Chemical Analysis, Antioxidant, and Antibacterial Potential of Aqueous Extract of Broccoli (Brassica oleracea) Using GC-ms

Document Type : Original Articles

Authors

1 Chemistry Department, College of Science, University of Babylon, Babylon, Iraq

2 Department of Medical Laboratory Techniques, Al-Mustaqbal University College, 51001 Hillah, Babylon, Iraq

3 Nanotechnology and Advanced Materials Research Centre, University of Technology, Baghdad, Iraq

4 Medical Physics Department, Hilla University College, Babylon, Iraq

5 Department of Chemical Engineering, College of Engineering, University of Babylon, Babylon, Iraq

6 Babil Teaching Hospital For Maternity and Children, Babylon, Iraq

Abstract

Antioxidant and antibacterial chemicals are key sources in medicinal plants. Alkaloids, phenolics, steroids, terpenes, flavonoids, terpenes, and volatile oils are a few of these plants' secondary metabolites. Phytochemicals, particularly the secondary metabolites produced by plants, are important for human nutrition, well-being, illness prevention, and antibacterial properties. This study aimed to ascertain the aqueous broccoli extract's chemical makeup. The phytochemical molecule that the GC-MS technique identified. The DPPH assay, which is appropriate for regular plant material screening, was performed to assess the antioxidant capacities of broccoli extract (in vitro). Subsequently looks at how well they perform against different Gram-positive and Gram-negative harmful microorganisms. GC-MS analysis of Broccoli extract revealed the existence of the9-Octadecenamide, [C18H35O], Hexadecane [c16h34] and 2, 2, 2-trifluoroethyl 2-methyltetrahydro-5-oxo-3- furancarboxylate [C23H33NO6]. There were significant changes in the extract's ascorbic acid-free radical scavenging activity at 200, 100, and 25 g/ml (P 0.05), and the activity was dose-dependent. The effectiveness of aqueous broccoli extract as a powerful, broad-spectrum antibacterial agent against tested bacteria is demonstrated by an increase in the diameter of the inhibition zone, which increases in direct proportion to the concentration of the extract and even surpasses the activity of some antibiotics. An appropriate concentration of aqueous broccoli extract strongly inhibits microbial and antioxidant growth, especially when treating external infections without any danger against resistant bacterial isolates; it is strongly advised to use aqueous broccoli extract as a cost-effective alternative antibacterial and antioxidant agent.

Keywords

Main Subjects


1. Introduction

Broccoli (Brassica oleracea) is an edible green vegetable, a fast-growing annual plant that belongs to the family Brassicaceae. The pharmaceutical importance of broccoli has been enormously reported as an anticancer, immunomodulator, antidiabetic, antimicrobial, hepatoprotective, cardioprotective, antiamnesic, and antioxidant. Cruciferous vegetables have high fiber content, low calories, and are rich in vitamins and minerals, which are beneficial for normal human physiological functions. Though there are various reports on the benefits of broccoli as a crude vegetable, our focus was to analyze the phytochemical constituents, antioxidant and antibacterial activities, and investigate bioactive compounds obtained by extraction ( 1 - 7 ).

The best method for locating the bioactive components of substances like long-chain hydrocarbons, acids, esters, steroids, alkaloids, alcohols, amino compounds, and nitro compounds is GC-MS. Gas chromatography (GC) and Mass spectroscopy (MS), along with specific detection tests, have therefore developed into sophisticated methods for analyzing a variety of compounds ( 8 ). Brassica oleracea, sometimes broccoli, is an Italian vegetable member of the Brassicaceae family ( 9 ). The plant is frequently used to cure various illnesses, including bleeding, diarrhea, poisoning, and eye disorders. It also acts as an anti-inflammatory, analgesic, and antioxidant. Our research is focused on identifying possible sources of medicinal plants using cutting-edge scientific techniques analysis like Gas Chromatography-Mass Spectrometry, that advances in biotechnology science have evaluated natural compounds quickly, faster, and more precisely than before techniques, resulting in the isolation of effective compounds with body health benefits. As a fundamental technical platform for secondary metabolite profiling in plant and non-plant species during the past few years, gas chromatography-mass spectrometry (GC-MS) has solidified its position ( 9 , 10 ).

