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Plant growth-promoting endophytic bacteria on maize and sorghum1

Bactérias endofíticas promotoras de crescimento em milho e sorgo

ABSTRACT

Plant growth-promoting bacteria (PGPB) are found in plant tissues and promote plant growth by secretion of hormones and enzymes, or by facilitating the nutrient uptake. This study assessed forty PGPB isolates to determine their effects on maize and sorghum growth. These isolates were also compared with uninoculated plants, as negative (-N; without N fertilization) and positive (+N; with N fertilization) controls. Plant height, stem diameter, shoot and root dry mass, leaf N accumulation and chlorophyll content were evaluated. For both the maize and sorghum, the height, stem diameter and shoot dry mass in plants inoculated with PGPB were similar to those of uninoculated plants supplied with N, and the responses for root mass were higher than in plants supplied with N. However, the PGPB isolates did not promote N accumulation and chlorophyll content similar to those of uninoculated plants supplied with N. The IPACC26 and IPACC30 isolates, both identified as Bacillus subtilis, resulted in better responses for plant growth and N accumulation than the other isolates.

KEYWORDS:
Bacillus subtilis; nitrogen accumulation; chlorophyll

RESUMO

Bactérias promotoras de crescimento em plantas (BPCP) são encontradas em tecidos vegetais e promovem o crescimento vegetal por meio da secreção de hormônios e enzimas, ou auxiliando a absorção de nutrientes. Avaliaram-se quarenta isolados de BPCP para determinar seus efeitos sobre o crescimento de milho e sorgo. Estes isolados foram também comparados com plantas não inoculadas, como controles negativos (-N; sem fertilização nitrogenada) e positivos (+N; com fertilização nitrogenada). A altura, diâmetro de caule, massas secas da parte aérea e raízes, acúmulo de N e conteúdo de clorofila foram avaliados. Em ambos o milho e o sorgo, a altura, diâmetro do caule e a massa seca da parte aérea em plantas inoculadas com BPCP foram similares aos das plantas não inoculadas e fertilizadas com N, e as respostas da massa das raízes foram maiores que das plantas fertilizadas com N. Entretanto, os isolados de BPCP não promoveram acúmulo de N e conteúdo de clorofila semelhantes aos das plantas não inoculadas e fertilizadas com N. IPACC26 e IPACC30, ambos identificados como Bacillus subtilis, apresentaram melhores respostas para o crescimento das plantas e acúmulo de N do que os outros isolados.

PALAVRAS-CHAVE:
Bacillus subtilis; acúmulo de nitrogênio; clorofila

INTRODUCTION

Plant growth-promoting bacteria (PGPB) are microorganisms that can improve the plant performance in many different ways (Palacios et al. 2014PALACIOS, A. O.; BASHAN, Y.; DE-BASHAN, L. E. Proven and potential involvement of vitamins in interactions of plants with plant growth-promoting bacteria: an overview. Biology and Fertility of Soils, v. 50, n. 3, p. 415-432, 2014.). These bacteria directly or indirectly promote the plant growth by secretion of hormones and enzymes, or by facilitating the uptake and accumulation of nutrients such as nitrogen (N) and phosphorus (P) (Ahemad & Kibret 2014AHEMAD, M.; KIBRET, M. Mechanisms and applications of plant growth promoting rhizobacteria: current perspective. Journal of King Saud University-Science, v. 26, n. 1, p. 1-20, 2014.). They can also protect plants from pathogens, improve the soil structure and degrade pollutants (Hayat et al. 2010HAYAT, R. Soil beneficial bacteria and their role in plant growth promotion: a review. Annals of Microbiology, v. 60, n. 4, p. 579-598, 2010.).

