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"Penelitian bertujuan mengetahui identitas khamir dari saluran pencernaan lebah pekerja pengumpul nektar (nectar collecting bee, NCB) Apis mellifera yang mengunjungi bunga kapuk (Ceiba pentandra) di Jepara. Sebanyak 12 isolat khamir diidentifikasi berdasarkan data sequence daerah Internal Transcribed Spacers (ITS) rDNA. Primer forward ITS1 dan primer reverse ITS4 digunakan untuk amplifikasi daerah ITS rDNA. Hasil elektroforesis produk PCR menunjukkan ukuran daerah ITS rDNA isolat khamir-khamir tersebut bervariasi antara 400 pb hingga 800 pb. Berdasarkan hasil pencarian homologi sequence daerah ITS rDNA m2elalui program Basic Local Alignment Search Tool (BLAST), analisis filogenetik dengan metode Neighbor Joining, dan pengamatan karakter morfologi, 12 isolat khamir tersebut diidentifikasi ke dalam empat genus dan lima spesies. Berdasarkan taksonomi, 11 isolat khamir termasuk ke dalam anggota order Sacharomycetales, class Hemiascomycetes dari phylum Ascomycota dan satu isolat termasuk ke dalam anggota order Ustilaginales, class Ustilaginomycetes dari phylum Basidiomycota. Isolat-isolat tersebut diidentifikasi sebagai Candida parapsilosis (JZ102, JZ105, JZ116, dan JZ121), Candida rugosa (JZ117, JZ121), Debaryomyces hansenii (JZ100, JZ113, JZ118), Meyerozyma caribbica (JZ124, JZ125), dan Pseudozyma sp. (JZ104).

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The aim of this study was to identify the yeast isolates from the digestive tracts of nectar collecting bees (NCB) of Apis mellifera. A total of 12 yeast isolates from the digestive tracts of NCB foraging on flowers of Ceiba pentandra in Jepara, Central Java, were identified based on sequence data of Internal Transcribed Spacers Regions of ribosomal DNA (ITS rDNA). The primer set of ITS1 (forward primer) and ITS4 (reverse primer) were used to amplify the ITS rDNA of the isolates. Gel electrophoresis results showed that the size of ITS region rDNA of the isolates were varied on the range of 400 bp -- 800 bp. Based on sequence homology search results by Basic Local Alignment Search Tool (BLAST) program, phylogenetic analysis by Neighbor Joining method, and morphological characterization, those 12 isolates were identified into four genera and five species. Taxonomically, 11 isolates belong to order Sacharomycetales, class Hemiascomycetes from the phylum Ascomycota and 1 isolate belongs to order Ustilaginales, class Ustilaginomycetes from the phylum Basidiomycota. Those isolates were identified as Candida parapsilosis (JZ102, JZ105, JZ116, and JZ121), Candida rugosa (JZ117, JZ121), Debaryomyces hansenii (JZ100, JZ113, JZ118), Meyerozyma caribbica (JZ124, JZ125), and Pseudozyma sp. (JZ104). "

