Next Article in Journal
Effect of Quercetin on Paraoxonase 2 Levels in RAW264.7 Macrophages and in Human Monocytes—Role of Quercetin Metabolism
Previous Article in Journal
Binding and Docking Interactions of NO, CO and O2 in Heme Proteins as Probed by Density Functional Theory
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Lysis of Microcystis aeruginosa with Extracts from Chinese Medicinal Herbs

1
Key Lab of Food Quality and Safety of Jiangsu Province, Jiangsu Academy of Agricultural Sciences, Nanjing 210014, China
2
School of Food, Henan Institute of Science and Technology, Xinxiang 453003, China
*
Author to whom correspondence should be addressed.
Int. J. Mol. Sci. 2009, 10(9), 4157-4167; https://doi.org/10.3390/ijms10094157
Submission received: 17 August 2009 / Revised: 10 September 2009 / Accepted: 21 September 2009 / Published: 23 September 2009
(This article belongs to the Section Biochemistry)

Abstract

:
Boiling water extracts of 66 selected Chinese medicinal herbs were screened for their anticyanobaterial activity against Microcystis aeruginosa by the soft-agar overlayer (SAO) method. Results indicated that extracts from 16 materials could inhibit the growth of this bacterial species. Among these anticyanobacterial samples, eight extracts showed low minimum inhibitory concentrations (MIC), including four extracts with MICs between 1 and 6 mg/mL, and four extracts with MICs < 1 mg/mL which could be considered useful to prevent the outbreak of cyanobacteria before the appearance of cyanobacterial blooms. Further study showed that three extracts with MIC values < 1 mg/mL induced intensive chlorophyll-a lysis within 7 days at the MIC. The results suggested that highly efficient anticyanobacterial compounds must be involved in the inhibitory activities. The final results indicated these three extracts (from Malaphis chinensis, Cynips gallae-tinctoriae and Fructus mume) had the potential to be developed as algicides due to their remarkably anticyanobacterial activities.

Graphical Abstract

1. Introduction

Cyanobacteria (blue-green algae) are photoautotrophic Gram-negative bacteria which commonly evoke occurrence of blooms and scums in lakes, reservoirs, slow-flowing rivers [1]. Due to their musty odor and production of potent toxins, cyanobacteria populations are a great concern in reservoir supplies and recreational water systems [2]. Microcystis aeruginosa, found globally in fresh waters, is a cyanobacterium which can produce toxins threatening public health [3], so M. aeruginosa has been the subject of increasing research over the last decades. To minimize the threat, methods of prevention and control for bloom problems have been adopted, such as chemical treatments with algaecides [4] and biological control [5]. Algicidal compounds are widely used in industrial waters, for the sanitation of swimming pools and the like. Copper sulfate, chelated copper compounds, and diuron (3-[3,4-dichlorophenyl]-1,1-dimethylurea) are the only compounds currently approved by the U.S. Environmental Protection Agency for use as algicides in catfish production ponds. Unfortunately, these compounds have the following undesirable characteristics: (i) broad-spectrum toxicity towards phytoplankton that can result in the death of the entire phytoplankton community and subsequent water quality deterioration that may stress or kill catfish; (ii) lengthy persistence in the environment that creates concerns about environmental safety; and (iii) the public’s negative perception of the use of synthetic herbicides in food fish production ponds [6]. Ideally, in the concentration employed, they should be harmless for man and animals.
Thousands of plants worldwide are used in traditional medicine as treatments for bacterial infections and especially traditional Chinese medicinal herbs which contain abundant potential antimicrobial agents have been used for the treatment of a wide variety of diseases for thousands of years [7]. In recent years, screening of plant resources for antimicrobial compounds has being intensively carried on worldwide, but there has been no screening of Chinese herbs extracts against M. aeruginosa.
In this study, we aimed to investigate potential useful plant compounds or extracts from Chinese herbs which should ideally display lysis activity against cyanobacteria. We expect that this study will contribute to the control of pollution by M. aeruginosa and the following identification of active compounds for emergencies caused by this species.