Several bacteria genera are classified as PGPB, including Bacillus,Pseudomonas,Rhizobium,Bradyrhizobium and Azospirillum.Bacillus and Pseudomonas influence the plant growth mainly by the synthesis of plant hormones (e.g., auxin, cytokinin and gibberellins) and production of siderophores and antibiotics (Adesemoye et al. 2008ADESEMOYE, A. O.; OBINI, M.; UGOJI, E. O. Comparison of plant growth-promotion with Pseudomonas aeruginosa and Bacillus subtilis in three vegetables. Brazilian Journal of Microbiology, v. 39, n. 3, p. 423-426, 2008.). On the other hand, Rhizobium and Bradyrhizobium are involved in the biological N fixation in leguminous plants (Sulieman & Tran 2014SULIEMAN, S.; TRAN, L. S. Symbiotic nitrogen fixation in legume nodules: metabolism and regulatory mechanisms. International Journal of Molecular Sciences, v. 15, n. 11, p. 19389-19393, 2014.), while Azospirillum acts on non-leguminous plants (Santi et al. 2013SANTI, C.; BOGUSZ, D.; FRANCHE, C. Biological nitrogen fixation in non-legume plants. Annals of Botany, v. 111, n. 5, p. 743-767, 2013.) and can also synthetize phytohormones such as indole-3-acetic acid (Fukami et al. 2018FUKAMI, J.; CEREZINI, P.; HUNGRIA, M. Azospirillum: benefits that go far beyond biological nitrogen fixation. AMB Express, v. 8, n. 1, p. 73, 2018.). The inoculation with rhizobacteria can enhance the plant development and productivity. Studies have shown that Bacillus and Pseudomonas increase the soybean and wheat growth (Araujo 2008ARAUJO, F. F. Inoculação de sementes com Bacillus subtilis, formulado com farinha de ostras e desenvolvimento de milho, soja e algodão. Ciência e Agrotecnologia, v. 32, n. 2, p. 456-462, 2008., Sharma et al. 2011SHARMA, S. K.; JOHRI, B. N.; RAMESH, A.; JOSHI, O. P.; SAI PRASAD, S. V. Selection of plant growth-promoting Pseudomonas spp. that enhanced productivity of soybean-wheat cropping system in central India. Journal of Microbiology & Biotechnology, v. 21, n. 11, p. 1127-1142, 2011.). Similarly, Azospirillum,Rhizobium and Bradyrhizobium promote the growth of sugarcane (Schultz et al. 2014SCHULTZ, N.; SILVA, J. A.; SOUSA, J. S.; MONTEIRO, R. C.; OLIVEIRA, R. P.; CHAVES, V. A.; PEREIRA, W.; SILVA, M. F.; BALDANI, J. I.; BODDEY, R. M.; REIS, V. M.; URQUIAGA, S. Inoculation of sugarcane with diazotrophic bacteria. Revista Brasileira de Ciência do Solo, v. 38, n. 2, p. 407-414, 2014.), common bean (Chekanai et al. 2018CHEKANAI, V.; CHIKOWO, R.; VANLAUWE, B. Response of common bean (Phaseolus vulgaris L.) to nitrogen, phosphorus and rhizobia inoculation across variable soils in Zimbabwe. Agriculture, Ecosystems & Environment, v. 266, n. 1, p. 167-173, 2018.) and soybean (Ulzen et al. 2016ULZEN, J.; ULZEN, J.; ABAIDOO, R. C.; MENSAH, N. E.; MASSO, C.; ABDELGADIR, A. H. Bradyrhizobium inoculants enhance grain yields of soybean and cowpea in northern Ghana. Frontiers in Plant Science, v. 7, n. 7, p. 1770-1780, 2016.).

Maize and sorghum are two important cereal crops in Brazil, with a production of about 102 million tons, in 2019 (IBGE 2019Instituto Brasileiro de Geografia e Estatística (IBGE). Levantamento sistemático da produção agrícola. Rio de Janeiro: IBGE, 2019.). Usually, maize and sorghum producers plant these crops in soils with nutrient deficits and, therefore, PGPB could contribute to the enhancement of plant biomass and nutrient uptake. Studies in Brazil have shown positive effects of PGPB on plant growth and yield in maize (Araujo & Guerreiro 2010ARAÚJO, F. F.; GUERREIRO, R. T. Bioprospecção de isolados de Bacillus promotores de crescimento de milho cultivado em solo autoclavado e natural. Ciência e Agrotecnologia, v. 34, n. 4, p. 837-844, 2010.) and sorghum (Schlemper et al. 2018SCHLEMPER, T. R.; DIMITROV, M. R.; SILVA GUTIERREZ, F. A. O.; VAN VEEN, J. A.; SILVEIRA, A. P. D.; KURAMAE, E. E. Effect of Burkholderia tropica and Herbaspirillum frisingense strains on sorghum growth is plant genotype dependent. Peer J, v. 6, e5346, 2018.). However, it is important to select suitable bacteria isolates and evaluate their growth-promoting abilities.