"Penelitian bertujuan untuk mengetahui identitas khamir dari saluran pencernaan lebah madu Apis mellifera L. yang mengunjungi bunga kapuk (Ceiba pentandra (L.) Gaertn) di Jepara. Sebanyak 12 isolat khamir yang terdiri atas 3 isolat dari saluran pencernaan lebah pejantan (drone) dan 9 isolat dari lebah pekerja pengumpul polen (pollen collecting bees, PCB) diidentifikasi berdasarkan data sequence daerah internal transcribed spacer (ITS) rDNA. Primer yang digunakan untuk amplifikasi daerah ITS adalah primer forward ITS1 atau primer reverse ITS4. Hasil elektroforesis produk PCR menunjukkan daerah ITS rDNA khamirkhamir tersebut bervariasi antara 400 pb hingga 750 pb. Berdasarkan hasil pencarian homologi sequence daerah ITS rDNA melalui program basic local alignment search tool (BLAST), analisis filogenetik dengan metode Neighbor Joining, dan pengamatan karakter morfologi, 12 isolat tersebut diidentifikasi ke dalam empat genus dan tujuh spesies. Berdasarkan taksonomi, khamir-khamir tersebut termasuk kedalam family Candidaceae dan Saccharomycetaceae, order Saccharomycetales, class Hemiascomycetes dari phylum Ascomycota. Isolat-isolat tersebut diidentifikasi ke dalam spesies Candida magnoliae (isolat JZ078), C. orthopsilosis (isolat JZ068 dan JZ069), C. parapsilosis (isolat JZ067 dan JZ095), Debaryomyces hansenii (isolat JZ083 dan JZ096), Meyerozyma caribbica (isolat JZ094), Zygosaccharomyces mellis (isolat JZ075), dan Z. siamensis (isolat JZ054,JZ055, dan JZ056).

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The aim of this research was to determine the identity of the yeasts isolated from the digestive tract of honey bee Apis mellifera that visit flowers of kapok (Ceiba pentandra (L.) Gaertn) in Jepara. A total of 12 yeast isolates consist of 3 isolates from digestive tract of drones and 9 isolates from digestive tract of pollen collecting bees (PCB) were identified based on sequence data of internal transcribed spacers regions of ribosomal DNA (ITS rDNA). The primer set of ITS1 (forward primer) and ITS4 (reverse primer) were used to amplify the ITS rDNA of yeasts. The results of electrophoresis of PCR products showed ITS region rDNA of yeast isolates varied between 400bp--750 bp. Based on sequence homology search results by basic local alignment search tool (BLAST) program, phylogenetic analysis by Neighbor Joining method, and morphological characterization, those 12 isolates were identified into four genera and seven species. Taxonomically, 11 isolates belong to family Candidaceae and Saccharomycetaceae, order Saccharomycetales, class Hemiascomycetes of the phylum Ascomycota. Those isolates were identified as species Candida magnoliae (isolat JZ078), C. orthopsilosis (isolat JZ068 and JZ069), C. parapsilosis (isolat JZ067 and JZ095), Debaryomyces hansenii (isolat JZ083 and JZ096), Meyerozyma caribbica (isolat JZ094), Zygosaccharomyces mellis (isolat JZ075), and Z. siamensis (isolat JZ054, JZ055, and JZ056)."

"Penelitian bertujuan mengetahui identitas khamir dari saluran pencernaan lebah pekerja pengumpul polen (pollen collecting bees, PCB) Apis mellifera. Sebanyak 12 isolat khamir dari saluran pencernaan PCB yang mengunjungi bunga kapuk Ceiba pentandra di Jepara, Jawa Tengah, diidentifikasi berdasarkan data sequence daerah internal transcribed spacer (ITS) rDNA. Amplifikasi daerah ITS rDNA menggunakan primer forward ITS1 dan primer reverse ITS4. Elektroforesis produk PCR menunjukkan bahwa daerah ITS rDNA khamir-khamir tersebut berukuran antara 400--900 pb. Berdasarkan hasil pencarian homologi sequence menggunakan program basic local alignment search tool (BLAST), analisis filogenetik menggunakan metode Neighbor Joining (NJ), dan karakterisasi morfologi, 12 isolat khamir tersebut terdiri dari tujuh spesies yang termasuk dalam lima genus. Secara taksonomi, seluruh khamir tersebut termasuk phylum Ascomycota, class Hemiascomycetes, dan order Saccharomycetales. Isolat-isolat tersebut diidentifikasi sebagai Candida magnoliae (isolat JZ002), Candida orthopsilosis (isolat JZ003, JZ008, JZ011, dan JZ034), Candida rugosa (isolat JZ010); Debaryomyces hansenii (isolat JZ001); Meyerozyma caribbica (isolat JZ013 dan JZ014), Pichia guilliermondii (isolat JZ015), dan Zygosaccharomyces siamensis (isolat JZ005 dan JZ006).

