MATERIALS AND METHODSGrowth and maintenance of micro-organismsThe foll translation - MATERIALS AND METHODSGrowth and maintenance of micro-organismsThe foll Indonesian how to say

MATERIALS AND METHODSGrowth and mai

MATERIALS AND METHODS
Growth and maintenance of micro-organisms
The following species were used in the experiments: Staphylococcus epidermidis
(laboratory typed strain isolated from human skin), Candida albicans NCTC 10288
and Fusobacterium nucleatum (subspecies nucleatum) ATCC 10953, all obtained
from laboratory stocks. S. epidermidis was maintained on Nutrient Agar (Oxoid Ltd,
Basingstoke, UK), C. albicans on Potato Dextrose Agar (Oxoid Ltd, Basingstoke,
UK) and F. nucleatum on Fastidious Anaerobe Agar (Oxoid Ltd, Basingstoke, UK)
supplemented with 5% defibrinated horse blood (TCS Biosciences, Buckingham,
UK). Broth cultures of S. epidermidis and C. albicans were grown in 1% tryptone-
0.5% yeast extract and F. nucleatum, in brain-heart infusion broth. S. epidermidis and
C. albicans were incubated at 37ºC aerobically (Genlab M1005L incubator, Cheshire,
UK), and F. nucleatum was incubated at 37ºC anaerobically (MK3 Anaerobic work
station, Don Whitley Scientific, Shipley, UK). All cultures were sub-cultured weekly.
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MATERIALS AND METHODSGrowth and maintenance of micro-organismsThe following species were used in the experiments: Staphylococcus epidermidis(laboratory typed strain isolated from human skin), Candida albicans NCTC 10288and Fusobacterium nucleatum (subspecies nucleatum) ATCC 10953, all obtainedfrom laboratory stocks. S. epidermidis was maintained on Nutrient Agar (Oxoid Ltd,Basingstoke, UK), C. albicans on Potato Dextrose Agar (Oxoid Ltd, Basingstoke,UK) and F. nucleatum on Fastidious Anaerobe Agar (Oxoid Ltd, Basingstoke, UK)supplemented with 5% defibrinated horse blood (TCS Biosciences, Buckingham,UK). Broth cultures of S. epidermidis and C. albicans were grown in 1% tryptone-0.5% yeast extract and F. nucleatum, in brain-heart infusion broth. S. epidermidis andC. albicans were incubated at 37ºC aerobically (Genlab M1005L incubator, Cheshire,UK), and F. nucleatum was incubated at 37ºC anaerobically (MK3 Anaerobic workstation, Don Whitley Scientific, Shipley, UK). All cultures were sub-cultured weekly.
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BAHAN DAN METODE
Pertumbuhan dan pemeliharaan mikro-organisme
Spesies berikut digunakan dalam percobaan: Staphylococcus epidermidis
(laboratorium diketik regangan terisolasi dari kulit manusia), Candida albicans NCTC 10288
dan Fusobacterium nucleatum (subspesies nucleatum) ATCC 10953, semua diperoleh
dari saham laboratorium . S. epidermidis dipertahankan pada Nutrient Agar (Oxoid Ltd,
Basingstoke, UK), C. albicans pada Potato Dextrose Agar (Oxoid Ltd, Basingstoke,
Inggris) dan F. nucleatum pada rewel anaerob Agar (Oxoid Ltd, Basingstoke, UK)
dilengkapi dengan 5% darah kuda defibrinated (TCS Biosciences, Buckingham,
UK). Budaya kaldu dari S. epidermidis dan C. albicans ditumbuhkan dalam 1% tryptone-
0,5% ekstrak ragi dan F. nucleatum, di otak-hati infus kaldu. S. epidermidis dan
C. albicans diinkubasi pada 37ºC aerob (Genlab M1005L inkubator, Cheshire,
UK), dan F. nucleatum diinkubasi pada 37ºC anaerob (pekerjaan MK3 anaerobik
stasiun, Don Whitley Ilmiah, Shipley, UK). Semua budaya yang mingguan sub-kultur.
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