In this study, several PGPB that were isolated from sugarcane and presented high biochemical and plant growth-promotion abilities (Antunes 2016ANTUNES, J. E. L. Bactérias diazotróficas endofíticas em cana-de-açúcar: estratégia para uma agricultura sustentável. 2016. Tese (Doutorado em Ciência do Solo) - Universidade Federal Rural de Pernambuco, Recife, 2016.) were evaluated for their ability to promote growth in maize and sorghum. As sugarcane belongs to the gramineae group as maize and sorghum, the hypothesis is that PGPB isolated from sugarcane would promote the maize and sorghum growth.

MATERIAL AND METHODS

The study was conducted at the Universidade Federal do Piauí, in Teresina, Piauí state, Brazil, from March to June 2018. A total of 40 PGPB isolates (Table 1), obtained in leaves and stalks of sugarcane by Antunes et al. (2017)ANTUNES, J. E. L.; LYRA, M. C. C. P.; OLLERO, F. J.; FREITAS, A. D. S.; OLIVEIRA, L. M. S.; ARAÚJO, A. S. F.; FIGUEIREDO, M. V. B. Diversity of plant growth-promoting bacteria associated with sugarcane. Genetics and Molecular Research, v. 16, n. 2, gmr16029662, 2017., were inoculated into seeds of sorghum (Sorghum bicolor cv. Palo Alto N52K1009) and maize (Zea mays cv. AG-1051). Therefore, two separate experiments (sorghum and maize), in a completely randomized design, with three replicates, were conducted in a growth chamber, to assess the reaction of both crops to the isolates (treatments). These isolates were also compared with uninoculated negative (-N; without N fertilization) and positive (+N; with N fertilization) controls.

Table 1
Plant growth-promoting bacteria (PGPB) isolates used in this study as inoculants for maize and sorghum.

To prepare the inoculants, the PGPB isolates were individually grown in Erlenmeyer flasks containing 50 mL of liquid culture medium (Tryptic Soy Broth - TSB at 25 %) and incubated under orbital shaking (200 rpm and 31 ºC) for 72 h. The bacterial growth was verified by measuring the optical density using a spectrophotometer (wavelength of 540 nm), and a final concentration of 109 CFU mL-1 was considered for inoculation.

The experimental units consisted of pots (0.8 dm3) containing 0.7 dm3 of sterile sand (pH 6.8) that were autoclaved (120 ºC at 101 kPa) for 60 min. The autoclaving procedure was repeated three times. Sorghum and maize seeds were surface disinfected with alcohol (70 %) for 30 s, followed by sodium hypochlorite (2 %) for 60 s, and then washed with sterile distilled water. Seeds were directly inoculated with 1 mL aliquots of the cell suspensions containing the PGPB isolates. Plants were grown under a photoperiod cycle of 14 h of light at 28 ºC and 10 h of darkness at 20 ºC. Every 3 days, 2 mL of the Hoagland’s nutrient solution (Hoagland & Arnon 1950HOAGLAND, D. R.; ARNON, D. I. The water-culture method for growing plants without soil. Berkeley: California Agricultural Experiment Station, 1950.), without N, were added to each pot. The positive control (+N) received 50 mg pot-1 and 75 mg pot-1 of N for sorghum and maize, respectively, in accordance with their individual N requirements. These rates were applied, after diluting with water, five times during the experiment (10 mL pot-1). Sorghum and maize were maintained for 30 and 45 days, respectively, before being harvested. The plant height and stem diameter were measured. Shoots and roots were dried at 65 ºC to a constant mass, to determine their dry mass. The N content in leaves was evaluated using the Kjeldahl method (Bremner & Mulvaney 1982BREMNER, J. M.; MULVANEY, C. S. Nitrogen-total. In: PAGE, A. L.; MILLER, R. H.; KEENEY, D. R. (ed.). Methods of soil analysis: Part 2. Chemical and microbiological properties. Madison: American Society of Agronomy, 1982. p. 595-624.) and the chlorophyll content was estimated using spectrophotometric methods (Lichtenthaler & Wellburn 1983LICHTENTHALER, H.; WELLBURN, A. Determinations of total carotenoids and chlorophylls a and b of leaf extracts in different solvents. Biochemical Society Transactions, v. 11, n. 6 , p. 591-592, 1983.).

