produced from the agriculture sector (Ahmad
occurred qualitative & quantitative food losses during the process of the et al., 2019). Additionally, if these food wastes are just dumped in to the
supply chain, which happens at the different stages like production, land fill are regarded as the municipal solid wastes (MSWs). These MSWs
post-harvesting, and processing” (FAO). Additionally, huge production have their own disadvantages & advantages both, for example, if these
of food wastes affects the significant loss of other necessary resources are discarded as such they cause environmental pollution by releasing
such as water, land, and energy. Further, it was predicted by the FAO toxic gases and create ground water contamination by attracting flies
that globally 1.3 billion tonnes of food wastes are produced on the over it (Shamsuddin et al., 2020). On the other hand, if these MSWs are
annual basis and this is counted as one-third of the total food being properly managed, these can be transformed into the compost and an­
produced worldwide (Satlewal et al., 2018). Moreover, it is estimated imal feeds as the value added products. Production of compost using
that the relative economic and population growth will enhance the food wastes has huge advantages in resolving numerous issues related to
generation of food wastes in coming 25 years specially predicted for the the environment as well as agriculture sector (Ariana and Candra,
Asian countries (Du et al., 2018). In addition, urban food wastes will be 2017). Being highly rich in organic and nutrient components, compost
approaching to nearly 138 million tonnes by 2025 when compared to developed from the food wastes have number of advantages, like it will

E-mail address: marishi@jazanu.edu.sa.

https://doi.org/10.1016/j.ijfoodmicro.2022.109719
Received 12 March 2022; Received in revised form 28 April 2022; Accepted 8 May 2022
Available online 13 May 2022
0168-1605/© 2022 Elsevier B.V. All rights reserved.
M.Y. Areeshi International Journal of Food Microbiology 374 (2022) 109719

be natural or organic in nature, easy to be processed, eco & biocom­ fast production; bio-fertilizers carries potential opportunity and offer
patible and grabs high amounts of nutrients (Begum et al., 2019). great promise to improve the global food security via increasing the
Moreover, composts transformed from these wastes are highly efficient agricultural yield, specifically in the countries like Africa and Asia,
to rejuvenate the fertility of soil, and hence are capable to improve the which cover together ~50% and 74% of the total land mass as well as
productivity of agricultural farming. Further, this organic compost also population worldwide, respectively (Dantroliya et al., 2022). Therefore,
contains a number of fermentative microbial colonies which may the objective of the present review is to explore the opportunity and
transform food wastes into the compost through the fermentation pro­ potentials of food wastes mediated organic bio-fertilizer production and
cess. Transformation of composting via natural process is one of the its applications in the agriculture sector for the eco-friendly farming for
major advantages, meanwhile being natural in nature; the crops devel­ sustainable future.
oped by using such compost are healthy and safe for human consump­
tion (Mahmud and Chong, 2021). 2. Bio-fertilizer: significance and role
Though, a numbers of commercial compost or bio-fertilizers are
available in the market, however it is difficult to achieve fast and steady Bio-fertilizers is the combination of living microorganisms and
degradation rate, and this is mainly due to the substrate variations organic resources wherein organic resources functions as the growth
physicochemical and environmental conditions changes (Duan et al., supports for the microorganisms and hence called to be living fertilizers
2019). Moreover, mass scale production and consumption of chemical (Singh et al., 2019). The organic and natural resources fulfill nutrients
fertilizers have resulted in poor soil quality and may cause serious requirements like nitrogen, phosphorus, and potassium from the organic
environmental pollution issues (Gunjal, 2019). On the other hand, uti­ resources which is supplemented to the fertilizer during the formation
lizations of food wastes to produce bio-fertilizers may accelerate the process (Soumare et al., 2020). These essential nutrients are present in
population of thermotolreant and thermophilic microbiomes, and this the environmental surroundings, and due to the microbial activities they
can help to achieve highest growth of plants via improving the fertility are transformed into the soil. These bio-fertilizers enhance the soil
of the soil (Lu et al., 2018). In addition, development of bio-fertilizer quality by improving its fertility, biodiversity and nutrient availability
may also provide socioeconomic and ecological advantages for all, (Md. Tahir et al., 2019). Bio-fertilizers are not the direct source of nu­
including environment, animal and human health. Based on the digested trients but it contains different combinations of microbes which support
raw materials used therein, bio-fertilizers are also produced in many the crops to develop or access the required nutrition from the environ­
types at low-cost (Mahami et al., 2019) [Fig. 1]. ment. The diversity of microorganisms include free living microbes,
Anaerobic digestion based bio-fertilizers contains huge microbial cyanobacteria and bacterial endophytes, having capability of coloniza­
combination along with different nutrient compositions which is tion in some section of the plant and develops some kinds of symbiotic
important for the soil fertility. Bacterial and fungal species such as relationship with the host plant (Truckell et al., 2019). These all plant
Pseudomonas, Klebsiella, Samonella, Penicillum, Shigella, Bacillus, growth promoting bacteria performs the same mechanisms during the
Bacteriodes and Aspergillus are found and have been explored in the promotion of the bacterial growth (dos Santos et al., 2020). As per the
production of bio-fertilizers (Owamah et al., 2014). For example, working mechanisms of microbes, these are divided into different cat­
Klebsiella and Clostridium spp. are the free living bacterial community egories, which include direct and indirect mechanisms. In case of direct
responsible for the nitrogen fixation, whereas Bacillus and Pseudomonas route, they directly promote the plants growth by performing some
spp. are known as the phosphate solubilizers (Mojumdar and Deka, modifications in the hormone levels or by fulfilling the nutrient re­
2019). Anaerobic digestion process of bio-fertilizers may improve the quirements. On the other hand, in case of indirect mechanism, it reduces
transformation of wastes into value addition in form of bio-fertilizers. inhibitory effects of different harmful microorganisms (Agrawal, 2015).
Being renewable, utilization of waste materials therein, low-cost and These bio-fertilizers include several microbes such as phosphate

Fig. 1. Graphic illustration of how agricultural wastes and their constituents, including biopolymers, can be used as biostimulants and biofertilizers. [Adopted from
(Puglia et al., 2021) open access (CCBY)].