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The aim of this study was to obtain the identity of yeasts from digestive tracts of pollen collecting bees (PCB) Apis mellifera. A total of 12 yeast isolates obtained from digestive tract of PCB foraging on flowers Ceiba pentandra in Jepara, Central Java, were identified based on sequence data of internal transcribed spacer of ribosomal DNA (ITS rDNA). The primer set of ITS1 (forward primer) and ITS4 (reverse primer) were used to amplify the ITS region rDNA. Gel electrophoresis result showed that the size of ITS rDNA of those yeast were varied between 400--900 base pairs. Based on sequence homology search using basic local alignment search tool (BLAST) program, phylogenetic analysis by Neighbor Joining method, and morphological characterization, those 12 isolates belong to five genera and seven species. Taxonomically, all of those isolates belong to order Saccharomycetales, class Hemiascomycetes from the phylum Ascomycota. Those 12 isolates were identified as species Candida magnoliae (isolate JZ002); Candida orthopsilosis (isolates JZ003, JZ008, JZ011, and JZ034); Candida rugosa (isolate JZ010); Debaryomyces hansenii (isolate JZ001); Meyerozyma caribbica (isolates JZ013 and JZ014); Pichia guilliermondii (isolate JZ015); and Zygosaccharomyces siamensis (isolates JZ005 and JZ006)."

"Penelitian bertujuan untuk mengetahui identitas khamir yang hidup pada putik bunga Ceiba pentandra (L.) Gaertn dan saluran pencernaan Apis mellifera L., lebah pengumpul polen yang mengunjungi bunga Ceiba pentandra. Sebanyak 12 isolat khamir yang terdiri dari tiga isolat dari putik bunga Ceiba pentandra dan sembilan isolat dari saluran pencernaan Apis mellifera digunakan pada penelitian. Isolat-isolat khamir diidentifikasi berdasarkan hasil Basic Local Alignment Searching Tools (BLAST) data sequence daerah ITS rDNA, analisis filogenetik dengan metode Neighbor Joining, dan pengamatan alat reproduksi seksual dan aseksual. Primer forward ITS1 dan primer reverse ITS4 digunakan untuk mengamplifikasi daerah ITS rDNA. Hasil elektroforesis gel produk PCR menunjukkan ukuran daerah ITS rDNA isolat khamir tersebut bervariasi antara 400 hingga 800 pb. Hasil menunjukkan bahwa 12 isolat khamir terdiri dari enam species. Lima species khamir termasuk ke dalam phylum Ascomycota, order Saccharomycetales, class Saccharomycetes dan satu species khamir termasuk ke dalam phylum Basidiomycota, order Tremellales,dan class Tremellomycetes. Tiga isolat khamir dari putik bunga C. pentandra diidentifikasi sebagai Bullera coprosmaensis (JZ137), Candida orthopsilosis (JZ053), dan Debaryomyces hansenii (JZ051). Sembilan isolat khamir dari saluran pencernaan A. mellifera diidentifikasi sebagai Candida fermentatii (JZ059 dan JZ060), Candida mesorugosa (JZ057, JZ058, dan JZ063), Candida orthopsilosis (JZ064 dan JZ065), Candida parapsilosis (JZ066), dan Debaryomyces hansenii (JZ061). Dua species khamir yaitu Candida orthopsilosis dan Debaryomces hansenii ditemukan pada putik C. pentandra dan saluran pencernaan A. mellifera.