A number of regulatory mechanisms, including cell growth, death, and gene expression, are regulated by free radicals produced during aerobic metabolism. Free radicals may damage vital cell biomolecules by oxidizing membrane lipids, cell proteins, carbohydrates, DNA, and enzymes when they are produced in excess. This can undermine the antioxidant system's capacity to protect the body from free radical damage. Malonyl dialdehyde and 4-hydroxynonenal are two examples of harmful substances that are produced as a result of oxidative stress. It also affects the oxidant-antioxidant balance (redox equilibrium), which is essential for healthy cell function ( 11 - 13 ).

Parkinson's disease, Alzheimer's, alcohol-induced liver disease, atherosclerosis, mild cognitive impairment, ulcerative colitis, and aging are all pathologies brought on by oxidative stress ( 14 - 23 ). Antioxidants can break chains by quenching singlet oxygen, dissolving hydroperoxides, chelating prooxidative metal ions, and scavenging chain-starting radicals like hydroxyl, alkoxyl, or peroxyl ( 24 ). According to epidemiological research, consuming fruits and vegetables high in antioxidant-rich components can reduce the occurrence of illnesses linked to oxidative stress. Antioxidant-rich foods and minerals significantly impact prevention ( 25 - 28 ).

Resistance to antibiotics is a great threat in the present therapeutic era ( 29 ). Researchers worldwide are working tirelessly to find a new drug moiety with antimicrobial potential to overcome the resistance factor. Unfortunately, the new antimicrobial drug molecules under trial also do not guarantee they will overcome the resistance-related issues. Therefore, the scientific focus for the past decade has shifted to green vegetables, which are more beneficial, like day-to-day food habits ( 30 - 32 ).

In Iraq, no studies have been conducted on broccoli's chemical components, antioxidants, or antibacterial effects. The current experiment aimed to assess the amounts of various components, antioxidant activity, and antibacterial activity from aqueous broccoli extract.

2. Materials and Methods

2.1. Gas Chromatography-Mass Spectrometry Analysis

Shimadzu's (QP-2010) gas chromatograph mass spectrometer in Tokyo, Japan, an AOC-20i auto-sampler, and a DB-5MS capillary column, measuring 30 m x 0.25 mm i. d., 0.25 m, were used to analyze the chemical hydrolytic products. The sample injection volume was 2 l in GC grade DCM, and the column's temperature was set to 230°C for 15 minutes after being programmed to 230°C at a rate of 4°C/min. At a flow rate of 1.1 ml/min in split mode, helium was employed as the carrier gas (1:50) ( 33 ).

2.2. DPPH Radical Assay

According to the method given by 50 to the ascertained activity of aqueous broccoli extract, the DPPH (1, 1-diphenyl, 2-picryl-hydrazine) free radical scavenging was performed. Different amounts of broccoli extract (12.5, 25, 50, and 100 g/ml) are utilized. Spectrophotometric calculations were made using the ELISA reader to determine how well samples scavenged the stable DPPH radical. When the DPPH decrease was evaluated at 517 nm, the colorimetric transition (from deep violet to bright yellow) (Figure 1). A good example of a positive control is ascorbic acid (as a reference). The equation below has been used to compute the inhibition percentage (34):

Antioxidant activity %=ODcontrol-ODsampleODcontrol×100

Figure 1. Radical scavenging of DPPH• to DPPH-H by Aqueous Broccoli extract

2.3. Bacterial Isolates, Solution, Media

The teaching hospital in Hillah, Iraq, provided the bacterial isolates collected from its patients. All samples underwent normal bacteriological procedures, including isolation and purification by growing on agar plates ofMacConkey's and blood agar for 24-48 hours at 37°C. By using the Biomérieux Vitek-2 compact system, all isolates were verified.