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M.Y. Areeshi International Journal of Food Microbiology 374 (2022) 109719

solubilizing bacteria (Pseudomonas sp.), bacteria responsible for the 3. Food waste for bio-fertilizers production
nitrogen fixation (Azotobacter, Rhizobium), fungi and nitrogen fixing
cynobacteria (Anabaena). Some special types of strains such as cellulo­ Production of bio-fertilizers from food wastes via anaerobic digestion
lytic microbes and bacteria which produce phytohormone (auxin) are (AD) method is the most common and frequently applied process (Chen
also found in bio-fertilizers (Ritika and Utpal, 2014) [Fig. 2]. Such et al., 2012). In various uses of industrial production & application, bio-
proper and balanced combinations of the microbes perform the task of fertilizer is a common byproduct. Panuccio et al., and Tampio et al., used
enhancing the nutrition supply for plants which can be easily be food wastes via AD treatment and the bio-fertilizer generated consisted
accessed. Bio-fertilizers are renewable and cheap source of nutrition for of high level of nitrogen in both the studies (Panuccio et al., 2016;
plants. Ibiene et al., performed a test to observe the function of plant Tampio et al., 2016). Further in the study of Rigby and Smith, bio-
growth promoting bacteria on the tomato plant (Ibiene et al., 2012). fertilizers developed from the organic wastes have been tested, and
These bio-fertilizer contained species like Nitrobactor, Azotobactor as these authors found the highest nitrogen content ~11.3% in case of bio-
well as Nitrosomonas which was applied to the plant and the observation fertilizer generated from the food wastes (Rigby and Smith, 2013).
was recorded. After five days of the application reading were as follow: Additionally, content of phosphorus and potassium are also found to be
root length = 10.0 cm, steam width = 1.0 cm, plant height = 15.8 cm high in food wastes based bio-fertilizers. It has been concluded that
and internodes length = 3.8 cm whereas, in case of the normal plant: nutrient contents of the bio-fertilizer produced is mainly depends on the
root length = 6.1 cm, steam width = 0.5 cm, internodes length = 2.5 cm type of food wastes used for the production of bio-fertilizer (Rossi et al.,
and plant height = 11.0 cm were noticed (Ibiene et al., 2012). Reddy 2016). Additionally, co-digestion of these food wastes with the combi­
et al., setup an experiment to observe the development in tomato plant nation of other sources may support the adjustment of C/N ratio which is
by using plant growth promoting Rhizo bacteria (Reddy et al., 2018). In necessary for the smooth running of the AD system. However, quality
these samples two species of Azospirillum and Azotobactor were used control maintenance of the food wastes during bio-fertilizer production
and the observations were recorded after 60, 45 and 30 days. The is mandatory to handle, and can be categorized into three category
maximum growth of plant height 51 cm, leaf area 59 cm square, namely physical, chemical and biological impurities which can be
germination 90% and branches per plant 8.66 were observed in the rectify by using different pretreatment methods. Additionally, pre­
samples (Reddy et al., 2018). Similarly, Alhia performed the experiment treatment is also essential to remove the heavy metals like impurities
using the greenhouse condition in which Azotobactor Chrococcum was during the production of bio-fertilizers (Mao et al., 2015). In a study
used for the nitrogen fixation on the cucumber plant (Alhia, 2010). In reported by Abdullah et al., authors found presence of heavy metals and
this experiment seven different treatments were given to 210 seeds to their high concentration beyond the permissible limit for bio-fertilizers,
cucumber plant and the observation was recorded after the three month. which if not treated may enter into the food chain and thus may create
It was noticed that the production was increased by 6.0% in the seeds harmful impact on living organism (Abdullah and Greetham, 2016).
which was inoculated by A. chroococcum as compared to the other Further, like AD system, frequently food wastes are combined with
samples. The inoculated plant also shows increment in weight of wet the farm wastes for the production of bio-fertilizer. These farm wastes
root by 18%, weight of dry roots by 31%, weight of wet plant as a whole commonly include cellulosic and lignocellulosic wastes and fulfill
by 13%, number of leafs and branches by 27% and the weight of dry nutrient requirements along with facilitating C/N ratio adjustment (Ma
plant as a whole by 11% (Alhia, 2010). Flores-Félix et al., isolated the et al., 2017). During the process of co-composting utilizations of food
Rhizobium leguminosarum strain using Phaseolus vulgaris nodules and wastes with the combination of farm wastes, moisture adjustment is the
observed its effect on the plant growth (Flores-Félix et al., 2013). This key factor to be optimized to avoid any contamination during the pro­
strain produces indole acetic acid and siderophores as well as it solu­ duction of bio-fertilizer. In the study of Tsai et al., bio-fertilizer was
bilizes phosphate content. Strain colonizes the root into two different produced via co-composting of food and farm wastes (Tsai et al., 2007).
horticultural crops, Daucus carota L. and Lactuca sativa L. This Rhizobium Along with AD and co-composting of farm wastes, solid state fermen­
leguminosarum strain promotes growth of both types of species of plants tation technology is also opted for the production of bio-fertilizers using
by increasing the uptake of nitrogen and phosphorous (Flores-Félix different food wastes. Along with composting, utilizations of different
et al., 2013). Apart from the microbes, it also contains biodegradable biomass will also work as carriers to support the production of bio-
wastes which acts as a carrier for such microorganisms. These carriers fertilizers (Uçkun Kiran et al., 2014). In support to bio-fertilizer pro­
can be lignite powder, bagasse, rice bran, peat, clay, wheat straw duction, different types of biodegradable wastes can be used as a carrier
compost, press mud, wheat bran, phosphate pellets or the combination for soil inoculants and for being a good carrier of these inoculants the
of such samples which can provide longer life-time to active microbes size of biomass should not exceed to the value of 40 μm (Phua Choo Kwai
which can facilitates crops by direct induction (Chaudhary et al., 2020). et al., 2009). The biomass can be a good carrier having properties like

Fig. 2. A simple diagram of the main technologies used for the conversion of organic waste into biofertilizer. [Adopted with permission from (Du et al., 2020)].