2. Results and Discussion

2.1. Results

2.1.1. Anticyanobacterial Screening

By the SAO method, diverse levels of anticyanobacterial activities were observed in the plates containing different tested extracts. The final screening results are listed in Table 1. Generally, it was found that extracts from 16 materials showed inhibitory activity towards M. aeruginosa. Among the 16 extracts, Herba Patriniae, Forsythia suspensa (Thunb.) Vahl, Rubia cordifolia, Polygala tenuifolia, Acorus tatarinowii, Sophora flavescens, Rhizoma Chuanxiong, Rhizoma Corydalis and Ranunculus ternatus extracts showed low inhibition levels to M. aeruginosa with DIZ (diameter of inhibition zone) values ≥ 10 mm; Fraxinus rhynchophylla, Crataegus pinnatifida, and Euphorbia humifusa extracts showed moderate levels of activity, with DIZ values ≥ 20 mm; Cornus officinalis Sieb. et Zucc, Malaphis chinensis, Cynips gallae-tinctoriae and Fructus mume extracts showed high activity levels, withDIZ values ≥ 30 mm.

2.1.2. Determination of M. aeruginosa-Inhibiting Abilities of 16 Selected Chinese Herbs Extracts

The inhibitory abilities of selected Chinese herbs extracts were confirmed by determining the MIC towards M. aeruginosa. All the results wre listed in Table 2. Extracts of C. gallae-tinctoriae, M. chinensis, F. mume, Herba Patriniae exhibited the lowest MIC values (<1 mg/mL); The MIC values of C. pinnatifida, C. officinalis Sieb. Et, F. rhynchophylla, E. humifusa are all at 3.125 mg/mL. MIC values of the remaining eight extracts were all higher than 6 mg/mL, which meant their M. aeruginosa-inhibiting abilities were very low and so they were excluded in the sebsequent study.

2.1.3. Dynamic Analysis of Chlorophyll-a in M. aeruginosa with Remained 8 Chinese Herbs Extracts

Changes of the chlorophyll a (Chl-a) contents of the M. aeruginosa in a sterile BG11 culture solution for seven days were recorded as a time course curve (Figure 1). Effects of the eight finally selected Chinese herbs extracts on the M. aeruginosa growth could be observed from corresponding curve. Generally speaking, each extract finally caused the Chl-a lysis of M. aeruginosa, but their lysing actions differed with regards to the inception time and efficacy. From Figure 1, it is seen that except for treatment with P. mume extract, the Chl-a of all treated M. aeruginosa started lysing two days after the inoculation of tested extracts. C. gallae-tictoriae, M. chinensis, C.officinalis Sieb. Et and F. mume extracts almost induced Chl-a complete lysis in seven days (Figures 1 a–d). However, F. rhynchophylla, E. humifusa, C. pinnatifida and H. Patriniae extracts only induced partial lysis of Chl-a in seven days (Figures 1 e–h).