Mueller-Hinton media and Mueller-Hinton agar were obtained from Hi-Media (Mumbai, India). Different antibiotic disks ceftriaxone (CRO-3Oµg), ampicillin (AM-10µg), cephalothin (KF-30µg), chloramphenicol (C-30µg), and meropenem (MEM-10µg) were purchased from (Bioanalyse, Turkey( ( 34 ).

2.4. Antibacterial Activity of Broccoli Extract

Two G+ve bacteria (Streptococcus mutants and Staphylococcus epidermidis) and two Gve bacteria (Pseudomonas aeruginosa and Escherichia coli) were storage on nutrient agar slants when the antibacterial activity of aqueous broccoli extract was evaluated against various human pathogenic bacteria. The Clinical and Laboratory Standards Institute's guidelines for antibacterial activity were followed ( 35 ). A disk diffusion experiment is performed to examine the efficacy of broccoli extract against the study bacteria as well as the antibiotic sensitivity of the bacteria. Concentrations of aqueous broccoli extract (500, 250, 125, and 62.5 g/ml) in sterile deionized water are employed in triplicates. The isolates underwent a 15-minute at-room-temperature incubation followed by overnight incubation at 37 °C. After a specified incubation time, we visible the inhibition with a clear zone surrounding the well. Positive findings were noted when the inhibition zone's width was always measured using a digital Vernier caliper ( 36 ).

3. Results and Discussion

The National Institute of Standards and Technology database was used to interpret the GC-MS (NIST) mass spectrum. The spectrum of the known component contained in the NIST library was compared to the mass spectrum of the unknown component. The main elements were determined using absolute standards and by recording from electronic libraries. The test materials' peak area, molecular weight, chemical name, probability, molecular formula, biological activity, and peak area were determined. The relative percentage quantity of each component was computed by comparing each component's average peak area to the sum of all areas.

Figure 2 displays the GC-MS analysis findings for the aqueous broccoli extract. The constituents 9-Octadecenamide, (Z) [C18H35O] (35.217), Hexadecane [c16h34] (36.899) and 2, 2, 2-trifluoroethyl 2-methyltetrahydro-5-oxo-3- furancarboxylate [C23H33NO6](37.681) .

Figure 2. GC-MS analysis of aqueous Broccoli extract

Figure 2 illustrates distinct components with varied retention durations based on the GC-MS spectra. To determine the kind and structure of the chemicals, the mass spectrometer examines the substances eluted at various periods. A peak with a different m/z ratio appears as the significant component breaks up into more minor compounds. These mass spectra serve as the data library's fingerprint for the molecule, making them valuable. Numerous phytochemicals that significantly contribute to the pharmacological activity of broccoli were found in the aqueous extract of the plant, according to GC-MS analysis.

3.1. DPPH Assay

The antioxidant activity of aqueous broccoli extract was determined using the DPPH test, which used ascorbic acid as a control. The extract had equivalent free radical scavenging activity to the control in the current investigation. The antioxidant activity of aqueous broccoli extract in concentrations of (200, 100, 50, and 25) μg/ml was significantly highest (75.2 percent at 200 μg/ml), while extract in concentrations of (100, 50, and 25 μg/ml) showed antioxidant activity (68.01, 53.52, and 36.04 percent) respectively, and ascorbic acid's antioxidant properties at the same concentration was (80.00, 70.40, 56.60, and 40.09 μg/ml (Figure 3).

Figure 3. DPPH of water Aqueous Broccoli extract

In the doses of 200, 100, and 25 μg/ml, where there were significant differences (P≤0.05) compared to control, aqueous broccoli extract production showed a similar free radical scavenging pattern action as ascorbic acid. These findings demonstrated that the extract's DPPH free radical scavenging activity was dosage-dependent. Additionally, suspension stability can be achieved by adsorbing the quinoid chemical produced when the phenol group in phenolics is oxidized on the surface of nanoparticles ( 37 , 38 ). It is generally known that phenolic chemicals may have a direct role in antioxidant activity ( 39 ). Because of their redox properties, which enable them to function as reducing agents, hydrogen donors, and singlet oxygen quenchers, plant phenolics are hypothesized to have an antioxidant effect ( 40 ).