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M.Y. Areeshi International Journal of Food Microbiology 374 (2022) 109719

high absorbing capacity of moisture, nontoxic nature towards the mi­ phosphate solubilization and siderophore (Baghaee Ravari and Hei­
croorganisms, and can be easily autoclaved or sterilized, easy to process darzadeh, 2014).
and low-cost advantage (Senoo et al., 2002). Zhang et al., used maize Further, normal plant growth and stress tolerance are also affected
bran residue for carrying two different phosphate solubilizing Bacillus by the availability of ethylene hormone (Olanrewaju et al., 2017).
subtilis strains (Zhang et al., 2019). In these experiment highest soluble Different factors like gravity, temperature, nutrition, light, various
phosphorous was found to be 642.7 ± 0.43 mg/L. The optimum climatic stages of abiotic/biotic stress and plant hormones significantly affect the
conditions for these experiments were temperature 31 ◦ C, pH 7.0 and synthesis of ethylene in a particular plant. Various stresses such as excess
the content of water was 160% with filing capacity of 500 g/L. This bio- of light and water, availability of metals, high temperature, chemicals,
fertilizer showed improvement in the growth of wheat and Chinese ultra-violet lights, bacterial and fungal pathogens, cuts, nematode
cabbage which was analyzed on the basis of the height (approx 18.36%) damage and insects may cause enhancement of ethylene in plants (Glick,
as well as roots (approx. 34.03% and 27.22% individually) (Zhang et al., 2005, 2014). Additionally, production of ethylene more than the opti­
2019). Nurfalah et al., prepared three different combinations of carriers mum value is might be due to the action of aminocyclopropane-1-
using compost and rice bran for carrying most common fungal species carboxylate (ACC) oxidase enzymes in the tissues of the targeted
Trichoderma (Nurfalah et al., 2019). The ratio of rice bran and the plants and may affect the development of both shoot and root by
compost were 3:1, 2:2 and 1:3 and mixed with microbes. The entire reducing its health. This critical situation can be alleviate and restore
sample was observed during 30, 15 and 7 days after the preparation of with the proper improvements and growth in the crops by colonizing
the mixture and it was found that the combination of carrier with 1:3 ethylene stress of plant rhizosphere with the help of ACC deaminase
ratios was the optimum for producing tomatoes (Nurfalah et al., 2019). which produces plant growth promoting (PGP) bacteria (Singh et al.,
If the carrier have all the necessary requirements and take the re­ 2015). The major application of ACC deaminase which contains PGP
sponsibility of the carried microorganisms then it will act as a desirable bacteria generally reduces the concentration of ethylene produced by
and demandable substrate for bio-fertilizer production. the various stresses which results the decrement in the damage caused
by the different fungal and bacterial pathogen (Nadeem et al., 2010).
4. Mechanism of bio-fertilizer This ACC deaminase converts the ACC available across the root into
ammonia and α-ketobutyrate, along with these it also checks the pro­
4.1. Plant growth promotion by bio-fertilizers using direct mechanisms duction of ethylene which creates problem for the plant growth pro­
moting bacteria. The plants which is subjected by the ACC deaminase
This mechanism of the plant growth promotion includes supply of shows better growth due the less ethylene and also shows good resis­
useful nutrients and hormones to the crops for increasing the produc­ tance towards the various stresses (Karthikeyan et al., 2012). The plant
tivity and the growth in the crops. It includes a number of activities like growth promoting bacteria which contain ACC deaminase attracts the
production of auxin, nitrogen fixation, solubilization of the both po­ attention of researchers. These bacteria promote the plant growth in any
tassium and phosphate, providing support in the development of plants condition whether it is under the stress or not, along with this different
nodule as well as production of phytohormone (Vejan et al., 2016). genetic manipulation of cultivars with genes are the main reason of the
Production of auxin is one of the most likely and predominantly used scientific attention (Saleem et al., 2007).
techniques generally used for explaining the beneficial effect of plant However, this technique is found to be highly effective on different
growth by producing more bacterial growth for the developments of types of pathogens and results are limited at batch scale investigation in
crops. Auxin is generally released as a secondary metabolite when about greenhouse condition. Madhaiyan et al., observed the activity of
80% of rhizoshpere is synthesized. Maximum auxin are developed using methylo-bacterium which increases the concentration of indo-3-acetic
amino acids tryptophan found in the roots of the crops and depending acid that further increases the ACC activity (Madhaiyan et al., 2007).
upon the plants genotype its concentration also varies (Leaungvutiviroj In this experiment, concentration of ACC was measured in the root of
et al., 2010). Auxins are generally synthesized by minimum three canola which was the targeted plants and different growth regulators
different biosynthetic ways. These pathways are as follows: the indole and action of methylo-bacterium was investigated. It was also observed
acetamide route, indole pyriuvic acid route and indole acetoitrile/ace­ that the inoculation of this strain with different growth inhibitory con­
taldoxime route (Hakim et al., 2018). It was found that different plant centration of many growth regulators may harm the targeted crops.
growth promoting bacteria have followed one, two or even three of these Further, nitrogen is one of the most required nutrients for the
biosynthetic pathways for the synthesis of auxin. Plants show sensi­ effective fertility of the soil, increasing crops productivity and proper
tiveness at different stages towards different auxin levels (Zhao, 2010). growth of plants. Since, plants cannot use directly available nitrogen
As per the behavior, the optimum amount of auxin which acts effectively from the atmosphere, hence converted into ammonia via biological ni­
in promoting the growth in the crops it is near about the value having trogen fixation process by means of nitrogenase activity of the micro­
five orders higher for shoot as compared to roots. Moreover, the effect on organisms (Fatima et al., 2019; Leghari et al., 2016). Rhizobia is known
the inhibition or stimulation of plant growth is defined by the amount of as a potential nitrogen fixer while in case of free living bacteria, utili­
auxin developed in the plant. The concentration of plants auxin is either zation frequency for nitrogen production is low because they fix less
optimal or suboptimal; therefore the hormonal level can be changed to amount of nitrogen. Ravikumar et al., collected 44 different samples
supra-optimal or optimal with the addition of bacterial auxin (Besseau from the mangrove habitat of southeast coast of India wherein Azo­
et al., 2007). Ahmed and Hasnain, isolated two strain plant growth bacter species were found to be emerging as the dominating bacterial
promoting bacteria which produces auxin and identified as Bacillus community for nitrogen fixation (Ravikumar et al., 2004). Additionally,
species (Ahmed and Hasnain, 2010). The optimum climatic condition due to the considerable N2 fixation, noticeable changes in the plant
for the maximum production was found to be 37 ◦ C after 48 h of incu­ growth was also observed such as length of the roots got increased by
bation. It was also observed that this auxin producing strain showed 48.45%, shoot biomass by 29.49%, root biomass by 98.2% and the area
similar retention time as indole-3-acetic acid. This strain was further of leaf by 277.86% (Ravikumar et al., 2004). Tilak et al., performed the
inoculated with solanum tuberosum sprouts and the observations were glasshouse experiment on pigeonpea by applying the combination of
recorded on the basis of the growth and development. The increment in plant growth promoting bacteria like Rhizobium sp. Azotobactor chroo­
shoot was observed which is about 35% to 40% and number as well as coccum and Pseudomonas fluorescens (Tilak et al., 2006). Based on
length of the roots also were found to be increased. In a study, Baghaee different microbial species selected therein, growth, length and weight
Ravari and Heidarzadeh performed an experiment on the plant growth of plants were found to be completely different (Tilak et al., 2006).
promoting bacteria and isolated thirty five different strains in which six Microorganisms by which phosphorus are solubilized are described
strains were reported for the potential auxin production along with as phosphate solubilizing microorganisms. These microorganisms are