2.2. Discussion

China has a rich flora that is widely distributed throughout the country. Chinese medicinal herbs have been the basis of treatment and cure for various diseases and physiological conditions in traditional methods. In fact, many naturally occurring compounds found in plants, herbs, and spices have been shown to possess antimicrobial functions and serve as sources of antimicrobial agents against foodborne pathogens [8]. In this study, it was indicated that many extracts from selected Chinese medicinal herbs possessed ideal inhibition activity against cyanobacteria.
The SAO method was employed for screening the anticyanobacterial Chinese herbs. Anticyanobacterial activity was evaluated by measuring the DIZ of the tested cyanobacterium. In such tests, extracts containing active insolvable compounds would escape detection, but considering the potential applications, it was preferred to focus on the extracts containing active soluble compounds. Solubility and diffusion of active components in agar media could play a major role in the formation of inhibition zone, which suggested that DIZ might not be absolutely equivalent to the anticyanobacterial capability, hence the MIC values of all positive extracts screened by SAO were determined to evaluate their anticyanobacterial capability. Extracts of C. gallae-tinctoriae, M. chinensis, F. mume, and H. Patriniae exhibited low MIC values (<1 mg/mL), which indicated their potential to be timely applied to prevent the outbreak of cyanobacteria before the occurrence of cyanobacterial bloom.
The M. aeruginosa-lytic activity of the selected extracts was evaluated for their potential as algicides. It was found that extracts of C. gallae-tinctoriae, M. chinensis, F. mume and C. officinalis Sieb. Et showed obvious lytic activity towards M. aeruginosa, while extract of H. Patriniae showed too weak lytic activity to be a useful algicide. Considering the far higher MIC and average M. aeruginosa-lytic activity, the extract of C.officinalis Sieb Et was not recommend for development as an algicide. It should be noted that the initial time for lytic actions of these extracts were different at their MICs, and F.mume extract exhibited fast acting lysis activity against Chl-a of M. aeruginosa which was different from other extracts. These results suggested that P. mume extract probably contained some special active compounds involved in the lysis of M. aeruginosa, and such extract could be considered as acute algaecide applied in some emergencies caused by M. aeruginosa.
Many volatile organic compounds have been found to have lytic activity against cyanobacteria. It was confirmed that volatile terpenoid compounds produced by plants had lytic activity [9]. According to Cowan [10], aqueous plant extracts mainly contain anthocyanins, starches, tannins, saponins, terpenoids, polypeptides, lectins, etc, so Chinese herbs extracts could be expected to have universal anticyanobacteria activity, but this was not really the case. Many extracts did not display any anticyanobacteria activity. Therefore, it was implied that the content of the active ingredients was different in different Chinese medicinal herbs. For instance, the aqueous extracts of F. mume mainly contain organic acids, terpenoids, sterols, flavonoids, carbohydrates and amino acids. Especially, the concentration of organic acids was very high (up to 40.5%) [11]. Malic acid and citric acid were the major organic acid constituents, while ethanedioic acid, glycolic acid, lactic acid, succinic acid, formic acid, acetic acid, propionic acid, etc were also present. Lots of these organic acids have been reported to have inhibition activity towards some microbe species [1214], so it was very likely that these organic acids induce the lysis of cyanobacteria. Of course, terpenoids (ursolic acid) and flavonoids may show synergistic effect on the growth of cyanobacteria. In addition, some amino acids (e.g., lysine, histidine, alanine) may also accelerate the lysis of cyanobacteria [15]. M. chinensis is a traditional Chinese herb distributed widely in southern China. It is the gallae that is produced by some parasitic aphids (family Pemphigidae) on Rhus leaves of the family Anacardiaceae (mainly Rhus chinensis Mill, Rhus potaninii Maxim, and Rhus punjabensis var. sinica (Diels) Rehd. et Wils) [16]. The surface feature of C. gallae-tinctoriae is very similar to M. chinensis. Both of them are gallae, and the active compounds from their aqueous extracts should be also similar, containing a large amount of gallotannin, a typical hydrolysable tannin, with the content of up to 70% of its weight [17]. The content of gallic acid in the extract is about 2%~4%. It was reported that gallotannin and gallic acid could inhibit the growth of intestinal bacteria [18], so it was presumed that gallotannin and gallic acid were at least partially responsible for the observed lysis of cyanobacteria by the extracts from M. chinensis or C. gallae-tinctoriae. Even the active extracts showed diverse levels in efficiency and inception time. The results indicated that multiple and diverse active compounds with anticyanobacteria activity existed in the extracts. It would be of interest to purify and identify the responsible bioactive components from these extracts.