Analyses of variance and F-tests at 5 % of significance were performed to estimate and test the effects of the isolates on both crops (maize and sorghum). Data normality was verified by the Shapiro-Wilk test, and treatment means were compared by using the Scott-Knott test, also at 5 % of significance.

RESULTS AND DISCUSSION

The PGPB treatment showed significant effects on all the evaluated variables in maize and sorghum (Table 2). The PGPB isolates had similar or higher growth effects on maize and sorghum, if compared to the growth of uninoculated plants supplied with N.

Table 2
Analyses of variance and F-test values for treatment effects on growth variables1 1 Height: plant height; diameter: stem diameter; SDW: shoot dry weight; RDW: root dry weight; Nitrogen: N accumulation; Chlorophyll: chlorophyll content. in maize and sorghum trials, with plants inoculated or not with plant growth-promoting bacteria.

Thus, the majority of the isolates promoted an increased height in maize and sorghum similar to that of plants supplied with N (Figure 1). Notably, 17 PGPB isolates promoted a higher stem diameter in maize than in uninoculated maize plants supplied with N (Figure 2).

Figure 1
Plant height of maize (a) and sorghum (b) inoculated with plant growth-promoting bacteria isolates. Means followed by the same letter do not differ significantly at 5 % by the Scott-Knott test. -N: uninoculated plants without N fertilization; +N: uninoculated plants with N fertilization.

Figure 2
Stem diameter of maize (a) and sorghum (b) inoculated with plant growth-promoting bacteria isolates. Means followed by the same letter do not differ significantly at 5 % by the Scott-Knott test. -N: uninoculated plants without N fertilization; +N: uninoculated plants with N fertilization.

Few isolates were able to promote an increase in the shoot dry mass in maize (Figure 3A), while the majority of the isolates promoted similar increases in the sorghum shoot dry mass, if compared to that in uninoculated plants supplied with N (Figure 3B). Interestingly, the majority of the isolates promoted an increased root growth (Figure 4A), while few isolates promoted an increase in the sorghum root growth (Figure 4B) higher than that of plants supplied with N. Notably, the inoculation of the isolates IPACC24 (B. subtilis) in maize and IPACC59 (unidentified) in sorghum yielded the highest ability to promote the root growth.

Figure 3
Shoot dry weight (SDW) of maize (a) and sorghum (b) inoculated with plant growth-promoting bacteria isolates. Means followed by the same letter do not differ significantly at 5 % by the Scott-Knott test. -N: uninoculated plants without N fertilization; +N: uninoculated plants with N fertilization.

Figure 4
Root dry weight (RDW) of maize (a) and sorghum (b) inoculated with plant growth-promoting bacteria isolates. Means followed by the same letter do not differ significantly at 5 % by the Scott-Knott test. -N: uninoculated plants without N fertilization; +N: uninoculated plants with N fertilization.