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M.Y. Areeshi International Journal of Food Microbiology 374 (2022) 109719

not deleterious to the environment as well as provide phosphate to the (Dimkpa et al., 2008). The production of three different kinds of
plants in more simple and acceptable forms. They are capable of con­ hydroxamate siderophores were observed with the help of electro-spray
verting both organic as well as inorganic types of insoluble phosphate to ionization mass spectrometry. The experiment was performed in pres­
the simple compounds which will be relatively be easier for the plants to ence and absence of siderophores on the cowpea and increment in the
utilize (Walia et al., 2017). The activities of phosphate solubilizers can height and biomass were observed in the targeted plant despite of the
be affected by many factors such as environment, soil and plants con­ iron and nickel stress. This nickel resistive streptomyces acidiscabies
ditions, fungal and bacterial strains. Application of minerals dissolving E13 plays a dual role by providing iron to the targeted plant as well as
substance such as ions of hydroxyl groups, organic acids, CO2 and pro­ offers protection against the toxicity of nickel (Dimkpa et al., 2008).
tons are the main mechanism of solubilizing inorganic phosphate Radziki et al., performed the investigation of siderophores produced by
(Jakobsen et al., 2005). Production of phosphates takes place when the bacterial strain and tested on tomato plant, and this increases the
liberation of organic acids along with their hydroxyl ions chelate cations chlorophyll content, plant production and content of iron (Radzki et al.,
and carboxyl ions or reduction in pH occurs. Whereas, about 30% to 2013). Siderophers produced from the chryseo bacterium c138 strain
50% of organic phosphorus is available in the form of inositol hex­ could function as an effective source of iron supply to iron starved to­
aphosphate, commonly known as Phytate (Bashan et al., 2013). mato plants (Radzki et al., 2013) [Fig. 3].
The breaking down of this phytate is possible because of the phytase
enzyme but it is produced in very small quantity by the roots of the
4.2. Indirect mechanism of promoting plant growth using organic fertilizer
plants. However, many plant growth promoting bacteria are capable of
solubilizing phytate. Park et al., isolated Pseudomonas flurorescens
The nature of plant growth promoter (PGP) bacteria is to support the
RAF15 from ginseng rhizosphere to study the mechanism of phosphate
developments in the crops by replacing the use of insecticides as a bio-
solubilization using two different mechanism; organic acid production
control agent (Lehman et al., 2011; Radzki et al., 2013; Svircev et al.,
and extraction of proton by ammonium assimilation (Park et al., 2009).
2011). The production of plants was reduced by 10% every year in
Nevertheless, these authors did not find any difference in phosphate
countries like USA, UK, Brazil whereas, in the countries like India,
solubilization and pH change (Park et al., 2009). In one of the studies,
China, Japan it rises up to 20% per year just because of the different
Ouyabe et al., observed the response of non-native plant growth pro­
plant diseases (Chakraborty and Newton, 2011). In order to reduce the
moting bacteria on rice plant under the greenhouse conditions and
massive application of inorganic fertilizers and insecticides many eco-
recorded enhancement in the nitrogen and phosphorous solubilization
friendly, PGP bacteria are still at the development stage whereas some
after fourteen days (Ouyabe et al., 2020).
of them are already available at the commercial level.
Next, siderophores are the iron chelators and perform the role of iron
A plant growth promotion bacterium produces one or more than one
carrier and shows high affinity towards the specific ligands. They belong
antibiotics in order to neutralize the harmful effects of phytopathogens.
to the group of peptide molecules of small in size having functional
The antibiotic which was selected for the neutralization of the specific
group along with a side chains. Microorganism which produces side­
pathogen shows positive response against some of the other pathogen,
rophore reduces the proliferation of pathogens by minimizing the
and there is a variation in the action of these antibiotics developed using
quantity of iron available to the pathogens (Crumbliss and Harrington,
the plant growth promotion bacterium at different field conditions
2009). Plant growths promoting bacteria which produce siderophores
(Molina et al., 2003). The performance as well as the action can be
minimizes the proliferation of phyto-pathogens by librating side­
changed by these bio-control microorganisms by performing variation in
rophores and are having very high affinity towards the iron element. It
the methodology of formulation and cultivation of the bio-control PGP
holdup most of the ferric ions which are available inside the rhizosphere
bacteria in the laboratory (Vurukonda et al., 2018). Many antibiotics are
of the host crops and protects the host plant from different bacterial and
developed from the microorganisms of the genera Pseudomonas and
fungal pathogen, whereas the bio-control plant growth promoting bac­
Bacillus. A lots of metabolites are produced which act as antibacterial,
teria are bound from utilizing enough iron for their growth (Garénaux
antifungal, antiviral, antihelmintic, antioxidant, phytotoxic, antimicro­
et al., 2011). Thus, lack of the iron content causes the loosing ability to
bial, antitumor and cytotoix agents (Stan et al., 2021). Bacillus is pro­
perform the task of anti-pathogen activity because they are unable to
duced from the strains such as non-ribosomal peptide, ribosome and
proliferate. Dimkpa et al., reported production of hydroxamate side­
ployketide synthetases. Application of different plant pathogens in place
rophores with the help of nickel resistive streptomyces acidiscabies E13
of chemical pesticides such as Pseudomonas sp. and Bacillus sp. play an

Fig. 3. A schematic descriptive mechanism of various traits shown by Plant Growth-Promoting Microbes present in biofertilizers that acts as bioinoculants and
promote plant growth. [Adopted from (Mahmud and Chong, 2021) (CC BY-NC-ND license)].