3. Experimental Section

3.1. Cyanobacteria Culture and Chinese Medicinal Herbs

M.aeruginosa (FACHB 905) was obtained from the Freshwater Algae Culture Collection of the Institute of Hydrobiology (FACHB), located in China. The strain was grown in BG-11 medium [19] at 25 °C with illumination at 3,000 lx under a 16 L/8 D cycle. Sixty-six Chinese medicinal herbs were obtained from traditional medicine stores in Nanjing. The different parts of the plant used were the leaves, the branches, the fruits, the rhizomes, the peels, the gallaes shown in Tables 1 and 2.

3.2. Preparation of the Extracts

Stock solutions were prepared with the traditional process currently used in Chinese clinics and scientific studies by boiling 100 g of raw material with 1,000 mL of distilled water for 1 h. The material was centrifuged and filtered through filter paper. The residue remaining on the filter paper was reboiled with 1,000 mL distilled water, centrifuged, and refiltered. The resulting two batches of the solution were mixed and then boiled again until 100 mL remained. This solution was regarded as a concentration of 100% (100 mL of HC solution made from 100 g of raw material). After being autoclaved, the stock solution was stored at 4 °C until used.

3.3. Measurement of Anticyanobacterial Activity

The anticynobacterial activity was determined using the soft-agar overlayer (SAO) method [20]. Approximately 5 mL of cyanobacterial cells (2 × 106 cells/mL) were mixed with warmed 5 mL of 0.8% (w/v) soft agar and over-layered on a 10 mL of 1.2% (w/v) agar layer solidified in a plate. After the cyanobacterium containing layer was solidified. Sterilized Oxford cups (8 mm in external diameter) were put up on the cyanobacterium-containing layer regularly and 200 μL extract solutions were respectively deposited on the disc, and the concentration of the test herb extracts were diluted to 200 mg/mL. 20 μg/mL CuSO4 and distilled water were used as positive and negative controls, respectively. The plates were incubated at 25 °C for 2 days. Anticyanobacterial activity was evaluated by measuring the diameter of inhibition zone (DIZ) of the tested cynobacterium. DIZ was expressed in millimeters. All tests were performed in triplicate.

3.4. Determination of Minimum Inhibitory Concentration (MIC)

Several anticynobacterial extracts were screened from the material extracts by disc diffusion method. A broth microdilution method was used to determine the MIC [21,22]. An aliquot of 0.1 mL of a serially diluted Chinese herb extracts in BG11 medium was added to a 96-well microplate and 0.1 mL of cyanobacteria cultured broth (2 × 106 cells/mL) was added to each well. Then the resulting solution was incubated at 25 °C under 3,000 lx continuous illumination for a week. The MIC is defined as the lowest concentration of the extracts at which the cynobacteria does not demonstrate visible growth. Each test was performed in triplicate.

3.5. Extraction and Measurement of Cyanobacterial Chlorophyll a

A solution of 90% methanol was used for extraction of chlorophyll a (chl-a) from cyanobacteria. Measurement of chl-a was according to the method of Parsons and Strickland [23]. Cyanobacteria collected by centrifugation (12,000 r.p.m., 15 min, 4 °C) were subjected to extraction with 90% methanol in a water bath (60 °C) for 10 min. After extraction, the solid suspension was removed by centrifugation (12,000 r.p.m., 15 min, 4 °C). Then, the absorbance of extracts at 665, 645 and 635 nm was measured using a spectrophotometer (Perkin Lambda 25). The concentration of chl-a was calculated using the following equation [15]: Chl-a (μg/mL) = 11.6A665-1.31A645-0.14A635.

4. Conclusions

In this study, it was indicated that many Chinese herbs possess anticyanobanteria activity. Our results showed that C. gallae-tinctoriae, M. chinensis, and F. mume have potential as algicides due to their remarkable anticyanobacterial effects.

Acknowledgments

This work was supported by the Special Project of National Grand Fundamental Research Pre-973 Program of China under Grant No. 2008CB117001.

