Enhanced performance of the microalga Chlorella sorokiniana remotely induced by the plant growth-promoting bacteria Azospirillum brasilense and Bacillus pumilus

A Revised Medium for Rapid Growth and Bio Assays with Tobacco Tissue Cultures

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A RAPID METHOD OF TOTAL LIPID EXTRACTION AND PURIFICATION

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Colorimetric Method for Determination of Sugars and Related Substances

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A RAPID METHOD OF TOTAL LIPID EXTRACTION AND PURIFICATION

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Bacterial volatiles promote growth in Arabidopsis

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Advances in plant growth-promoting bacterial inoculant technology: formulations and practical perspectives (1998–2013)

Yoav Bashan, A., de‐Bashan, L. E., Prabhu, S. R., & Hernández, J.-P. (2013) · Plant and Soil · doi:10.1007/s11104-013-1956-x · Cited by 1,475 · see citing works

Bacterial Volatiles Induce Systemic Resistance in Arabidopsis

Ryu, C.-M., Farag, M. A., Hu, C.-H., Reddy, M. S., Kloepper, J. W., & Paré, P. W. (2004) · PLANT PHYSIOLOGY · doi:10.1104/pp.103.026583 · Cited by 1,308 · see citing works

Indole as an intercellular signal in microbial communities

Lee, J.-H., & Lee, J. (2010) · FEMS Microbiology Reviews · doi:10.1111/j.1574-6976.2009.00204.x · Cited by 1,059 · see citing works

Bacterial volatiles: the smell of small organisms

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Promotion of Plant Growth by Bacterial ACC Deaminase

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Immobilized microalgae for removing pollutants: Review of practical aspects

de‐Bashan, L. E., & Yoav Bashan, A. (2009) · Bioresource Technology · doi:10.1016/j.biortech.2009.09.043 · Cited by 788 · see citing works

Bacterial volatiles and their action potential

Kai, M., Haustein, M., Molina, F., Petri, A., Scholz, B. K., & Piechulla, B. (2008) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-008-1760-3 · Cited by 562 · see citing works

Volatile Mediated Interactions Between Bacteria and Fungi in the Soil

Effmert, U., Kalderás, J., Warnke, R., & Piechulla, B. (2012) · Journal of Chemical Ecology · doi:10.1007/s10886-012-0135-5 · Cited by 526 · see citing works

Rhizobacterial volatile emissions regulate auxin homeostasis and cell expansion in Arabidopsis

Zhang, H., Kim, M.-S., Krishnamachari, V., Payton, P., Sun, Y., Grimson, M., Farag, M. A., Ryu, C.-M., Allen, R., Melo, I. S., et al. (2007) · Planta · doi:10.1007/s00425-007-0530-2 · Cited by 515 · see citing works

mVOC: a database of microbial volatiles

Lemfack, M. C., Nickel, J., Dunkel, M., et al. (2013) · Nucleic Acids Research · doi:10.1093/nar/gkt1250 · Cited by 480 · see citing works

Production of plant growth modulating volatiles is widespread among rhizosphere bacteria and strongly depends on culture conditions

Blom, D., Fabbri, C., Connor, E. C., Schiestl, F. P., Klauser, D., Böller, T., Eberl, L., & Weisskopf, L. (2011) · Environmental Microbiology · doi:10.1111/j.1462-2920.2011.02582.x · Cited by 380 · see citing works

Efficiency of ammonia and phosphorus removal from a colombian agroindustrial wastewater by the microalgae Chlorella vulgaris and Scenedesmus dimorphus

Gonzalez, L. E., Cañizares, R., & Baena, S. (1997) · Bioresource Technology · doi:10.1016/s0960-8524(97)00029-1 · Cited by 369 · see citing works

GC–MS SPME profiling of rhizobacterial volatiles reveals prospective inducers of growth promotion and induced systemic resistance in plants

Farag, M. A., Ryu, C., Sumner, L. W., & Paré, P. W. (2006) · Phytochemistry · doi:10.1016/j.phytochem.2006.07.021 · Cited by 360 · see citing works

Increased Growth of the Microalga <i>Chlorella vulgaris</i> when Coimmobilized and Cocultured in Alginate Beads with the Plant-Growth-Promoting Bacterium <i>Azospirillum brasilense</i>

Gonzalez, L. E., & Bashan, Y. (2000) · Applied and Environmental Microbiology · doi:10.1128/aem.66.4.1527-1531.2000 · Cited by 304 · see citing works