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M.Y. Areeshi International Journal of Food Microbiology 374 (2022) 109719

important role by producing antibiotics. Antibiotics produced by for the plants but unable to fulfill the complete demand of the host plant
different plant growth promoting bacteria are one of the most studied that’s why it cannot replace other fertilizers. Effectiveness and the
bio-control technique employed from past few years. Pseudomonas functional stability of bio-fertilizers are also affected with the changes in
species generates different types of antifungal antibiotics such as pyr­ the environmental parameters like pH, moisture, carrier type of the soil
rolnitrin, cepaciamide A, and phenazines, antitumor antibiotics such as and unavailability of the efficient strains that help to develop bio-
cepafungins and FR901463. It also produces bacterial antibiotics, anti­ fertilizer (Ritika and Utpal, 2014).
viral antibiotics, and Bacillus sp. also produces many antifungal and The present review provides an overview of the production process
antibacterial antibiotics. Some of these Bacillus produced species are of organic fertilizers from the food wastes via microbial fermentation
lipopetide antibiotics, bacillomycin, iturins and surfactins. These anti­ and analyzed the recent advancement in this area. As per the contents
biotics are classified into two different categories on the basis of its expressed in the review, the availability and value addition possibility of
volatile nature. A Volatile antibiotic includes hydrogen cyanide, ke­ the food wastes have been explored. Additionally, microbial mecha­
tones, alcohols’etc., whereas non volatile antibiotics include antibiotics nisms of bio-fertilizers to promote plants growth have been explained in
like aminopolyols, phenylpyrrole and lipopeptides etc. detail through the direct and in-direct mechanisms. Direct mechanism of
Plants generally promote growth of many microorganisms which are working of bio-fertilizers promotes the plant growth by providing
responsible for degrading the cell wall when they get infected by the various nutrients such as vitamins, protein and minerals etc. These bio-
fungal phyto-pathogens. These microorganisms contain chitinase which fertilizers also induce plants development via enhancing growth of
breakdown chitin, which is the cell wall of the lots of phyto-pathogens hormones such as auxin production, nitrogen fixation, solubilization of
and residue product of β-(1, 4)-N-acetyl glucosamine polymer (Oye­ the both potassium and phosphate etc. On the other hand, indirect
leye and Normi, 2018). Up to some level, fungal cells can also acts as a mechanism supports to improve the immunity against the pathogens.
protease which degrade the proteins of the cell wall and lipase, and is Moreover, these food wastes either alone or in some ratio with two or
responsible for the degradation of lipids. Apart from the plant encoded more food wastes may enhance the biodegradability and acts as a carrier
enzymes for the degradation of cell, few bio-control plant growth pro­ support for the organic bio-fertilizers development. In addition, appli­
moting bacteria produces same types of enzymes which is responsible cation of these types of bio-fertilizers which can be developed from the
for the cell wall degradation (Mondal et al., 2016). Plant growth pro­ food wastes may greatly help to reduce the demand of insecticides and
motion bacterium strains when transferred genetically with the genes of pesticides, efficiently and can help to maintain the long term sustain­
cell wall degrading microorganisms perform with higher efficiency. ability of the environment.
Gruber and Seidl-Seiboth, described about the Glycoside hydrolase
family 18 which includes about all types of fungal chitinases that are CRediT authorship contribution statement
involved in the cell wall degradation (Gruber and Seidl-Seiboth, 2012).
The role of these cell wall degrading enzymes and chitinases apart from Mohammed Yahya Areeshi: Conceptualization, Writing – review &
the cell wall degradation is the recycling of the cell wall of its own editing.
fungus and its remodeling too. On the basis of the amino acid sequences,
the chitinases from Glycoside hydrolase family 18 are classified in to
three different categories A, B and C. The subgroup A and C are exo- Declaration of competing interest
chitinases which degrade terminals of the chitin chains and produces
oilgomers or dimmers of acetyl-glucosamine. Whereas, sub-group-B is Author of the manuscript declare there is no conflict of interests.
supposed to be endo-chitinases which degrades reducing and non-
reducing ends of chitin chain. Thereafter, the released dimer-
References
chitobiose is degraded into two different monomers of N-acetyl-gluco­
saminidases, NAG1 and NAG2. Wherein, NAG1 is released in to the Abdullah, J., Greetham, D., 2016. Optimizing cellulase production from municipal solid
medium whereas the NAG2 is attached to the cell wall of Tricoderma waste (MSW) using solid state fermentation (SSF). J. Fundam. Renew. Energy Appl.
06.
(Gruber and Seidl-Seiboth, 2012).
Agrawal, P., 2015. Plant growth promoting rhizobacteria: mechanism and current
Some special type of bacterial phytopathogens gets degraded using prospective. J. Fertil. Pestic. 6, 1–9.
some specific types of bacteriophages and bacterial viruses. In order to Ahmad, F.B., Zhang, Z., Doherty, W.O.S., O’Hara, I.M., 2019. The outlook of the
attend this technique, firstly proper identification of those particular production of advanced fuels and chemicals from integrated oil palm biomass
biorefinery. Renew. Sustain. Energy Rev. 109, 386–411.
phyto-pathogens must be done, and after this isolation and character­ Ahmed, A., Hasnain, S., 2010. Auxin-producing Bacillus sp.: auxin quantification and
ization of that specific strain should be performed. Subsequently, the effect on the growth of Solanum tuberosum. Pure Appl. Chem. 82, 313–319.
characterization process, identification of such phytopathogen must be Alhia, B.M.H., 2010. The Effect of Azotobacter chrococcum as Nitrogen biofertilizer on
the Growth And Yield of Cucumis sativus.
done which can lyse the specific pathogen without harming other useful Ariana, A., Candra, K.P., 2017. Isolation and characterization of lignocellulolytic
microbes (Armon, 2020). These bacteriophages are sprayed over the microbes from oil palm empty fruit bunches (EFB). SustinereJ.Environ.Sustain. 1,
plant which is infected by the bacterial phytopathogen, and the mixture 1–9.
Armon, R., 2020. Bacteriophage application and biological safety (or how should I train
is the combination of two or more sample of bacteriophage strains which my dog not to bite me). In: Witzany, G. (Ed.), Biocommunication of Phages. Springer
are specific for lyse of phytopathogens (Frampton et al., 2012). These International Publishing, Cham, pp. 309–333.
mixtures reduce the possibility of the development of resistive nature Baghaee Ravari, S., Heidarzadeh, N., 2014. Isolation and characterization of rhizosphere
auxin producing Bacilli and evaluation of their potency on wheat growth
towards the strains in the phytopathogens due to the presence of many
improvement. Arch. Agron. Soil Sci. 60, 895–905.
binding sites of various areas on the surfaces of pathogens. Bashan, Y., Kamnev, A.A., de-Bashan, L.E., 2013. Tricalcium phosphate is inappropriate
as a universal selection factor for isolating and testing phosphate-solubilizing
bacteria that enhance plant growth: a proposal for an alternative procedure. Biol.
5. Limitations and conclusions Fertil. Soils 49, 465–479.
Begum, H., Alam, A.S.A.F., Awang, A., 2019. Sustainability of Malaysian oil palm: a
Though bio-fertilizers have lots of advantage, a number of drawbacks critical review. Int.J.Environ.Sustain.Dev. 18, 409–429.
Besseau, S.b., Hoffmann, L., Geoffroy, P., Lapierre, C., Pollet, B., Legrand, M., 2007. Plant
are also associated with these fertilizers in terms of certain limitations
Cell 19, 148–162.
such as, it requires extra care to survive for the long duration and must Carvajal-Muñoz, J., Carmona García, C., 2012. Benefits and limitations of biofertilization
be applied before the expiry date (Naveed et al., 2014). It is also possible in agricultural practices. In: Livest.Res.Rural Dev.. Livest. Res. Rural Dev., 24.
that inoculants can even harm the carrier and there is also a possibility of Chakraborty, S., Newton, A.C., 2011. Climate change, plant diseases and food security:
an overview. Plant Pathol. 60, 2–14.
unwanted inoculants to be grown which reduces the fertility of the soil Chaudhary, P., Mitra, D., Pracheta, D., Mohapatra, P., 2020. In: Assessment of Different
(Carvajal-Muñoz and Carmona García, 2012). Bio-fertilizers are useful Carriers Materials for Bio-fertilizers And Their Effect on Plant Growth, pp. 27–50.