Aqueous Broccoli extract can help with vascular changes, particularly endothelial dysfunction caused by oxidative stress ( 35 ). This syndrome can cause a decrease in NO(nitric oxide) bioavailability, impacting vascular tone control and endothelial dysfunction—the initial stage of cardiovascular disease development. As a result, a plant extract with antioxidant characteristics developed in this work might be used to treat vascular dysfunction caused by hypertension, diabetes, or atherosclerosis.

3.2. Antibacterial Activity of Broccoli Extract

Aqueous broccoli extract demonstrates broad-spectrum solid antibacterial activity when tested against microorganisms resistant to many drugs. Different antibiotics' effects on all bacterial isolates under study were compared. According to the findings in figures 47, not all chosen antibiotics are effectively against the chosen bacterial strains. Aqueous broccoli extract demonstrated an increase in inhibitory zone width with their concentration, even surpassing the action of several antibiotics Pseudomonas aeruginosa, which showed strong sensitivity (Figure 4) even at 62.5 g/ml, with a maximal zone of inhibition of 20 mm at 500 g/ml concentration against the test organisms. The least susceptible isolate to the chosen drugs is Staphylococcus epidermidis (Figure 6). In addition to releasing reactive oxygen species like superoxide and aiding in the destruction of biomolecules, aqueous broccoli extract causes a fast deterioration in the integrity of bacterial cell membranes ( 35 , 41 ).

Figure 4. Antibacterial action of Broccoli extract Con. on E. coli

Figure 5. Antibacterial action of Broccoli extract Con. on P. aeruginosa

Figure 6. Antibacterial action on Broccoli extract Con. on S. epidermidis

Figure 7. Antibacterial action of Broccoli extract Con. on S. mutants

In Iraq, broccoli (Brassica oleracea) is a recently introduced crop. It contains chemical properties that might be used in various herbal formulations, including anti-inflammatory, antibacterial, antioxidant, analgesic, antipyretic, heart tonic, and antiasthmatic.

Authors' Contribution

Study concept and design: Z. A. T.

Acquisition of data: M. M. K.

Analysis and interpretation of data: M. M. T.

Drafting of the manuscript: E. S. A.

Critical revision of the manuscript for important intellectual content: H. A. M.

Statistical analysis: C. S. A. I.

Administrative, technical, and material support: Z. A. T.

Conflict of Interest

The authors declare that they have no conflict of interest.

