Category: L

  • Lovibond comparator

    Device for the visual comparison of coloured fluid with a series of standards of tinted glass set in a revolving circular wheel, only one of which is opposite to the fluid being evaluated at a given time. Various types of standard are available: in bacteriology the phenol red standards disc is of particular value.  

  • Locke’s solution

    Isotonic suspension medium for bacteria and cells. A mixture of sodium chloride, potassium chloride, calcium chloride and sodium carbonate.  

  • Liver infusion media

    Broth or agar with a peptone – ox liver base, used especially for the cultivation of Brucella. Thionin and basic fuchsin may be included in modifications for differentiating between the various species.  

  • Litmus milk

    Medium for demonstrating lactose femientation, casein digestion or coagulation, and ‘stonny clot’ production in the investigation of clostridial species. Consists of sterile, cream-free milk with alcoholic litmus indicator.  

  • Lithotrophs

    Bacteria able to utilize carbon dioxide as the only source of carbon. Chemolithotrophs derive energy by the oxidation of inorganic compounds, md photolithotrophs from sunlight. Lithotrophic bacteria are non-parasitic.  

  • Liquoid

    Sodium polyethanol sulphate, 0.05 per cent of which may be added to blood culture broth to destroy the natural bactericidal action of blood.  

  • Lipid granules

    Spherical bacillary granules (possibly connected with the storage of carbon and energy) with an affinity for Sudan black or other fat-soluble dyes. The granules appear as blank spaces by Gram or other basic staining methods.  

  • Lindegren’s stain

    Method for volutin granules in bacteria and yeasts. Short or prolonged staining of a suspension of the organisms in a very acid solution of toluidine blue results in only the granules (which possess a very strong affinity for basic dyes) taking up the stain, the remainder of the protoplasm staying colourless.  

  • Levinthal’s medium

    Rabbit or human blood, 5 per cent, added to molten nutrient agar, mixed and heated in boiling water. The supernatant agar after settling is poured as a medium or Haemophilus species.  

  • Levaditi’s stain

    Method for spirochaetes in tissues. The fixed tissue is stained in silver nitrate – pyridine solution, and reduced in formalin – acetone – pyridine, prior to paraffin embedding and section cutting.