6
M.Y. Areeshi International Journal of Food Microbiology 374 (2022) 109719

Chen, L., Zhao, L., Ren, C., Wang, F., 2012. The progress and prospects of rural biogas Mao, C., Feng, Y., Wang, X., Ren, G., 2015. Review on research achievements of biogas
production in China. Energy Policy 51, 58–63. from anaerobic digestion. Renew. Sustain. Energy Rev. 45, 540–555.
Crumbliss, A.L., Harrington, J.M., 2009. Iron sequestration by small molecules: Md P., Tahir, Liew, W.-P.-P., Lee, S.Y., Ang, A.F., Lee, S.H., Mohamed, R., Halis, R., 2019.
thermodynamic and kinetic studies of natural siderophores and synthetic model Diversity and characterization of lignocellulolytic fungi isolated from oil palm empty
compounds. In: van Eldik, R., Hubbard, C.D. (Eds.), Advances in Inorganic fruit bunch, and identification of influencing factors of natural composting process.
Chemistry. Academic Press, pp. 179–250. Waste Manag. 100, 128–137.
Dantroliya, S., Joshi, C., Mohapatra, A., Shah, D., Bhargava, P., Bhanushali, S., Mojumdar, A., Deka, J., 2019. Recycling agro-industrial waste to produce amylase and
Pandit, R., Joshi, C., Joshi, M., 2022. Creating wealth from waste: an approach for characterizing amylase–gold nanoparticle composite. Int. J. Recycl. Org. Waste
converting organic waste in to value-added products using microbial consortia. Agric. 8.
Environ.Technol.Innov. 25, 102092. Molina, L., Constantinescu, F., Michel, L., Reimmann, C., Duffy, B., Défago, G., 2003.
Dimkpa, C., Svatos, A., Merten, D., Büchel, G., Kothe, E., 2008. Hydroxamate Degradation of pathogen quorum-sensing molecules by soil bacteria: a preventive
siderophores produced by Streptomyces acidiscabies E13 bind nickel and promote and curative biological control mechanism. FEMS Microbiol. Ecol. 45, 71–81.
growth in cowpea (Vigna unguiculata L.) under nickel stress. Can. J. Microbiol. 54, Mondal, S., Baksi, S., Koris, A., Vatai, G., 2016. Journey of enzymes in entomopathogenic
163–172. fungi. Pac.Sci.Rev.ANat.Sci.Eng. 18, 85–99.
dos Santos, R.M., Diaz, P.A.E., Lobo, L.L.B., Rigobelo, E.C., 2020. Use of plant growth- Muralikrishna, I.V., Manickam, V., 2017. Chapter sixteen - solid waste management. In:
promoting rhizobacteria in maize and sugarcane: characteristics and applications. In: Muralikrishna, I.V., Manickam, V. (Eds.), Environmental Management. Butterworth-
Front.Sustain.Food Syst.4. Front. Sustain. Food Syst., 4. Heinemann, pp. 431–462.
Du, C., Abdullah, J.J., Greetham, D., Fu, D., Yu, M., Ren, L., Li, S., Lu, D., 2018. Nadeem, S., Zahir, Z., Naveed, M., Ashraf, A., 2010. Microbial ACC-deaminase: prospects
Valorization of food waste into biofertiliser and its field application. J. Clean. Prod. and applications for inducing salt tolerance in plants. Crit. Rev. Plant Sci. 29,
187, 273–284. 360–393.
Du, C., Munir, S., Abad, R., Lu, D., 2020. Chapter 7 - valorization of organic waste into Naveed, M., Mehboob, I., Shakir, M., Hussain, M.B., Farooq, M., 2014. Biofertilizers in
biofertilizer and its field application. In: Bhaskar, T., Pandey, A., Rene, E.R., Pakistan: initiatives and limitations. Int. J. Agric. Biol. 17.
Tsang, D.C.W. (Eds.), Waste Biorefinery. Elsevier, pp. 179–198. Nurfalah, A., Ayuningrum, N., Affandi, M., Hastuti, L., 2019. Promoting growth of
Duan, Y., Awasthi, S.K., Liu, T., Verma, S., Wang, Q., Chen, H., Ren, X., Zhang, Z., tomato (Solanum lycopersicum L.) by using trichoderma –compost–rice bran based
Awasthi, M.K., 2019. Positive impact of biochar alone and combined with bacterial biofertilizer. IOP Conf.Ser.EarthEnviron.Sci. 305, 012074.
consortium amendment on improvement of bacterial community during cow manure Olanrewaju, O.S., Glick, B.R., Babalola, O.O., 2017. Mechanisms of action of plant
composting. Bioresour. Technol. 280, 79–87. growth promoting bacteria. World J. Microbiol. Biotechnol. 33, 197.
Fatima, P., Mishra, A., Saha, H., Kumar, P., 2019. In: Free Living Nitrogen Fixation And Ouyabe, M., Irie, K., Tanaka, N., Kikuno, H., Pachakkil, B., Shiwachi, H., 2020. Response
Their Response to Agricultural Crops, pp. 173–200. of upland rice (Oryza sativa L.) inoculated with non-native plant growth-promoting
Flores-Félix, J.D., Menéndez, E., Rivera, L.P., Marcos-García, M., Martínez-Hidalgo, P., bacteria. Agronomy 10, 903.
Mateos, P.F., Martínez-Molina, E., Velázquez, M.d.l.E., García-Fraile, P., Rivas, R., Owamah, H.I., Dahunsi, S.O., Oranusi, U.S., Alfa, M.I., 2014. Fertilizer and sanitary
2013. Use of Rhizobium leguminosarum as a potential biofertilizer for Lactuca sativa quality of digestate biofertilizer from the co-digestion of food waste and human
and Daucus carota crops. J. Plant Nutr. Soil Sci. 176, 876–882. excreta. Waste Manag. 34, 747–752.
Frampton, R.A., Pitman, A.R., Fineran, P.C., 2012. Advances in bacteriophage-mediated Oyeleye, A., Normi, Y., 2018. Chitinase: diversity, limitations, and trends in engineering
control of plant pathogens. Int.J.Microbiol. 2012, 326452. for suitable applications. Biosci. Rep. 38, BSR20180323.
Garénaux, A., Caza, M., Dozois, C.M., 2011. The Ins and Outs of siderophore mediated Pandey, P.K., Vaddella, V., Cao, W., Biswas, S., Chiu, C., Hunter, S., 2016. In-vessel
iron uptake by extra-intestinal pathogenic Escherichia coli. Vet. Microbiol. 153, composting system for converting food and green wastes into pathogen free soil
89–98. amendment for sustainable agriculture. J. Clean. Prod. 139, 407–415.
Glick, B.R., 2005. Modulation of plant ethylene levels by the bacterial enzyme ACC Panuccio, M.R., Attinà, E., Basile, C., Mallamaci, C., Muscolo, A., 2016. Use of
deaminase. FEMS Microbiol. Lett. 251, 1–7. recalcitrant agriculture wastes to produce biogas and feasible biofertilizer.
Glick, B.R., 2014. Bacteria with ACC deaminase can promote plant growth and help to WasteBiomass Valorization 7, 267–280.
feed the world. Microbiol. Res. 169, 30–39. Park, K.-H., Lee, C.-Y., Son, H.-J., 2009. Mechanism of insoluble phosphate solubilization
Gruber, S., Seidl-Seiboth, V., 2012. Self versus non-self: fungal cell wall degradation in by Pseudomonas fluorescens RAF15 isolated from ginseng rhizosphere and its plant