These results indicate that the evaluated PGPB promoted a similar or even an increased growth of maize and sorghum, when compared to plants that received only N fertilization. Since a low N availability is usually the main factor that limits the growth and yield of crops (Bhattacharjee et al. 2008BHATTACHARJEE, R.; SINGH, A.; MUKHOPADHYAY, S. N. Use of nitrogen-fixing bacteria as biofertiliser for non-legumes: prospects and challenges. Applied Microbiology Biotechnology, v. 80, n. 2, p. 199-209, 2008.), these results are important for tropical regions where these PGPB could present a potential alternative to decrease the use of N fertilizers. The promotion of plant growth by PGPB is already known and it involves, among others, biochemical capabilities, production of phytohormones such as indole-3-acetic acid (IAA) and the process of biological nitrogen fixation (Souza et al. 2015SOUZA, R. D.; AMBROSINI, A.; PASSAGLIA, L. M. Plant growth-promoting bacteria as inoculants in agricultural soils. Genetics and Molecular Biology, v. 38, n. 4, p. 401-419, 2015.). Indeed, these PGPB isolates presented a high capability of producing IAA and performing the biological N fixation in sugarcane (Antunes et al. 2017ANTUNES, J. E. L.; LYRA, M. C. C. P.; OLLERO, F. J.; FREITAS, A. D. S.; OLIVEIRA, L. M. S.; ARAÚJO, A. S. F.; FIGUEIREDO, M. V. B. Diversity of plant growth-promoting bacteria associated with sugarcane. Genetics and Molecular Research, v. 16, n. 2, gmr16029662, 2017.), and could also promote the maize and sorghum growth. Previous studies have shown positive growth responses in maize and sorghum, when inoculated with PGPB (Schlemper et al. 2018SCHLEMPER, T. R.; DIMITROV, M. R.; SILVA GUTIERREZ, F. A. O.; VAN VEEN, J. A.; SILVEIRA, A. P. D.; KURAMAE, E. E. Effect of Burkholderia tropica and Herbaspirillum frisingense strains on sorghum growth is plant genotype dependent. Peer J, v. 6, e5346, 2018., Widawati & Suliasih 2018WIDAWATI, S.; SULIASIH, M. The effect of plant growth promoting rhizobacteria (PGPR) on germination and seedling growth of Sorghum bicolor L. Moench. Earth and Environmental Science, v. 166, e012022, 2018.). Similarly, Arruda et al. (2013)ARRUDA, L.; BENEDUZI, A.; MARTINS, A.; LISBOA, B.; LOPES, C.; BERTOLO, F.; PASSAGLIA, L. M. P.; VARGAS, L. K. Screening of rhizobacteria isolated from maize (Zea mays L.) in Rio Grande do Sul state (south Brazil) and analysis of their potential to improve plant growth. Applied Soil Ecology, v. 63, n. 1, p. 15-22, 2013. observed that the inoculation of maize with different bacteria significantly promoted root (50-68 %) and shoot (25-54 %) growth.

Interestingly, root growth was the parameter that presented positive and significant responses to the isolates, even when comparing with the responses of uninoculated plants supplied with N. Thus, some isolates enhanced the root growth in maize and sorghum. The increased root growth may be attributed to the synthesis of plant growth-regulating substances, such as IAA, produced by these isolates (Antunes et al. 2017ANTUNES, J. E. L.; LYRA, M. C. C. P.; OLLERO, F. J.; FREITAS, A. D. S.; OLIVEIRA, L. M. S.; ARAÚJO, A. S. F.; FIGUEIREDO, M. V. B. Diversity of plant growth-promoting bacteria associated with sugarcane. Genetics and Molecular Research, v. 16, n. 2, gmr16029662, 2017.), which coordinates the developmental processes in plants and promotes a higher root development by increasing the lateral and adventitious root formation (Duca et al. 2014DUCA, D.; LORV, J.; PATTEN, C. L.; ROSE, D.; GLICK, B. R. Indole-3-acetic acid in plant-microbe interactions. Antonie Van Leeuwenhoek, v. 106, n. 1, p. 85-125, 2014.). This significant increase in root growth promoted by some PGPB may be important for maize and sorghum growth, since roots anchor plants and absorb and conduct nutrients and water (Maloof 2004MALOOF, J. N. Plant development: slowing root growth naturally. Current Biology, v. 14, n. 10, p. R395-R396, 2004.). Youseif (2018)YOUSEIF, S. H. Genetic diversity of plant growth promoting rhizobacteria and their effects on the growth of maize plants under greenhouse conditions. Annals of Agricultural Sciences, v. 63, n. 1, p. 25-35, 2018. observed a significant increase in root growth in maize with inoculation of 49 PGPB isolates and attributed it to the high ability of synthetizing IAA. According to Vikram et al. (2007)VIKRAM, A.; KRISHNARAJ, P. U.; HAMZEHZARGHANI, H.; JAGADEESH, K. S. Growth promotional potential of Pseudomonas fluorescens FPD 10 and its interaction with Bradyrhizobium sp. Research Journal of Microbiology, v. 2, n. 4, p. 354-361, 2007., the IAA produced by the bacteria may positively influence the development of the root system, improving the nutrient absorption required for plant growth.