References and Notes

  1. Chow, CWK; House, J; Velzeboer, RMA; Drikas, M; Burch, MD; Steffensen, DA. The effect offerricc hloride flocculation on cyanobacterial cells. Water Res 1998, 32, 808–814. [Google Scholar]
  2. Codd, GA; Bell, SG; Kaya, K; Ward, CJ; Beattie, KA; Metcalf, JS. Cyanobacterial toxins, exposure routes and human health. Eur J Phycol 1999, 34, 405–415. [Google Scholar]
  3. Reynolds, CS; Walsby, AE. Water blooms. Biol Res 1975, 50, 437–481. [Google Scholar]
  4. Hrudey, S; Burch, S; Burch, M; Drikas, M; Greorgy, R. Toxic cyanobacteria in water, a guide to their public health consequences, monitoring and management. In Remedial Measures; Chorus, I, Bartram, J, Eds.; Routledge: London, UK, 1999; pp. 275–312. [Google Scholar]
  5. Choi, HJ; Kim, BH; Kim, JD; Han, MS. Streptomyces neyagawaensis as a control for the hazardous biomass of Microcystis aeruginosa (Cyanobacteria) in eutrophic freshwaters. Biol Control 2005, 33, 335–343. [Google Scholar]
  6. Schrader, KK; Nanayakkara, NPD; Tucker, CS; Rimando, AM; Ganzera, M; Schaneberg, BT. Novel derivatives of 9,10-anthraquinone are selective algicides against the musty-odor cyanobacterium Oscillatoria perornata. Appl. Environ. Microbiol 2003, 69, 5319–5327. [Google Scholar]
  7. Bensky, D; Gamble, A. Chinese herbal medicine. In Materia Medica; Rev edEastland Press, Inc: Seattle, WA, USA, 1993; pp. 13–17. [Google Scholar]
  8. Deans, SG; Ritchie, GA. Antimicrobial properties of plant essential oils. Int. J. Food Microbiol 1987, 5, 165–180. [Google Scholar]
  9. Ozaki, K; Ohta, A; Iwata, C; Horikawa, A; Tsuji, K; Ito, E; Ikai, Y; Harada, KI. Lysis of cyanobacteria with volatile organic compounds. Chemosphere 2008, 7, 1531–1538. [Google Scholar]
  10. Cowan, MM. Plant products as antimicrobial agents. Clin. Microbiol. Rev 1999, 12, 564–582. [Google Scholar]
  11. Shen, HM; Qiao, CZ; Su, ZW. Quantitative dynamic analysis of the main component of organic acid in the Fructus mume. Chin. Pharmaceu. J 1995, 30, 133–135. [Google Scholar]
  12. Nikolaus, BE; Wayman, BE; Encinas, E. The bactericidal effect of citric acid and sodium hypochlorite on anaerobic bacteria. J. Endod 1988, 14, 31–34. [Google Scholar]
  13. Georgopoulou, M; Kontakiotis, E; Nakou, M. Evaluation of the antimicrobial effectiveness of citric acid and sodium hypochlorite on the anaerobic flora of the infected root canal. Int. Endod. J 1994, 27, 139–143. [Google Scholar]
  14. Greer, GG; Dilts, BG. Lactic acid inhibition of the growth of spoilage bacteria and cold tolerant pathogens on pork. Int. J. Food Microbiol 1995, 25, 141–151. [Google Scholar]
  15. Takamura, Y; Yamada, T; Kimoto, A; Kanehama, N; Tanaka, T; Nakadaira, S; Yagi, O. Growth inhibition of microcystis cyanobacteria by l-lysine and disappearance of natural microcystis blooms with spraying. Microb Environ 2004, 19, 31–39. [Google Scholar]