Dynamic Chemical Communication between Plants and Bacteria through Airborne Signals: Induced Resistance by Bacterial Volatiles

Farag, M. A., Zhang, H., & Ryu, C. (2013) · Journal of Chemical Ecology · doi:10.1007/s10886-013-0317-9 · Cited by 287 · see citing works

Diffusible signals and interspecies communication in bacteria

Ryan, R. P., & Dow, J. M. (2008) · Microbiology · doi:10.1099/mic.0.2008/017871-0 · Cited by 284 · see citing works

Identification of bacteria and bacteria-associated chemical cues that mediate oviposition site preferences by <i>Aedes aegypti</i>

Ponnusamy, L., Xu, N., Nojima, S., Wesson, D. M., Schal, C., & Apperson, C. S. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0802505105 · Cited by 244 · see citing works

Microalgal Heterotrophic and Mixotrophic Culturing for Bio-refining: From Metabolic Routes to Techno-economics

Perez‐Garcia, O., & Yoav Bashan, A. (2015) · Springer eBooks · doi:10.1007/978-3-319-20200-6_3 · Cited by 239 · see citing works

GacS-Dependent Production of 2R, 3R-Butanediol by Pseudomonas chlororaphis O6 Is a Major Determinant for Eliciting Systemic Resistance Against Erwinia carotovora but not Against Pseudomonas syringae pv. tabaci in Tobacco

Han, S. H., Lee, S. J., Moon, J. H., Park, K. H., Yang, K. Y., Cho, B. H., Kim, K. Y., Kim, Y. W., Lee, M. C., Anderson, A. J., et al. (2006) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi-19-0924 · Cited by 238 · see citing works

Azospirillum Genomes Reveal Transition of Bacteria from Aquatic to Terrestrial Environments

Wisniewski‐Dyé, F., Borziak, K., Khalsa-Moyers, G., Alexandre, G. M., Sukharnikov, L. O., Wuichet, K., Hurst, G. B., McDonald, W. H., Robertson, J. S., Barbe, V., et al. (2011) · PLoS Genetics · doi:10.1371/journal.pgen.1002430 · Cited by 238 · see citing works

The modulating effect of bacterial volatiles on plant growth

Bailly, A., & Weisskopf, L. (2012) · Plant Signaling & Behavior · doi:10.4161/psb.7.1.18418 · Cited by 234 · see citing works

Alginate beads provide a beneficial physical barrier against native microorganisms in wastewater treated with immobilized bacteria and microalgae

Covarrubias, S. A., de‐Bashan, L. E., Moreno, M., & Yoav Bashan, A. (2011) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-011-3585-8 · Cited by 232 · see citing works

Increased pigment and lipid content, lipid variety, and cell and population size of the microalgae <i>Chlorella</i> spp. when co-immobilized in alginate beads with the microalgae-growth-promoting bacterium <i>Azospirillum brasilense</i>

de-Bashan, L. E., Bashan, Y., Moreno, M., Lebsky, V. K., & Bustillos, J. J. (2002) · Canadian Journal of Microbiology · doi:10.1139/w02-051 · Cited by 222 · see citing works

INVOLVEMENT OF INDOLE‐3‐ACETIC ACID PRODUCED BY THE GROWTH‐PROMOTING BACTERIUM AZOSPIRILLUM SPP. IN PROMOTING GROWTH OF CHLORELLA VULGARIS1

de‐Bashan, L. E., Antoun, H., & Bashan, Y. (2008) · Journal of Phycology · doi:10.1111/j.1529-8817.2008.00533.x · Cited by 214 · see citing works

Volatile Organic Compounds and Microorganisms

Stotzky, G., Schenck, S., & Papavizas, G. C. (1976) · CRC Critical Reviews in Microbiology · doi:10.3109/10408417609102303 · Cited by 200 · see citing works

Microdetermination of lipids and serum total fatty acids

Pande, S. V., Khan, R. P., & Venkitasubramanian, T. A. (1963) · Analytical Biochemistry · doi:10.1016/0003-2697(63)90094-0 · Cited by 185 · see citing works

Growth promotion of the freshwater microalga Chlorella vulgaris by the nitrogen-fixing, plant growth-promoting bacterium Bacillus pumilus from arid zone soils

Hernández, J.-P., de‐Bashan, L. E., Rodríguez, D., Rodríguez, Y., & Yoav Bashan, A. (2008) · European Journal of Soil Biology · doi:10.1016/j.ejsobi.2008.08.004 · Cited by 181 · see citing works

