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液態培養誘導黑殭菌(Metarhizium anisopliae)產孢研究

The Induction of Submerged Conidiation of Metarhizium anisopliae Study

摘要


本試驗主要目的在於利用氯化鈣(CaCl2)及不同水勢(water potential)來誘導黑殭菌於液態培養環境中產生分生孢子。本試驗分別添加7.3%及24%之polyethylene glycol(PEG 200)於液態培養基malt extract broth(MEB)分別將培養基水勢調整為-2.1Mpa及-7.0Mpa,並分別添加20及40mM氯化鈣(CaCl2),於25°C、150 rpm的環境下培養5天,計算分生孢子之濃度。MEB未添加氯化鈣且未調整水勢者,培養5天之分生孢子濃度為2.39x10^5 conidia/ml;另外,未調整水勢但添加20mM氯化鈣之培養條件下,所產生之分生孢子量最高,約47.6x10^5 conidia/ml。本試驗結果發現,以MEB培養雖可產生分生孢子,但添加氯化鈣之後可明顯增加分生孢子之產量。此外,培養基水勢調整至-7.0Mpa者,無論添加氯化鈣與否,皆無法產生分生孢子。

關鍵字

黑殭菌 氯化鈣 分生孢子 水勢

並列摘要


This study was to determine the induction of submerged conidiation of Metarhizium anisopliae var. anisopliae, using an malt extract broth. Polyethylene glycol (PEG) 200 was added at 7.3% and 24% (w/v) to achieve the water potential (Ψ) of the final broth at -2.1 Mpa and -7.0 Mpa, respectively. Also, calcium chloride (CaCl2) was added at 20 and 40 mM, respectively. Samples of M. anisopliae var. anisopliae incubated at 25°C on a rotary shaker at 150 rpm for 5 days. Conidia yields were at 2.39 × 10^5 conidia/ml in unmodified and non-calcium medium after 5 days. Adding calcium chloride at 20 mM to unmodified MEB increased the production of M. anisopliae conidia to 47.6 × 10^5 conidia/ml. However, no conidia were produced in -7.0 Mpa broth with or without calcium chloride.

被引用紀錄


王淞民(2009)。基轉超寄生菌Trichoderma spp.黑色素生合成基因以提昇其逆境抗性與致病力〔碩士論文,國立臺灣大學〕。華藝線上圖書館。https://doi.org/10.6342/NTU.2009.03041
鐘珮哲(2005)。轉殖蟲生真菌黑色素生合成基因以增加其逆境之抗性〔碩士論文,國立臺灣大學〕。華藝線上圖書館。https://doi.org/10.6342/NTU.2005.00572

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