Neither the PGPB isolates nor the uninoculated plants supplied with N promoted a N accumulation and chlorophyll content. However, the majority of isolates promoted a N accumulation in maize (Figure 5A) and sorghum (Figure 5B), if compared to uninoculated plants without N.

Figure 5
Nitrogen accumulated in maize (a) and sorghum (b) shoot inoculated with plant growth-promoting bacteria isolates. Means followed by the same letter do not differ significantly at 5 % by the Scott-Knott test. -N: uninoculated plants without N fertilization; +N: uninoculated plants with N fertilization.

The isolates IPACC23 (Paenibacillus sp.), IPACC26 (B. subtilis), IPACC30 (B. subtilis), IPACC33 (Pseudomonas sp.), IPACF44 (Burkholderia sp.), IPACF47a (Paenibacillus sp.) and IPACF48 (Brevibacillus agri) presented the most efficient N accumulation in maize, while IPACC26 (B. subtilis) and IPACC30 (B. subtilis) were more efficient in sorghum. Similarly, the majority of the isolates promoted an increased chlorophyll content in maize (Figure 6A) and sorghum (Figure 6B). For both crops, IPACC26 (B.subtilis) and IPACF66 (Pseudomonas sp.) presented the highest increase in the chlorophyll content.

Figure 6
Chlorophyll content in maize (a) and sorghum (b) shoot inoculated with plant growth-promoting bacteria isolates. Means followed by the same letter do not differ significantly at 5 % by the Scott-Knott test. -N: uninoculated plants without N fertilization; +N: uninoculated plants with N fertilization.

These results show that both the maize and sorghum could benefit from the increased N accumulation and chlorophyll content promoted by the inoculation with PGPB. However, the isolates could not increase the N accumulation and chlorophyll content as in plants supplied with N. On the other hand, since the inoculated plants did not receive additional N, the accumulation of N resulted from biological N fixation. Although these isolates did not present similar capabilities to increase the N accumulation and chlorophyll content as it happened after the N fertilization, they show a potential as N supplements to plants.