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The aim of this study was to identify yeasts from the pistils of Ceiba pentandra (L.) Gaertn and digestive tracts of pollen collecting bee, Apis mellifera L. Twelve yeast isolates were identified which were consisted of three isolates from the pistils of C. pentandra and nine isolates from digestive tracts of A. mellifera. Identification was based on homology sequences analysis using Basic Local Alignment Searching Tools (BLAST), phylogenetic analysis by Neighbor Joining method, and observation of sexual and asexual reproduction. The primer set of ITS1 (forward primer) and ITS4 (reverse primer) were used to amplify ITS region rDNA of the isolates. Gel electrophoresis results showed that the size of ITS region of the isolates were varied on the range of 400--800 bp.

The results showed that twelve yeast isolates were identified as six species. Taxonomically, five species belong to phylum Ascomycota, order Saccharomycetales, class Saccharomycetes and one species belong to phylum Basidiomycota order Tremellales, class Tremellomycetes. Three yeast isolates from the pistils of C. pentandra were identified as Bullera coprosmaensis (JZ137), Candida orthopsilosis (JZ053), and Debaryomyces hansenii (JZ051). Nine yeast isolates from digestive tracts of pollen collecting A. mellifera were identified as Candida fermentatii (JZ059 & JZ060), Candida mesorugosa (JZ057, JZ058, dan JZ063), Candida orthopsilosis (JZ064 & JZ065), Candida parapsilosis (JZ066), and Debaryomyces hansenii (JZ061). Debaryomyces hansenii and Candida orthopsilosis were found on the pistils of C. pentandra and digestive tracts of A. mellifera."

"Penelitian bertujuan mengetahui keragaman spesies khamir dari saluran pencernaan lebah madu Apis cerana di apiari Desa Ciburial, Bandung. Sebanyak 48 isolat khamir dari saluran pencernaan Pollen-collecting bee (PCB) (27 isolat) dan Nectarcollecting bee (NCB) (21 isolat) diidentifikasi berdasarkan data sequence daerah internal transcribed spacer (ITS) rDNA dan dikarakterisasi secara morfologi untuk melengkapi hasil identifikasi. Hasil identifikasi molekuler menunjukkan bahwa 48 isolat khamir tersebut terdiri atas delapan genus dan 16 spesies. Sebanyak 12 spesies khamir ditemukan pada PCB dan sembilan spesies khamir ditemukan pada NCB. Candida cf. apicola, C. etchellsii, Debaryomyces hansenii, Rhodotorula mucilaginosa dan Zygosaccharomyces rouxii ditemukan pada PCB maupun NCB. Spesies-spesies khamir yang diperoleh secara taksonomi heterogen, yaitu termasuk ke dalam class Hemiascomycetes dari phylum Ascomycota (13 spesies) dan class Urediniomycetes dari phylum Basidiomycota (3 spesies).

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The aim of this study was to study the diversity of yeast species isolated from the digestive tract of honey bee Apis cerana in apiary in Ciburial, Bandung. A total of 48 yeast isolates from the digestive tract of pollen-collecting bees (27 isolates) and Nectar-collecting bee (21 isolates) were identified based on sequence data of internal transcribed spacers regions of ribosomal DNA (ITS rDNA). In addition of their sequence data, yeasts were also characterized morphologically. The results showed that those yeasts comprised of eight genera and 16 species. Twelve yeast species were found from PCB and nine yeast species were found from NCB. Candida cf. apicola, C. cf. azyma, C. etchellsii, C. naeodendra, C. orthopsilosis, Cryptococcus heveanensis, Debaryomyces hansenii, Rhodotorula mucilaginosa and Zygosaccharomyces rouxii were found both in PCB and NCB. Our molecular analysis showed that A. cerana harbors taxonomically diverse yeasts. They consisted of species belong to the class Hemiascomycetes of the phylum Ascomycota (13 species) and class Urediniomycetes of the phylum Basidiomycota (3 species)."