Acetate metabolism by Escherichia coli in high-cell-density fermentation

Kleman, G. L., & Strohl, W. R. (1994) · Applied and Environmental Microbiology · doi:10.1128/aem.60.11.3952-3958.1994 · Cited by 175 · see citing works

Volatile organic compounds from rhizobacteria increase biosynthesis of essential oils and growth parameters in peppermint (Mentha piperita)

Santoro, M. V., Zygadlo, J. A., Giordano, W. F., & Banchio, E. (2011) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2011.07.016 · Cited by 175 · see citing works

Two different modes of attachment of Azospirillum brasilense Sp7 to wheat roots

Michiels, C. W., Croes, C., & Vanderleyden, J. (1991) · Journal of General Microbiology · doi:10.1099/00221287-137-9-2241 · Cited by 174 · see citing works

Phenethyl Alcohol and Tryptophol: Autoantibiotics Produced by the Fungus Candida albicans

Lingappa, B. T., Prasad, M., Lingappa, Y., et al. (1969) · Science · doi:10.1126/science.163.3863.192 · Cited by 172 · see citing works

Effects of CO2 concentrations on the freshwater microalgae, Chlamydomonas reinhardtii, Chlorella pyrenoidosa and Scenedesmus obliquus (Chlorophyta)

Yang, Y., & Gao, K. (2003) · Journal of Applied Phycology · doi:10.1023/a:1026021021774 · Cited by 171 · see citing works

Assessment of affinity and specificity of Azospirillum for plants

Pereg, L. L., de‐Bashan, L. E., & Yoav Bashan, A. (2015) · Plant and Soil · doi:10.1007/s11104-015-2778-9 · Cited by 156 · see citing works

A volatile organic compound analysis from Arthrobacter agilis identifies dimethylhexadecylamine, an amino-containing lipid modulating bacterial growth and Medicago sativa morphogenesis in vitro

Velázquez-Becerra, C., Macías‐Rodríguez, L., López‐Bucio, J., Altamirano-Hernández, J., Flores-Cortéz, I., & Valencia‐Cantero, E. (2010) · Plant and Soil · doi:10.1007/s11104-010-0583-z · Cited by 141 · see citing works

Enhanced accumulation of starch and total carbohydrates in alginate-immobilized Chlorella spp. induced by Azospirillum brasilense: II. Heterotrophic conditions

Choix, F. J., de-Bashan, L. E., & Bashan, Y. (2012) · Enzyme and Microbial Technology · doi:10.1016/j.enzmictec.2012.07.012 · Cited by 133 · see citing works

Plant growth promotion due to rhizobacterial volatiles – An effect of CO2?

Kai, M., & Piechulla, B. (2009) · FEBS Letters · doi:10.1016/j.febslet.2009.09.053 · Cited by 132 · see citing works

Alpha terpineol: a potential anticancer agent which acts through suppressing NF-kappaB signalling.

Hassan, S. B., Gali‐Muhtasib, H. U., Göransson, H., & Larsson, R. L. (2010) · PubMed · Cited by 130 · see citing works

Bacillus pumilus ES4: Candidate plant growth-promoting bacterium to enhance establishment of plants in mine tailings

de‐Bashan, L. E., Hernández, J.-P., Bashan, Y., et al. (2010) · Environmental and Experimental Botany · doi:10.1016/j.envexpbot.2010.04.014 · Cited by 99 · see citing works

Environmental Stress Physiology

Vonshak, A., & Torzillo, G. (2003) · doi:10.1002/9780470995280.ch4 · Cited by 98 · see citing works

Chemical Defense in the Stink Bug Cosmopepla bimaculata

Krall, B. S., Bartelt, R. J., Lewis, C. J., et al. (1999) · Journal of Chemical Ecology · doi:10.1023/a:1020822107806 · Cited by 93 · see citing works

Cultivation factors and population size control the uptake of nitrogen by the microalgae Chlorella vulgaris when interacting with the microalgae growth-promoting bacterium Azospirillum brasilense

de‐Bashan, L. E., Hani Antoun, A., & Yoav Bashan, A. (2005) · FEMS Microbiology Ecology · doi:10.1016/j.femsec.2005.03.014 · Cited by 92 · see citing works

Effects of Escherichia coli on Mixotrophic Growth of Chlorella minutissima and Production of Biofuel Precursors

