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"Metarhizium majus UICC 295 adalah kapang entomopatogen. Penelitian bertujuan mengetahui pengaruh penambahan tepung jangkrik 10% (b/v) pada medium pertumbuhan M. majus UICC 295 terhadap kemampuan menginfeksi larva O. rhinoceros serta mengetahui pengaruh preservasi pada suhu -80o C menggunakan protektan gliserol 10% (v/v) dan gliserol 10% (v/v) dengan trehalosa 5% (b/v) terhadap viabilitas M. majus UICC 295. Konidia/hifa dari Saboraud Dextrose with Yeast Extract Agar (SDYA) dengan penambahan tepung jangkrik 10% (b/v) mampu membunuh larva 6,6--100% dalam 8--11 hari. Konidia/hifa yang dipreservasi selama 30 hari pada suhu -80o C menggunakan gliserol 10% (v/v) dan gliserol 10% (v/v) + trehalosa 5% (b/v) mengalami penurunan viabilitas. Konidia/hifa yang dipreservasi bersama kadaver larva selama 30 hari pada suhu -80o C menggunakan gliserol 10% (v/v) dan gliserol 10% (v/v) dengan trehalosa 5% (b/v) mampu dipertahankan viabilitasnya.

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Metarhizium majus UICC 295 is an entomopathogenic fungus. This research aimed to investigate the effect of 10% (w/v) cricket powder in growth medium on the pathogenicity of M. majus UICC 295 to infect O. rhinoceros larvae and to investigate the effect of freezing in -80o C using 10% (v/v) glycerol and 10% (v/v) glycerol with 5% (w/v) trehalose on its viability. The conidia/hyphae from Saboraud Dextrose Agar with Yeast Extract (SDAY) with 10% (w/v) cricket powder was able to kill larvae 6.6%--100% in 8--11 days. Viability of conidia/hyphae after being preserved for 30 days in -80o C with 10% (v/v) glycerol and 10% (v/v) glycerol with 5% (w/v) trehalose was decreased. The conidia/hyphae on cadaver was still viable after being preserved at -80o C with 10% (v/v) glycerol and 10% (v/v) glycerol with 5% (w/v) trehalose."

"Penelitian ini bertujuan untuk memperoleh informasi mengenai pengaruh variasi mediumpertumbuhan terhadap pembentukan miselium aerial dan aktivitas antimikroba delapanisolat rare Actinobacteria termofilik dari tanah di sekitar geiser Cisolok, Jawa Barat.Pengujian pertumbuhan, pembentukan miselium aerial, dan aktivitas antimikrobadilakukan dengan menumbuhkan isolat pada medium ISP 1 agar, ISP 1 gellan gum, ISP2 agar, ISP 2 gellan gum, ISP 3 agar, ISP 3 gellan gum, Bennett’s agar, Bennett’s gellangum, Minimal (Mm) 3 agar, Mm 3 gellan gum, 2% agar, dan 2% gellan gum. Isolatkemudian diinkubasi pada suhu 45 °C selama 7 dan 14 hari. Konfirmasi suhupertumbuhan menunjukkan 2 isolat dapat tumbuh hingga suhu 45 °C dan 6 isolat dapattumbuh hingga 50 °C. Hasil pengujian variasi medium pertumbuhan menunjukkan semuaisolat rare Actinobacteria dapat menghasilkan miselium substrat pada semua medium.Hasil pengamatan setelah inkubasi selama 7 hari pada suhu inkubasi 45 °C menunjukkanisolat-isolat tersebut dapat menghasilkan miselium aerial pada medium ISP 1 agar (2isolat), Mm 3 agar (3 isolat), 2% agar (5 isolat), dan 2% gellan gum (5 isolat). Hasilpengamatan setelah inkubasi selama 14 hari menunjukkan isolat-isolat tersebut dapatmenghasilkan miselium aerial pada medium ISP 1 gellan gum (2 isolat), ISP 2 agar (1isolat), ISP 2 gellan gum (3 isolat), ISP 3 agar dan gellan gum (2 isolat), Mm 3 agar 3isolat, dan Mm 3 gellan gum (3 isolat). Hasil pengujian aktivitas antibakteri menunjukkanisolat SL3-2-R-11 yang ditumbuhkan pada medium ISP 3 gellan gum dan SL3-1-R-7yang ditumbuhkan pada Bennett’s agar selama 7 hari dapat menghambat pertumbuhanStaphylococcus aureus. Hasil pengujian aktivitas antikhamir menunjukkan isolat SL3-2-R-11 yang ditumbuhkan pada medium ISP 3 gellan gum dan SL3-1-R-7 pada mediumBennett’s agar selama 14 hari dapat menghambat pertumbuhan Candida albicans. Hasilpengujian aktivitas antifungi menunjukkan tidak ada isolat yang dapat menghambatpertumbuhan Aspergillus flavus.

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This study aims to obtain information about the effect of growth medium variations onthe formation of aerial mycelium and antimicrobial activity of eight thermophilic rareActinobacteria isolates from the soil around Cisolok geyser, West Java. The ability togrow at various media, aerial mycelium formation, and antimicrobial activity were carriedout by growing isolates on medium ISP 1 agar, ISP 1 gellan gum, ISP 2 agar, ISP 2 gellangum, ISP 3 agar, ISP 3 gellan gum, Bennett’s agar, Bennett’s gellan gum, Minimum (Mm)3 agar, Mm 3 gellan gum, 2% agar, and 2% gellan gum. The isolates were then incubatedat 45 oC for 7 and 14 days. Growth test at various temperatures showed that two isolatescould grow at a temperature of 45 oC and six isolates could grow up to 50 oC. The resultsof the growth medium variation test showed that all rare Actinobacteria isolates couldproduce substrate mycelium in all mediums. Observations after incubation for 7 days at45 °C showed that these isolates could produce aerial mycelium on ISP 1 agar medium(2 isolates), Mm 3 agar (3 isolates), 2% agar (5 isolates), and 2% gellan gum (5 isolates).Observations after incubation for 14 days showed that these isolates could produce aerialmycelium on the medium ISP 1 gellan gum (2 isolates), ISP 2 agar (1 isolate), ISP 2gellan gum (3 isolates), ISP 3 agar and gellan gum (2 isolates), Mm 3 agar 3 isolates, andMm 3 gellan gum (3 isolates). The results of antibacterial activity test showed that isolatesSL3-2-R-11 grown on ISP 3 gellan gum and SL3-1-R-7 grown on Bennett’s agar for 7days could inhibit the growth of Staphylococcus aureus. The antifungal activity test ofisolates SL3-2-R-11 grown on ISP 3 gellan gum medium and SL3-1-R-7 on Bennett’sagar for 14 days showed inhibition towards Candida albicans. Meanwhile, all isolates didnot show antifungal activity against Aspergillus flavus"