"Penelitian ini bertujuan untuk mengidentifikasi 16 strain kapang dari tujuh manuskrip kuno berbahan kertas Eropa dengan analisis sekuens daerah internal transcribed spacers (ITS) pada rDNA dan melakukan deskripsi morfologi terhadap kapang-kapang tersebut. Kapang tersebut berasal dari manuskrip kuno asal Keraton Kasepuhan Cirebon dan Perpustakaan Fakultas Ilmu Pengetahuan Budaya Universitas Indonesia (FIB UI). Amplifikasi daerah ITS rDNA menggunakan forward primer ITS 1 dan reverse primer ITS 4. Deskripsi morfologi dilakukan pada medium Czapek’s Dox Agar (CDA). Panjang fragmen daerah ITS berdasarkan elektroforesis gel dari kapang genus Aspergillus adalah 500--800 pb, Penicillium 500--600 pb, dan mycelia sterilia 550--800 pb. Satu strain kapang merupakan anggota filum Ascomycota, kelas Loculoascomycetes,ordo Dothideales, famili Davidielaceae, dan memiliki homologi sekuens daerah ITS dengan spesies terdekatnya, yaitu Cladosporium cladosporioides (Fresen.). Sebanyak 13 strain merupakan anggota filum Ascomycota, kelas Plectomycetes,ordo Eurotiales, famili Trichocomaceae, dan memiliki homologi sekuens daerah ITS dengan spesies terdekatnya, yaitu Aspergillus flavus Link. (satu strain),Aspergillus oryzae Cohn. (dua strain), Aspergillus niger (dua strain), Penicillium citrinum Thom (empat strain), Penicillium griseofulvum Dreckx. (satu strain),Penicillium janthinellum Biourd (satu strain), Eurotium amstelodami L. Mangin (satu strain), dan Eurotium rubrum Jos. Konig. (satu strain). Dua strain kapang lainnya, yaitu satu strain Aspergillus sp. dan satu strain Penicillium sp. belum berhasil diidentifikasi hingga tingkat spesies.

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The aim of this research was to identify 16 strains of moulds from seven old European paper manuscripts based on sequence analysis of ITS region rDNA and to describe their morphology. The moulds were isolated from old manuscripts from Keraton Kasepuhan Cirebon and the library of Faculty of Humanities University of Indonesia. ITS 1 and ITS 4 primers were used as forward and reverse primers for PCR, respectively. The mould’s morphology was examined on Czapek’s Dox Agar (CDA). The lengths of ITS region of genus Aspergillus based on gel electrophoresis were on the range of 500--800 bp, Penicillium 500--600 bp, and mycelia sterilia 550--800 bp. One strain belongs to phylum Ascomycota, class Loculoascomycetes, order Dothideales, family Davidielaceae,and showed ITS region similarity to Cladosporium cladosporioides (Fresen.).

Thirteen strains belong to phylum Ascomycota, class Plectomycetes, order Eurotiales, family Trichocomaceae, and showed ITS region similarities to Aspergillus flavus Link. (one strain), Aspergillus oryzae Cohn. (two strains),Aspergillus niger (two strains), Penicillium citrinum Thom (four strains),Penicillium griseofulvum Dreckx. (one strain), Penicillium janthinellum Biourd (one strain), Eurotium amstelodami L. Mangin (one strain), and Eurotium rubrum Jos. Konig. (one strain). One strain of Aspergillus sp. and one strain of Penicillium sp. were unable to be identified to species level."