  16. Tian, F; Li, B; Ji, BP; Yang, JH; Zhang, GZ; Chen, Y; Luo, YC. Antioxidant and antimicrobial activities of consecutive extracts from Galla chinensis: The polarity affects the bioactivities. Food Chem 2009, 113, 173–179. [Google Scholar]
  17. Sun, DW. Chemistry of Vegetable Tannins (in Chinese); Chinese Forest Press: Beijing, China, 1992; Chapter 1pp. 257–260. [Google Scholar]
  18. Ahn, YJ; Lee, CO; Kweon, JH; Ahn, JW; Park, JH. Growth-inhibitory effects of Galla Rhois-derived tannins on intestinal bacteria. J. Appl. Microbiol 1998, 84, 439–443. [Google Scholar]
  19. Stanier, R; Kunisawa, R; Mandel, M; Cohen-Bazire, G. Purification and properties of unicellular blue-green algae (Order Chroococcales). Bacteriol Rev 1971, 35, 171–205. [Google Scholar]
  20. Uchida, H; Kouchiwa, T; Watanabe, K; Kawasaki, A; Hodoki, Y; Otani, I; Yamamoto, Y; Suzuki, M; Harada, KI. A coupled assay system for the lysis of cyanobacteria. Jpn J Water Treat Biol 1998, 34, 67–75. [Google Scholar]
  21. National Committee for Clinical Laboratory Standards (NCCLS). Performance Standards for Antimicrobial Susceptibility Test, Ninth International Supplement. M100-S9; NCCLS: Wayne, PA, USA, 1999. [Google Scholar]
  22. Bassole, IHN; Quattara, AS; Nebie, R; Quattara, CAT; Kabore, ZI; Traore, SA. Chemical composition and antibacterial activities of the essential oils of Lippia chevalieri and Lippia multiflora from Burkina Faso. Phytochemistry 2003, 62, 209–212. [Google Scholar]
  23. Parsons, TR; Strickland, JDH. Discussion of spectrophotometric determination of marine-plant pigments, with revised equations for ascertaining chlorolphylls and carotenoids. J. Mar. Res 1963, 21, 155–163. [Google Scholar]
Figure 1. Effects of different Chinese herbs extracts on the contents of chlorophyll a at MIC value. Control: M.aeruginosa (▪); Treat: Chinese herbs extracts (•) [a: C.gallae-tictoriae (0.39 mg/mL); b: M.chinensis (0.39 mg/mL); c: C.officinalis Sieb. Et (3.125 mg/mL); d: F. mume (0.78 mg/mL); e: F.rhynchophylla (3.125 mg/mL); f: E.humifusa (3.125 mg/mL); g: C.pinnatifida (3.125 mg/mL); h: H. Patriniae (0.78 mg/mL)]. Each point represents mean ±SE of three replications.
Figure 1. Effects of different Chinese herbs extracts on the contents of chlorophyll a at MIC value. Control: M.aeruginosa (▪); Treat: Chinese herbs extracts (•) [a: C.gallae-tictoriae (0.39 mg/mL); b: M.chinensis (0.39 mg/mL); c: C.officinalis Sieb. Et (3.125 mg/mL); d: F. mume (0.78 mg/mL); e: F.rhynchophylla (3.125 mg/mL); f: E.humifusa (3.125 mg/mL); g: C.pinnatifida (3.125 mg/mL); h: H. Patriniae (0.78 mg/mL)]. Each point represents mean ±SE of three replications.
Ijms 10 04157f1
Table 1. Anticynobacterial activity of various extracts with boiling water by the disc diffusion method.
Table 1. Anticynobacterial activity of various extracts with boiling water by the disc diffusion method.
Botanical nameEnglish namePart testedM.aeruginosa
ControlN