References

  1. Hu SH, Wang JC, Kung HF, Wang JT, Lee WL, Yang YH. Antimicrobial effect of extracts of cruciferous vegetables. Kaohsiung J Med Sci. 2004; 20(12):591-9.
  2. Mahn A, Reyes A. An overview of health-promoting compounds of broccoli (Brassica oleracea var. italica) and the effect of processing. Food Sci Technol Int. 2012; 18(6):503-14.
  3. Owis AI. Broccoli: The Green Beauty: a review. J Pharm Sci Res. 2015; 7(9):696-703.
  4. Pacheco-Cano RD, Salcedo-Hernandez R, Lopez-Meza JE, Bideshi DK, Barboza-Corona JE. Antimicrobial activity of broccoli (Brassica oleracea var. italica) cultivar Avenger against pathogenic bacteria, phytopathogenic filamentous fungi and yeast. J Appl Microbiol. 2018; 124(1):126-35.
  5. Park SK, Ha JS, Kim JM, Kang JY, Lee du S, Guo TJ, et al. Antiamnesic Effect of Broccoli (Brassica oleracea var. italica) Leaves on Amyloid Beta (Abeta)1-42-Induced Learning and Memory Impairment. J Agric Food Chem. 2016; 64(17):3353-61.
  6. Vinha AF, Alves RC, Barreira SV, Costa AS, Oliveira MB. Impact of boiling on phytochemicals and antioxidant activity of green vegetables consumed in the Mediterranean diet. Food Funct. 2015; 6(4):1157-63.
  7. Yang Y, Zhang X. In vitro antitumor activity of broccolini seeds extracts. Scanning. 2011; 33(6):402-4.
  8. Vinodh K, Natarajan A, Devi K, Senthilkumar B. Chemical composition of aqueous leaf extract of Murraya Koenigii. Int J Pharm Biol Archiv. 2013; 4:493-7.
  9. Gani A. Chemical constituents and uses, medicinal plants of Bangladesh. Asiat Soc Bangladesh. 2003; 434
  10. Fernie AR, Trethewey RN, Krotzky AJ, Willmitzer L. Metabolite profiling: from diagnostics to systems biology. Nat Rev Mol Cell Biol. 2004; 5(9):763-9.
  11. Kinnula VL, Crapo JD. Superoxide dismutases in malignant cells and human tumors. Free Radic Biol Med. 2004; 36(6):718-44.
  12. Sas K, Robotka H, Toldi J, Vecsei L. Mitochondria, metabolic disturbances, oxidative stress and the kynurenine system, with focus on neurodegenerative disorders. J Neurol Sci. 2007; 257(1-2):221-39.
  13. Singh U, Jialal I. Oxidative stress and atherosclerosis. Pathophysiology. 2006; 13(3):129-42.
  14. Arteel GE. Oxidants and antioxidants in alcohol-induced liver disease. Gastroenterology. 2003; 124(3):778-90.
  15. Bolton JL, Trush MA, Penning TM, Dryhurst G, Monks TJ. Role of quinones in toxicology. Chem Res Toxicol. 2000; 13(3):135-60.
  16. Guidi I, Galimberti D, Lonati S, Novembrino C, Bamonti F, Tiriticco M, et al. Oxidative imbalance in patients with mild cognitive impairment and Alzheimer's disease. Neurobiol Aging. 2006; 27(2):262-9.
  17. Hyun DH, Hernandez JO, Mattson MP, de Cabo R. The plasma membrane redox system in aging. Ageing Res Rev. 2006; 5(2):209-20.
  18. Martysiak-Żurowska D, Wenta W. A comparison of ABTS and DPPH methods for assessing the total antioxidant capacity of human milk. Acta Sci Pol Technol Aliment. 2012; 11(1):83-9.
  19. Ramakrishna BS, Varghese R, Jayakumar S, Mathan M, Balasubramanian KA. Circulating antioxidants in ulcerative colitis and their relationship to disease severity and activity. J Gastroenterol Hepatol. 1997; 12(7):490-4.
  20. Rimm EB, Ascherio A, Giovannucci E, Spiegelman D, Stampfer MJ, Willett WC. Vegetable, fruit, and cereal fiber intake and risk of coronary heart disease among men. JAMA. 1996; 275(6):447-51.
  21. Rimm EB, Katan MB, Ascherio A, Stampfer MJ, Willett WC. Relation between intake of flavonoids and risk for coronary heart disease in male health professionals. Ann Intern Med. 1996; 125(5):384-9.
