Biology:Murashige and Skoog medium
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Murashige and Skoog medium (or MSO or MS0 (MS-zero)) is a plant growth medium used in the laboratories for cultivation of plant cell culture. MS0 was invented by plant scientists Toshio Murashige and Folke K. Skoog in 1962 during Murashige's search for a new plant growth regulator. A number behind the letters MS is used to indicate the sucrose concentration of the medium. For example, MS0 contains no sucrose and MS20 contains 20 g/L sucrose. Along with its modifications, it is the most commonly used medium in plant tissue culture experiments in the laboratory.[1] However, according to recent scientific findings, MS medium is not suitable as a nutrient solution for deep water culture or hydroponics.[2]
As Skoog's doctoral student, Murashige originally set out to find an as-yet undiscovered growth hormone present in tobacco juice. No such component was discovered; instead, analysis of juiced tobacco and ashed tobacco revealed higher concentrations of specific minerals in plant tissues than were previously known. A series of experiments demonstrated that varying the levels of these nutrients enhanced growth substantially over existing formulations. It was determined that nitrogen in particular enhanced growth of tobacco in tissue culture.
Ingredients
Major salts (macronutrients) per litre
- Ammonium nitrate (NH4NO3) 1650 mg/l
- Calcium chloride (CaCl2 · 2H2O) 440 mg/l
- Magnesium sulfate (MgSO4 · 7H2O) 180.7 mg/l
- Monopotassium phosphate (KH2PO4) 170 mg/l
- Potassium nitrate (KNO3) 1900 mg/l.
Minor salts (micronutrients) per litre
- Boric acid (H3BO3) 6. 2 mg/l
- Cobalt chloride (CoCl2 · 6H2O) 0.025 mg/l
- Ferrous sulfate (FeSO4 · 7H2O) 27.8 mg/l
- Manganese(II) sulfate (MnSO4 · 4H2O) 22.3 mg/l
- Potassium iodide (KI) 0.83 mg/l
- Sodium molybdate (Na2MoO4 · 2H2O) 0.25 mg/l
- Zinc sulfate (ZnSO4·7H2O) 8.6 mg/l
- Ethylenediaminetetraacetic acid ferric sodium (FeNaEDTA) 36.70 mg/L
- Copper sulfate (CuSO4 · 5H2O) 0.025 mg/l
Vitamins and organic compounds per litre
- Myo-Inositol 100 mg/l
- Nicotinic Acid 0.5 mg/l
- Pyridoxine · HCl 0.5 mg/l
- Thiamine · HCl 0.1 mg/l
- Glycine 2 mg/l
- Tryptone 1 g/l (optional)
- Indole Acetic Acid 1-30 mg/l (optional)
- Kinetin 0.04-10 mg/l (optional)
See also
- Hoagland solution
- Long Ashton Nutrient Solution
References
- ↑ Trigiano, Robert N.; Gray, Dennis J. (2010). Plant Tissue Culture,Development and Biotechnology. Boca Raton: CRC Press. pp. 186. ISBN 978-1-4200-8326-2.
- ↑ van Delden, S.H.; Nazarideljou, M.J.; Marcelis, L.F.M. (2020). "Nutrient solutions for Arabidopsis thaliana: a study on nutrient solution composition in hydroponics systems". Plant Methods 16 (72): 1–14. doi:10.1186/s13007-020-00606-4. PMID 32612669.
- Murashige, T; Skoog, F (1962). "A Revised Medium for Rapid Growth and Bio Assays with Tobacco Tissue Cultures". Physiologia Plantarum 15 (3): 473–497. doi:10.1111/j.1399-3054.1962.tb08052.x.
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