According to Kuan et al. (2016)KUAN, K. B.; OTHMAN, R.; ABDUL RAHIM, K.; SHAMSUDDIN, Z. H. Plant growth-promoting rhizobacteria inoculation to enhance vegetative growth, nitrogen fixation and nitrogen remobilization of maize under greenhouse conditions. PLoS One, v. 11, n. 3, e0152478, 2016., PGPB may provide a biological alternative to fix N from the atmosphere. These endophytic bacteria colonize plant tissues, such as roots, stem and leaves, and can fix N for use by plants (James et al. 1997JAMES, E. K.; OLIVARES, F. L.; BALDANI, J. I.; DÖBEREINER, J. Herbaspirillum an endophytic diazotroph colonizing vascular tissue in leaves of Sorghum bicolor L. Moench. Journal of Experimental Botany, v. 48, n. 3, p. 785-798, 1997.). The inoculation with PGPB in maize and sorghum leads to a significantly increased N accumulation (Alagawadi & Gaur 1992ALAGAWADI, A. R.; GAUR, A. C. Inoculation of Azospirillum brasilense and phosphate-solubilizing bacteria on yield of sorghum [Sorghum bicolor (L.) Moench] in dry land. Tropical Agriculture, v. 69, n. 4, p. 347-350, 1992., Kuan et al. 2016KUAN, K. B.; OTHMAN, R.; ABDUL RAHIM, K.; SHAMSUDDIN, Z. H. Plant growth-promoting rhizobacteria inoculation to enhance vegetative growth, nitrogen fixation and nitrogen remobilization of maize under greenhouse conditions. PLoS One, v. 11, n. 3, e0152478, 2016.). In this study, several PGPB isolates contributed to an increased chlorophyll content in maize and sorghum, suggesting an indirect effect, since the chlorophyll content is directly correlated with the N accumulation in plants (Liu et al. 2012LIU, Z. A.; YANG, J. P.; YANG, Z. C. Using a chlorophyll meter to estimate tea leaf chlorophyll and nitrogen contents. Journal of Soil Science and Plant Nutrition, v. 12, n. 2, p. 339-348, 2012.). Previous studies have shown a significant effect of PGPB on the chlorophyll content in maize (Almaghrabi et al. 2014ALMAGHRABI, O. A.; ABDELMONEIM, T. S.; ALBISHRI, H. M.; MOUSSA, T. A. A. Enhancement of maize growth using some plant growth promoting rhizobacteria (PGPR) under laboratory conditions. Life Science Journal, v. 11, n. 11, p. 764-772, 2014.) and wheat (Turan et al. 2012TURAN, M.; GULLUCE, M.; ŞAHIN, F. Effects of plant-growth-promoting rhizobacteria on yield, growth, and some physiological characteristics of wheat and barley plants. Communications in Soil Science and Plant Analysis, v. 43, n. 12, p. 1658-1673, 2012.). Consistently with the results of previous studies, B. subtilis was the most efficient in promoting the N accumulation and, consequently, increased the chlorophyll content in maize (Lima et al. 2015LIMA, F. F., NUNES, L. A. P. L.; FIGUEIREDO, M. V. B.; ARAUJO, F. F.; LIMA, L. M.; ARAUJO, A. S. F. Bacillus subtilis e adubação nitrogenada na produtividade do milho. Revista Brasileira de Ciências Agrárias, v. 6, n. 4, p. 657-661, 2015., Pupathy & Radziah 2015PUPATHY, U. T.; RADZIAH, O. Growth response of corn to nitrogen-fixing bacteria enriched compost. Asian Journal of Crop Science, v. 7, n. 1, p. 72-80, 2015.) and sorghum (Das et al. 2010DAS, I. K.; ANNAPURNA, A.; SEETHARAMA, N. Rhizosphere competence of biocontrol agent Bacillus subtilis strain SRB28 from sorghum. Indian Phytopathology, v. 63, n. 4, p. 375-379, 2010.). The isolates that promoted the highest N accumulation in maize and sorghum also presented a high ability to fix N in sugarcane (Antunes et al. 2017ANTUNES, J. E. L.; LYRA, M. C. C. P.; OLLERO, F. J.; FREITAS, A. D. S.; OLIVEIRA, L. M. S.; ARAÚJO, A. S. F.; FIGUEIREDO, M. V. B. Diversity of plant growth-promoting bacteria associated with sugarcane. Genetics and Molecular Research, v. 16, n. 2, gmr16029662, 2017.). This confirms that Bacillus can fix N from the atmosphere (Mollica et al. 1985MOLLICA, M. L.; VAN ELSAS, J. D.; PENIDO, E. G. C. An improved method to detect acetylene-reducing activity in Bacillus strains. Journal of Microbiological Methods, v. 3, n. 3-4, p. 147-157, 1985.). Studies have shown that Pseudomonas species can also fix molecular N and, thus, stimulate the accumulation of N and chlorophyll in maize (Kifle & Laing 2016KIFLE, M. H.; LAING, M. D. Isolation and screening of bacteria for their diazotrophic potential and their influence on growth promotion of maize seedlings in greenhouses. Frontiers in Plant Science, v. 6, e1225, 2016.) and sorghum (Praveen et al. 2012PRAVEEN, K. G.; DESAI, S.; AMALRAJ, E. L. D.; AHMED, S. K. M. H.; REDDY, G. Plant growth promoting Pseudomonas spp. from diverse agro-ecosystems of India for Sorghum bicolor L. Journal of Biofertilizers and Biopesticides, v. 7, n. 1, p. 1-8 , 2012.). Finally, our results show that these isolates present a potential for promoting maize and sorghum growth and, consequently, yield. Therefore, the inoculation with these isolates may be an ecological alternative for decreasing the dependence on N fertilizers.

CONCLUSIONS

  1. Plant growth-promoting bacteria (PGPB) isolates may potentially be used as biological inoculants to increase the N accumulation and growth of maize and sorghum;

  2. Most of the tested PGBP isolates promote growth in maize and sorghum;

  3. The IPACC26 and IPACC30 isolates, both identified as Bacillus subtilis, have a better effect on the N accumulation in maize and sorghum.

REFERENCES

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Publication Dates

  • Publication in this collection
    25 Nov 2019
  • Date of issue
    2019

History

  • Received
    11 Dec 2018
  • Accepted
    21 May 2019
  • Published
    16 Oct 2019
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