Higgins, B. T., & VanderGheynst, J. S. (2014) · PLoS ONE · doi:10.1371/journal.pone.0096807 · Cited by 89 · see citing works

Root surface colonization of non-cereal crop plants by pleomorphic Azospirillum brasilense Cd

Bashan, Y., Levanony, H., & Whitmoyer, R. E. (1991) · Microbiology · doi:10.1099/00221287-137-1-187 · Cited by 89 · see citing works

Volatiles and primary metabolites profiling in two Hibiscus sabdariffa (roselle) cultivars via headspace SPME - GC-MS and chemometrics

Farag, M. A., Rasheed, D. M., & Kamal, I. M. (2015) · Food Research International · doi:10.1016/j.foodres.2015.09.024 · Cited by 88 · see citing works

Joint Immobilization of Plant Growth-Promoting Bacteria and Green Microalgae in Alginate Beads as an Experimental Model for Studying Plant-Bacterium Interactions

de‐Bashan, L. E., & Yoav Bashan, A. (2008) · Applied and Environmental Microbiology · doi:10.1128/aem.00518-08 · Cited by 85 · see citing works

Establishment of stable synthetic mutualism without co-evolution between microalgae and bacteria demonstrated by mutual transfer of metabolites (NanoSIMS isotopic imaging) and persistent physical association (Fluorescent in situ hybridization)

de-Bashan, L. E., Mayali, X., Bebout, B. M., Weber, P. K., Detweiler, A. M., Hernandez, J. P., Prufert-Bebout, L., & Bashan, Y. (2016) · Algal Research · doi:10.1016/j.algal.2016.02.019 · Cited by 79 · see citing works

Ultrastructural localization and identification ofAzospirillum brasilense Cd on and within wheat root by immuno-gold labeling

Levanony, H., Bashan, Y., Romano, B., et al. (1989) · Plant and Soil · doi:10.1007/bf02220714 · Cited by 77 · see citing works

Microbial Volatile Emissions Promote Accumulation of Exceptionally High Levels of Starch in Leaves in Mono- and Dicotyledonous Plants

Ezquer, I., Li, J., Ovečka, M., Baroja‐Fernández, E., Muñoz, F. J., Montero, M., de Cerio, J. D., Hidalgo, M., Sesma, M. T., Bahaji, A., et al. (2010) · Plant and Cell Physiology · doi:10.1093/pcp/pcq126 · Cited by 77 · see citing works

Root-surface colonization of black mangrove seedlings by Azospirillum halopraeferens and Azospirillum brasilense in seawater

Puente, M. E., Holguín, G., Glick, B. R., et al. (1999) · FEMS Microbiology Ecology · doi:10.1111/j.1574-6941.1999.tb00619.x · Cited by 75 · see citing works

Horizontal and Vertical Movement of Azospirillum brasilense Cd in the Soil and along the Rhizosphere of Wheat and Weeds in Controlled and Field Environments

Bashan, Y., & Levanony, H. (1987) · Microbiology · doi:10.1099/00221287-133-12-3473 · Cited by 74 · see citing works

Enhanced accumulation of starch and total carbohydrates in alginate-immobilized Chlorella spp. induced by Azospirillum brasilense: I. Autotrophic conditions

Choix, F. J., de-Bashan, L. E., & Bashan, Y. (2012) · Enzyme and Microbial Technology · doi:10.1016/j.enzmictec.2012.07.013 · Cited by 72 · see citing works

Volatiles Profiling in Medicinal Licorice Roots Using Steam Distillation and Solid‐Phase Microextraction (SPME) Coupled to Chemometrics

Farag, M. A., & Wessjohann, L. A. (2012) · Journal of Food Science · doi:10.1111/j.1750-3841.2012.02927.x · Cited by 70 · see citing works

Development of two culture media for mass cultivation of Azospirillum spp. and for production of inoculants to enhance plant growth

Bashan, Y., Trejo, A., & de‐Bashan, L. E. (2011) · Biology and Fertility of Soils · doi:10.1007/s00374-011-0555-3 · Cited by 69 · see citing works

CELL‐CELL INTERACTION IN THE EUKARYOTE‐PROKARYOTE MODEL OF THE MICROALGAE CHLORELLA VULGARIS AND THE BACTERIUM AZOSPIRILLUM BRASILENSE IMMOBILIZED IN POLYMER BEADS1

de‐Bashan, L. E., Schmid, M., Rothballer, M., Hartmann, A., & Yoav Bashan, A. (2011) · Journal of Phycology · doi:10.1111/j.1529-8817.2011.01062.x · Cited by 64 · see citing works