trichoderma. Microbiology 158, 26–34. growth-promoting activities. Lett. Appl. Microbiol. 49, 222–228.
Gunjal, B.B., 2019. In: Value-added Products From Food Waste, pp. 20–30. Phua Choo Kwai, H., Khairuddin Abdul, R., Ahmad Nazrul Abd, W., 2009. Evaluation of
Hakim, A., Jaganath, S., Honnabyraiah, M., Kumar, S., Dayamani, K.S.A., 2018. gamma irradiation and heat treatment by autoclaving in the preparation of
Influence of biofertilizer and auxin on growth and rooting of pomegranate (Punica microorganism-free carriers for biofertilizer products. Jurnal Sains Nuklear Malays.
granatum L.) cuttings. Int. J. Curr. Microbiol. Appl. Sci. 7. 21, 1–5.
Hamid, Q., Ali, M.H., Tseng, M.-L., Lan, S., Kumar, M., 2020. Impeding challenges on Puglia, D., Pezzolla, D., Gigliotti, G., Torre, L., Bartucca, M.L., Del Buono, D., 2021. The
industry 4.0 in circular economy: palm oil industry in Malaysia. Comput. Oper. Res. opportunity of valorizing agricultural waste, through its conversion into
123, 105052. biostimulants, biofertilizers, and biopolymers. Sustainability 13, 2710.
Ibiene, A., Agogbua, J., Okonko, I., Nwachi, G.N., 2012. Plant growth promoting Radzki, W., Mañero, F., Algar, E., Lucas, J., García-Villaraco, A., Ramos, B., 2013.
rhizobacteria (PGPR) as bio-fertilizer: effect on growth of Lycopersicum esculentus. Bacterial siderophores efficiently provide iron to iron-starved tomato plants in
J. Am. Sci. 8, 318–324. hydroponics culture. Antonie van Leeuwenhoek 104.
Jakobsen, I., Leggett, M.E., Richardson, A.E., 2005. In: Rhizosphere Microorganisms And Ravikumar, S., Kathiresan, K., Ignatiammal, S.T.M., Babu Selvam, M., Shanthy, S., 2004.
Plant Phosphorus Uptake, Phosphorus: Agriculture And the Environment, Nitrogen-fixing azotobacters from mangrove habitat and their utility as marine
pp. 437–494. biofertilizers. J. Exp. Mar. Biol. Ecol. 312, 5–17.
Karthikeyan, B., Joe, M., Islam, M.R., Sa, T., 2012. ACC deaminase containing Reddy, S., Singh, A., Masih, H., Benjamin, J., Ojha, S., Ramteke, P., Singla, A., 2018. In:
diazotrophic endophytic bacteria ameliorate salt stress in Catharanthus roseus Effect of Azotobacter sp. and Azospirillum sp. on vegetative growth of tomato
through reduced ethylene levels and induction of antioxidative defense systems. (Lycopersicon esculentum), 7, pp. 2130–2137.
Symbiosis 56, 77–86. Rigby, H., Smith, S.R., 2013. Nitrogen availability and indirect measurements of
Leaungvutiviroj, C., Ruangphisarn, P., Hansanimitkul, P., Shinkawa, H., Sasaki, K., 2010. greenhouse gas emissions from aerobic and anaerobic biowaste digestates applied to
Development of a new biofertilizer with a high capacity for N2 fixation, phosphate agricultural soils. Waste Manag. 33, 2641–2652.
and potassium solubilization and auxin production. Biosci. Biotechnol. Biochem. 74, Ritika, B., Utpal, D., 2014. Biofertilizer, a way towards organic agriculture: a review. Afr.
1098–1101. J. Microbiol. Res. 8, 2332–2343.
Leghari, S.J., Wahocho, N.A., Laghari, G.M., HafeezLaghari, A., MustafaBhabhan, G., Rossi, C., Pereira, M., García, A., Luis, R., Berbara, L., Gazolla, P., Perin, A., Paz-
HussainTalpur, K., Bhutto, T.A., Wahocho, S.A., Lashari, A.A., 2016. Role of nitrogen González, A., 2016. Effects on the composition and structural properties of the
for plant growth and development: a review. Adv. Environ. Biol. 10, 209+. humified organic matter of soil in sugarcane strawburning: a chronosequence study
Lehman, S., Sholberg, P., Roach, D., Castle, A., 2011. In: Phage Biopesticides And Soil in the Brazilian Cerrado of Goiás State. Agric. Ecosyst. Environ. 216, 34.
Bacteria: Multilayered And Complex Interactions, pp. 215–235. Saleem, M., Arshad, M., Hussain, S., Bhatti, A., 2007. Perspective of plant growth
Lu, Q., Zhao, Y., Gao, X., Wu, J., Zhou, H., Tang, P., Wei, Q., Wei, Z., 2018. Effect of promoting rhizobacteria (PGPR) containing ACC deaminase in stress agriculture.
tricarboxylic acid cycle regulator on carbon retention and organic component J. Ind. Microbiol. Biotechnol. 34, 635–648.
transformation during food waste composting. Bioresour. Technol. 256. Satlewal, A., Agrawal, R., Bhagia, S., Das, P., Ragauskas, A.J., 2018. Rice straw as a
Ma, Y., Yin, Y., Liu, Y., 2017. New insights into co-digestion of activated sludge and food feedstock for biofuels: availability, recalcitrance, and chemical properties. Biofuels
waste: biogas versus biofertilizer. Bioresour. Technol. 241. Bioprod. Biorefin. 12, 83–107.
Madhaiyan, M., Poonguzhali, S., Sa, T., 2007. Characterization of 1-aminocyclopropane- Senoo, K., Kaneko, M., Taguchi, R., Murata, J., Santasup, C., Tanaka, A., Obata, H., 2002.
1-carboxylate (ACC) deaminase containing Methylobacterium oryzae and Enhanced growth and nodule occupancy of red kidney bean and soybean inoculated
interactions with auxins and ACC regulation of ethylene in canola (Brassica with soil aggregate-based inoculant. Soil Sci.Plant Nutr. 48, 251–259.
campestris). Planta 226, 867–876. Shamsuddin, M.R., May, A., Hau, L., Aqsha, A., Mansor, N., Narasimha, M., 2020.
Mahami, T., Togby-Tetteh, W., Kottoh, D.I., Amoakoah-Twum, L., Gasu, E., Annan, S.N. Investigation of pesticidal ability of humic acid derived from palm oil Empty Fruit
Y., Larbi, D., Adjei, I., Adu-Gyamfi, A., 2019. Microbial food safety risk to humans Bunch (EFB) vermicompost. <sb:contribution><sb:title>Int. J. Recycl. Org.
associated with poultry feed: the role of irradiation. Int. J. Food Sci. 2019, 6915736. Waste</sb:title></sb:contribution><sb:host><sb:issue><sb:series><sb:
Mahmud, M.S., Chong, K.P., 2021. Formulation of biofertilizers from oil palm empty fruit title>Agric.</sb:title></sb:series></sb:issue></sb:host> 9.
bunches and plant growth-promoting microbes: a comprehensive and novel Singh, R.P., Shelke, G.M., Kumar, A., Jha, P.N., 2015. Biochemistry and genetics of ACC
approach towards plant health. J.King Saud Univ.Sci. 33, 101647. deaminase: a weapon to "stress ethylene" produced in plants. Front. Microbiol. 6,
937-937.