  22. Smith MA, Rottkamp CA, Nunomura A, Raina AK, Perry G. Oxidative stress in Alzheimer’s disease. Biochim Biophys Acta Mol Basis Dis Bba-Mol Basis Dis. 2000; 1502(1):139-44.
  23. Upston JM, Kritharides L, Stocker R. The role of vitamin E in atherosclerosis. Prog Lipid Res. 2003; 42(5):405-22.
  24. Eberhardt MV, Lee CY, Liu RH. Antioxidant activity of fresh apples. Nature. 2000; 405(6789):903-4.
  25. Ganesan K, Kumar KS, Rao PVS. Comparative assessment of antioxidant activity in three edible species of green seaweed, Enteromorpha from Okha, Northwest coast of India. Innov Food Sci Emerg Technol. 2011; 12(1):73-8.
  26. Michaud DS, Spiegelman D, Clinton SK, Rimm EB, Willett WC, Giovannucci EL. Fruit and vegetable intake and incidence of bladder cancer in a male prospective cohort. J Natl Cancer Inst. 1999; 91(7):605-13.
  27. Rose P, Huang Q, Ong CN, Whiteman M. Broccoli and watercress suppress matrix metalloproteinase-9 activity and invasiveness of human MDA-MB-231 breast cancer cells. Toxicol Appl Pharmacol. 2005; 209(2):105-13.
  28. Singh AV, Xiao D, Lew KL, Dhir R, Singh SV. Sulforaphane induces caspase-mediated apoptosis in cultured PC-3 human prostate cancer cells and retards growth of PC-3 xenografts in vivo. Carcinogenesis. 2004; 25(1):83-90.
  29. Sivakumar S. Therapeutic potential of chitosan nanoparticles as antibiotic delivery system: challenges to treat multiple drug resistance. Asian J Pharm. 2016; 10(2)
  30. Dhandevi P, Jeewon R. Fruit and vegetable intake: Benefits and progress of nutrition education interventions-narrative review article. Iran J Public Health. 2015; 44(10):1309.
  31. Liu RH. Dietary bioactive compounds and their health implications. J Food Sci. 2013; 78(1):18-25.
  32. Murphy MM, Barraj LM, Spungen JH, Herman DR, Randolph RK. Global assessment of select phytonutrient intakes by level of fruit and vegetable consumption. Br J Nutr. 2014; 112(6):1004-18.
  33. Chaudhary A, Rampal G, Sharma U, Thind TS, Singh B, Vig AP, et al. Anticancer, antioxidant activities and GC-MS analysis of glucosinolates in two cultivars of broccoli. Med Chem Drug Disc. 2012; 2(2):30-7.
  34. Abdulazeem L, AL-Amiedi BH, Alrubaei HA, AL-Mawlah YH. Titanium dioxide nanoparticles as antibacterial agents against some pathogenic bacteria. Drug Invent Today. 2019; 12(5):963-7.
  35. CLSI. Performance standards for Antimicrobial Susceptibility Testing Texas: Clinical and Laboratory Standards Institute: CLSI Document M02-A10 andM07-A8; 2012.
  36. CLSI. Performance Standards for Antimicrobial SusceptibilityTesting Wayne, PA: Clinical and Laboratory Standards Institute: CLSI Supplement M100S; 2020.
  37. Abdulazeem L, Al-Jassani M, Al-Sheakh M. Free Radical Scavenging and Antioxidant Activity of Silver Nanoparticles Synthesized from Cuminum cyminum (Cumin) seed Extract. Res J Pharm Technol. 2021;4349-54.
  38. Wang W, Chen Q, Jiang C, Yang D, Liu X, Xu S. One-step synthesis of biocompatible gold nanoparticles using gallic acid in the presence of poly-(N-vinyl-2-pyrrolidone). Colloids Surf A: Physicochem Eng Asp. 2007; 301(1):73-9.
  39. Awika JM, Rooney LW, Wu X, Prior RL, Cisneros-Zevallos L. Screening methods to measure antioxidant activity of sorghum (sorghum bicolor) and sorghum products. J Agric Food Chem. 2003; 51(23):6657-62.
  40. Chang ST, Wu JH, Wang SY, Kang PL, Yang NS, Shyur LF. Antioxidant activity of extracts from Acacia confusa bark and heartwood. J Agric Food Chem. 2001; 49(7):3420-4.
  41. Kim S-C, Lee D-K. Preparation of TiO2-coated hollow glass beads and their application to the control of algal growth in eutrophic water. Microchem J. 2005; 80(2):227-32.