Mechanism of Algal Aggregation by Bacillus sp. Strain RP1137

Powell, R. J., & Hill, R. T. (2014) · Applied and Environmental Microbiology · doi:10.1128/aem.00887-14 · Cited by 63 · see citing works

Evidence for a Weak Active External Adsorption of Azospirillum brasilense Cd to Wheat Roots

Bashan, Y., Levanony, H., & Klein, E. (1986) · Microbiology · doi:10.1099/00221287-132-11-3069 · Cited by 62 · see citing works

Involvement of indole-3-acetic acid produced by Azospirillum brasilense in accumulating intracellular ammonium in Chlorella vulgaris

Meza, B., de-Bashan, L. E., & Bashan, Y. (2015) · Research in Microbiology · doi:10.1016/j.resmic.2014.12.010 · Cited by 61 · see citing works

Comparison of differently coated SPME fibres applied for monitoring volatile substances in vegetable oils

Doleschall, F., Recseg, K., Kemény, Z., et al. (2003) · European Journal of Lipid Science and Technology · doi:10.1002/ejlt.200390070 · Cited by 60 · see citing works

Accumulation fatty acids of in Chlorella vulgaris under heterotrophic conditions in relation to activity of acetyl-CoA carboxylase, temperature, and co-immobilization with Azospirillum brasilense

Leyva, L. A., Yoav Bashan, A., Mendoza, A., & de‐Bashan, L. E. (2014) · Die Naturwissenschaften · doi:10.1007/s00114-014-1223-x · Cited by 57 · see citing works

Enhanced activity of ADP glucose pyrophosphorylase and formation of starch induced by Azospirillum brasilense in Chlorella vulgaris

Choix, F. J., Bashan, Y., Mendoza, A., & de-Bashan, L. E. (2014) · Journal of Biotechnology · doi:10.1016/j.jbiotec.2014.02.014 · Cited by 56 · see citing works

Interactions between Acetoin, a Plant Volatile, and Pheromone In Rhynchophorus palmarum: Behavioral and Olfactory Neuron Responses

Saïd, I., Renou, M., Morin, J., et al. (2005) · Journal of Chemical Ecology · doi:10.1007/s10886-005-5927-4 · Cited by 50 · see citing works

Impact of volatiles of the rhizobacteriaSerratia odoriferaon the mossPhyscomitrella patens

Kai, M., & Piechulla, B. (2010) · Plant Signaling & Behavior · doi:10.4161/psb.5.4.11340 · Cited by 49 · see citing works

Comparative Mass Spectrometry & Nuclear Magnetic Resonance Metabolomic Approaches for Nutraceuticals Quality Control Analysis: A Brief Review

Farag, M. A. (2014) · Recent Patents on Biotechnology · doi:10.2174/1389201014666131218125035 · Cited by 45 · see citing works

Effects of low temperatures (9–33 °C) and pH (3.3–5.7) in the loss of Saccharomyces cerevisiae viability by combining lethal concentrations of ethanol with octanoic and decanoic acids

Viegas, C. A. (1997) · International Journal of Food Microbiology · doi:10.1016/s0168-1605(96)01200-7 · Cited by 35 · see citing works

Chlorella sorokiniana (formerly C. vulgaris) UTEX 2714, a non-thermotolerant microalga useful for biotechnological applications and as a reference strain

Yoav Bashan, A., López, B. R., Huss, V. A. R., Amavizca, E., & de‐Bashan, L. E. (2015) · Journal of Applied Phycology · doi:10.1007/s10811-015-0571-z · Cited by 31 · see citing works

Adsorption and anchoring of Azospirillumstrains to roots of wheat seedlings

Pinheiro, R. D., Boddey, L. H., James, E. K., et al. (2002) · Plant and Soil · doi:10.1023/a:1020645203084 · Cited by 30 · see citing works

Growth Promotion of Tobacco Plant by 3-hydroxy-2-Butanone from Bacillus vallismortis EXTN-1

Ann, M., Cho, Y. E., Ryu, H. J., Kim, H. T., & Park, K. (2013) · The Korean Journal of Pesticide Science · doi:10.7585/kjps.2013.17.4.388 · Cited by 26 · see citing works

Ammonia causes necrosis in tomato leaves infected with Pseudomonas tomato (Okabe) Alstatt

