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- Abstract 文献概要
新しい多項目微量検査システム,API 20C®(Analytab Products社製,臨床酵母システム)と酵母同定のためのアメリカ合衆国CDC標準操作法を比較検討した.臨床材料から分離した酵母の44菌株について発酵と利用により検査した.6種類の発酵糖類と10種類の利用糖類について比較した.APIの結果は24時間と48時間培養後に判定し,他方標準CDCシステムでは48時間後に読み,更に必要な場合14日後に判定した.
A new, multitest *2, microtechnique *3 system, API 20 C® (Analytab Products Inc. *4 Clinical Yeast System), was evaluated by comparing it *5 to the U. S. Center for Disease Control (CDC) *6 standard techniques for the identification of yeast *7. Forty-four yeast strains isolated from clinical specimens were tested by fermentation *8 and assimilation *9. Six fermentation carbohydrates and ten assimilation carbohydrates were compared. API results were read *10 after incubation of 24 and 48 hours while the standard CDC system was read after 48 hours and 14 days when needed.
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