7
M.Y. Areeshi International Journal of Food Microbiology 374 (2022) 109719

Singh, M., Singh, D., Gupta, A., Pandey, K.D., Singh, P.K., Kumar, A., 2019. Chapter three Truckell, I.G., Shah, S.H., Baillie, I.C., Hallett, S.H., Sakrabani, R., 2019. Soil and
- plant growth promoting rhizobacteria: application in biofertilizers and biocontrol transport factors in potential distribution systems for biofertilisers derived from
of phytopathogens. In: Singh, A.K., Kumar, A., Singh, P.K. (Eds.), PGPR Amelioration palm oil mill residues in Malaysia. Comput. Electron. Agric. 166, 105005.
in Sustainable Agriculture. Woodhead Publishing, pp. 41–66. Tsai, S.-H., Liu, C.-P., Yang, S.-S., 2007. Microbial conversion of food wastes for
Soumare, A., Boubekri, K., Lyamlouli, K., Hafidi, M., Ouhdouch, Y., Kouisni, L., 2020. biofertilizer production with thermophilic lipolytic microbes. Renew. Energy 32,
From isolation of phosphate solubilizing microbes to their formulation and use as 904–915.
biofertilizers: status and needs. Front. Bioeng. Biotechnol. 7. Uçkun Kiran, E., Trzcinski, A.P., Ng, W.J., Liu, Y., 2014. Bioconversion of food waste to
Stan, D., Enciu, A.-M., Mateescu, A.L., Ion, A.C., Brezeanu, A.C., Stan, D., Tanase, C., energy: a review. Fuel 134, 389–399.
2021. Natural compounds with antimicrobial and antiviral effect and nanocarriers Vejan, P., Abdullah, R., Khadiran, T., Ismail, S., Nasrulhaq Boyce, A., 2016. Role of plant
used for their transportation. Front. Pharmacol. 12. growth promoting rhizobacteria in agricultural sustainability—a review. Molecules
Svircev, A.M., Lehman, S.M., Sholberg, P., Roach, D., Castle, A.J., 2011. Phage 21, 573.
biopesticides and soil bacteria: multilayered and complex interactions. In: Vurukonda, S.S.K.P., Giovanardi, D., Stefani, E., 2018. Plant growth promoting and
Witzany, G. (Ed.), Biocommunication in Soil Microorganisms. SpringerBerlin biocontrol activity of Streptomyces spp. as endophytes. Int. J. Mol. Sci. 19, 952.
Heidelberg, Berlin, Heidelberg, pp. 215–235. Walia, A., Guleria, S., Chauhan, A., Mehta, P., 2017. Endophytic bacteria: role in
Tampio, E., Marttinen, S., Rintala, J., 2016. Liquid fertilizer products from anaerobic phosphate solubilization. In: Maheshwari, D.K., Annapurna, K. (Eds.), Endophytes:
digestion of food waste: mass, nutrient and energy balance of four digestate liquid Crop Productivity And Protection, Volume 2. Springer International Publishing,
treatment systems. J. Clean. Prod. 125, 22–32. Cham, pp. 61–93.
Tilak, K.V.B.R., Ranganayaki, N., Manoharachari, C., 2006. Synergistic effects of plant- Zhang, H., Liu, Y., Wang, G., 2019. Integrated use of maize bran residue for one-step
growth promoting rhizobacteria and Rhizobium on nodulation and nitrogen fixation phosphate bio-fertilizer production. Appl. Biochem. Biotechnol. 187, 1475–1487.
by pigeonpea (Cajanus cajan). Eur. J. Soil Sci. 57, 67–71. Zhao, Y., 2010. Auxin biosynthesis and its role in plant development. Annu. Rev. Plant
Biol. 61, 49–64.

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