Bashan, Y., Okon, Y., & Henis, Y. (1980) · Physiological Plant Pathology · doi:10.1016/0048-4059(80)90012-0 · Cited by 26 · see citing works

Unexpected Phytostimulatory Behavior for Escherichia coli and Agrobacterium tumefaciens Model Strains

Walker, V., Bruto, M., Bellvert, F., et al. (2013) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi-12-12-0298-r · Cited by 25 · see citing works

Molecular features of a defined genetic marker for the determination of the Porphyra tenera lineage

Kunimoto, M., Kito, H., Mizukami, Y., et al. (2003) · Journal of Applied Phycology · doi:10.1023/a:1025182508440 · Cited by 22 · see citing works

Interaction of Azospirillum spp. with Microalgae: A Basic Eukaryotic–Prokaryotic Model and Its Biotechnological Applications

de‐Bashan, L. E., Hernández, J.-P., & Yoav Bashan, A. (2015) · Springer eBooks · doi:10.1007/978-3-319-06542-7_20 · Cited by 18 · see citing works

On the natural occurrence of (−)-3-carene, a component of termite defense secretions

Valterová, I., Vrkoč, J., Lindström, M., et al. (1992) · Die Naturwissenschaften · doi:10.1007/bf01138574 · Cited by 10 · see citing works

The interactions of algae-activated sludge symbiotic system and its effects on wastewater treatment and lipid accumulation

Chen, X., Hu, Z., Qi, Y., Song, C., & Chen, G. (2019) · Bioresource Technology · doi:10.1016/j.biortech.2019.122017 · Cited by 161 · see citing works

Toward the Enhancement of Microalgal Metabolite Production through Microalgae–Bacteria Consortia

González-González, L. M., & de-Bashan, L. E. (2021) · Biology · doi:10.3390/biology10040282 · Cited by 133 · see citing works

Co-culture of Chlorella and wastewater-borne bacteria in vinegar production wastewater: enhancement of nutrients removal and influence of algal biomass generation

Huo, S., Kong, M., Zhu, F., Qian, J., Huang, D., Chen, P., & Ruan, R. (2020) · Algal Research · doi:10.1016/j.algal.2019.101744 · Cited by 114 · see citing works

Enhancing algal biomass and lipid production through bacterial co-culture

Berthold, D. E., Shetty, K. G., Jayachandran, K., Laughinghouse, H. D., & Gantar, M. (2019) · Biomass and Bioenergy · doi:10.1016/j.biombioe.2019.01.033 · Cited by 86 · see citing works

Tryptophan, thiamine and indole-3-acetic acid exchange between Chlorella sorokiniana and the plant growth-promoting bacterium Azospirillum brasilense

Palacios, O. A., Gómez-Anduro, G. A., Yoav Bashan, A., & de‐Bashan, L. E. (2016) · FEMS Microbiology Ecology · doi:10.1093/femsec/fiw077 · Cited by 90 · see citing works

Influence of tryptophan and indole-3-acetic acid on starch accumulation in the synthetic mutualistic Chlorella sorokiniana–Azospirillum brasilense system under heterotrophic conditions

Palacios, O. A., Choix, F. J., Yoav Bashan, A., & de‐Bashan, L. E. (2016) · Research in Microbiology · doi:10.1016/j.resmic.2016.02.005 · Cited by 38 · see citing works

Effect of plant growth promoting rhizobacteria on bacterial canker of tomato

Girish, N., & Umesha, S. (2005) · Archives of Phytopathology and Plant Protection · doi:10.1080/03235400500094704 · Cited by 49 · see citing works

COMPARATIVE ANALYSIS OF DISINTEGRATION METHODS OF CHLORELLA SOROKINIANA CELLS THAT INCREASE THE EFFICIENCY OF EXTRACTION OF INTRACELLULAR WATER-SOLUBLE PROTEINS

Temnov, M. S., Ustinskaya, Y. V., Eskova, M., et al. (2022) · IZVESTIYA VYSSHIKH UCHEBNYKH ZAVEDENIY KHIMIYA KHIMICHESKAYA TEKHNOLOGIYA · doi:10.6060/ivkkt.20226504.6527 · Cited by 3 · see citing works

Azospirillum brasilense reduces oxidative stress in the green microalgae Chlorella sorokiniana under different stressors

Peng, H., de‐Bashan, L. E., & Higgins, B. T. (2020) · Journal of Biotechnology · doi:10.1016/j.jbiotec.2020.10.029 · Cited by 40 · see citing works