P++
Cornus officinalis Sieb. et ZuccMedical DogwoodFruit+++
Malaphis chinensisGallnutGallae+++
Fructus mumeSmoked PlumFruit+++
Cynips gallae-tinctoriae OlivierNutgallGallae+++
Euphorbia humifusa WilldHumifuse SpurgeWhole plant++
Fraxinus rhynchophylla HanceAsh BarkPeel++
Crataegus pinnatifidaHawthornFruit++
Rubia cordifolia Linn.India Madder RootWhole plant+
Polygala tenuifolia WilldThinleaf Milkwort RootWhole plant+
Acorus tatarinowii SchottRhizoma Acori TatarinowiiWhole plant+
Sophora flavescens AltLightyellow Sophora RootRhizome+
Rhizoma ChuanxiongLigusticum Chuanxiong HortRhizome+
Rhizoma CorydalisYanhusuoWhole plant+
Forsythia suspensa (Thunb.) VahlWeeping ForsythiaWhole plant+
Herba PatriniaeWhite flower Patrinia HerbWhole plant+
Ranunculus ternatus ThunbRadix Ranunculi TernatiWhole plant+
Eichhornia crassipes (Mart.) SolmsWeter HyacinthBranch
Suaeda glauca BgeCommon Seepweed HerbWhole plant
Houttuynia cordata ThuhbHerba HouttuyniaeWhole plant
Isatis tinctoria LIsatis RootRhizome
Herba TaraxaciDandelionWhole plant
Pulsatilla chinensis (Bunge) RegelAnemoneWhole plant
CoptischinensisFranchCoptis ChinensisWhole plant
Folium IsatidisFolium IsatidisLeaf
Prunella vulgarisSpica PrunellaeWhole plant
Punica granatumPomegranatePeel
Terminalia chebula RetzMedicine Terminalia FruitFruit
Gardenia: jasminoides EllisCape JasmineFruit
Viola philippica ssp.munda W. BeckPurple flower VioletLeaf
Anemarrhena asphodeloides BungeCommon Rhizoma AnemarrhenaeFruit
Rhizoma CyperiNutgrass Galingale RhizomFruit
Lithospermum erythrorhizon Sieb.et ZuccGromwell RootWhole plant
Herba Artemisiae AnnuaeSweet Wormwood HerbWhole plant
Zanthoxylum bungeanumPricklyash PeelFruit
Aucklandia lappa Decne.Radix AucklandiaeRhizome
Glycyrrhiza uralensis FischLicorice Roots Northwest OriginWhole plant
Rhizoma Smilacis GlabraeGlabrous Greenbrier RhizomeRhizome
Sanguisorba officinalis LinnGarden BurnetRhizome
Pericarpium Citri ReticulataeDried Tangerine peelpeel
Herba Senecionis ScandentisClimbing Groundsel HerbWhole plant
Schisandra chinensis (Turcz.) BaillChinese Magnolivine FruitFruit
Clematis chinensis OsbeckRadix ClematidisWhole plant
Drynaria fortunei (Kunze) J. SM--Rhizome
Benincasa hispide ThunbWhite gourdPeel
Astragalus membranaceus (Fisch.) BungeAstragaliRhizome
Bupleurum chinense DCBupleuriRhizome
Geranium wilfordii MaximHerba erodiiWhole plant
Subgen. Tsutsusi (G. Don) PojarkovaLoquatLeaf
Cortex Cinnamomi CassiaeCinnamonRhizome
Andrographis paniculata(Burm.f.) NeesCommon Andrographis HerbWhole plant
Lonicera japonica ThunbFlos LoniceraeFlower
Tradescantia albiflora--Whole plant
Portulaca oleracea LinnPurslaneWhole plant
Plantago asiatica LplantainWhole plant
Trachelospermum jasminoides (Lindl.)LemCaulis TrachelospermiWhole plant
Semen CassiaeCassia SeedSeed
Pogostemon cablin (Blanco) BenthAgastache rugosaWhole plant
Folium llicis LatifoliaeBroadleaf Holly leafLeaf
Cyrtomium fortunei J. SmCyrtomii RhizomaRhizome
Herba Menthae HeplocalycisWild Mint HerbLeaf
Syzygium aromaticum (L.) Merr. Et PerryFlos CaryophyllataLeaf
Platycladus orientalis (Linn.)FrancoArborvitaeLeaf
Magnolia liliiflora DesrFlos MagnoliaeFruit
Areca catechu LinnBetel nutPeel
Dryobalanops aromatica Gaertn. f.BorneolResin
Sterculia lychnophera HanceBoat-fruited Sterculia SeedFruit
Gynostemma pentaphyllum Thunb. MakinoFiveleaf Gynostemma HerbLeaf
Reynoutria japonica HouttRhizoma Polygoni CuspidatiLeaf
Abbreviations: N, negative control (distilled water); P, positive control (CuSO4 20 μg/mL); Grading of results: +++, complete inhibition (DIZ: 30~40 mm); ++, moderate inhibition (DIZ: 20~30 mm); +, partial inhibition (DIZ: 10~20 mm); –, no inhibition (DIZ: 8 mm); The outside diameter of oxford cup on the soft-agar overlayer is 8 mm and the diameter of inhibition zone (DIZ) of negative control is also 8 mm. If the DIZ value is 8 mm, that means the extract has no inhibitory activity against M. aeruginosa.
Table 2. MIC values of several chinese herbs against the growth of Microcystis aeruginosa.
Table 2. MIC values of several chinese herbs against the growth of Microcystis aeruginosa.
Botanical nameEnglish namePart testedMIC (mg/mL)
Cynips gallae-tinctoriae OlivierNutgallGallae0.39
Malaphis chinensisgallnuGallae0.39
Herba PatriniaeWhite flower Patrinia HerbWhole plant0.78
Fructus mumeSmoked PlumFruit0.78
Crataegus pinnatifidaNippon Hawthorn FruitFruit3.125
Cornus officinalis Sieb. et ZuccMedical DogwoodFruit3.125
Fraxinus rhynchophylla HanceAsh BarkPeel3.125
Euphorbia humifusa WilldHumifuse SpurgeWhole plant3.125
Forsythia suspensa (Thunb.) VahlWeeping ForsythiaWhole plant6.25
Polygala tenuifolia WilldThinleaf Milkwort RootWhole plant6.25
Rubia cordifolia Linn.India Madder RootWhole plant6.25
Ranunculus ternatus ThunbRadix Ranunculi TernatiWhole plant12.5
Acorus tatarinowii SchottRhizoma Acori TatarinowiiWhole plant12.5
Rhizoma ChuanxiongLigusticum Chuanxiong HortRhizome12.5
Sophora flavescens AltLightyellow Sophora RootRhizome25
Rhizoma CorydalisYanhusuoWhole plant25

Share and Cite

MDPI and ACS Style

Yang, J.-D.; Hu, L.-B.; Zhou, W.; Yin, Y.-F.; Chen, J.; Shi, Z.-Q. Lysis of Microcystis aeruginosa with Extracts from Chinese Medicinal Herbs. Int. J. Mol. Sci. 2009, 10, 4157-4167. https://doi.org/10.3390/ijms10094157

AMA Style

Yang J-D, Hu L-B, Zhou W, Yin Y-F, Chen J, Shi Z-Q. Lysis of Microcystis aeruginosa with Extracts from Chinese Medicinal Herbs. International Journal of Molecular Sciences. 2009; 10(9):4157-4167. https://doi.org/10.3390/ijms10094157

Chicago/Turabian Style

Yang, Jing-Dong, Liang-Bin Hu, Wei Zhou, Yu-Fen Yin, Jian Chen, and Zhi-Qi Shi. 2009. "Lysis of Microcystis aeruginosa with Extracts from Chinese Medicinal Herbs" International Journal of Molecular Sciences 10, no. 9: 4157-4167. https://doi.org/10.3390/ijms10094157

Article Metrics

Back to TopTop