"Penelitian ini bertujuan untuk mengidentifikasi 15 strain kapang dari lima manuskrip kuno berbahan kertas daluang asal perpustakaan Fakultas Ilmu Pengetahuan Budaya Universitas Indonesia (FIB UI) dan melakukan deskripsi morfologi kapang-kapang tersebut. Identifikasi dilakukan berdasarkan analisis sekuens daerah Internal Transcribed Spacers (ITS) rDNA dan pengamatan morfologi kapang dilakukan pada Czapek’s Dox Agar (CDA). Primer forward ITS1 dan primer reverse ITS4 digunakan untuk amplifikasi daerah ITS rDNA.Hasil elektroforesis produk PCR menunjukkan panjang daerah ITS dari 15 strain kapang tersebut bervariasi antara 500 pb--900 pb. Sebelas strain kapang memiliki homologi ITS rDNA dengan spesies terdekat Aspergillus clavatus Desm. (1 strain), Aspergillus flavus group (1 strain), Aspergillus niger van Tieghem (1 strain), Penicillium citrinum Thom (6 strain), Penicillium janthinellum Biourge (1 strain), dan Penicillium oxalicum Currie & Thom (1 strain) dan termasuk anggota ordo Eurotiales, kelas Plectomycetes, dari filum Ascomycota. Satu strain memiliki homologi ITS rDNA dengan spesies terdekat Pseudocercospora sp. (1 strain) dan termasuk anggota ordo Capnodiales, kelas Dotthideomycetes, dari filum Ascomycota. Tiga strain kapang (Penicillium sp. FIB.PRI.6.1, Fraseriella sp. FIB.PRI.6.2, dan mycelia sterilia FIB.PRII.3) belum berhasil diidentifikasi hingga tingkat spesies.

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The aims of this research were to identify 15 mould strains from five old manuscripts of daluang paper from the library of Fakultas Ilmu Pengetahuan Budaya Universitas Indonesia (FIB UI) and to describe their morphology. Identification was carried out based on analysis of Internal Transcribed Spacers (ITS) region of rDNA sequence. Observation of the mould’s morphology was carried out on Czapek’s Dox Agar (CDA). Forward primer ITS1 and reverse primer ITS4 were used to amplify the ITS region of rDNA. Gel electrophoresis results showed that the lengths of ITS region from 15 mould strains were on the range of 500 bp--900 bp.

Eleven strains showed ITS rDNA sequence similarities to Aspergillus clavatus Desm. (1 strain), Aspergillus flavus group (1 strain), Aspergillus niger van Tieghem (1 strain), Penicillium citrinum Thom (6 strains), Penicillium janthinellum Biourge (1 strain), Penicillium oxalicum Currie & Thom (1 strain). The strains belong to order Eurotiales, Class Plectomycetes, phylum Ascomycota. One strain showed ITS rDNA sequence similarity to Pseudocercospora sp. (1 strain). The strain belongs to order Capnodiales, class Dotthideomycetes, phylum Ascomycota. Three strains (Penicillium sp. FIB.PRI.6.1, Fraseriella sp. FIB.PRI.6.2, and mycelia sterilia FIB.PRII.3) were unable to be identified to species level."

"Penelitian bertujuan untuk mengetahui pengaruh pemberian pollen substitute (PS) mengandung biomassa C. hawaiiana CR014 terhadap jumlah larva dan pupa lebah pekerja A. mellifera. Sebagai kontrol positif koloni lebah madu diberi pakan tambahan pollen jagung. Pemberian pakan dilakukan sekali seminggu selama enam minggu pada musim kemarau. Hasil uji ANOVA satu faktor menunjukkan bahwa rerata jumlah larva yang dihasilkan per minggu pada koloni perlakuan dan koloni kontrol positif tidak berbeda nyata (P>0,05). Begitu pula dengan rerata jumlah pupa pada koloni perlakuan dan kontrol positif per minggu tidak berbeda nyata (P>0,05). Hasil uji T juga menunjukkan bahwa rerata jumlah larva dan pupa per minggu antara koloni perlakuan dan koloni kontrol positif tidak berbeda nyata (P>0,05). Pemberian PS pada A. mellifera memberikan pengaruh yang hampir sama baiknya dengan pemberian pollen jagung terhadap jumlah larva dan pupa lebah pekerja A. mellifera selama periode pengamatan tujuh minggu. Hasil penelitian memperlihatkan bahwa PS yang mengandung biomassa C. hawaiiana CR014 dapat menggantikan peran pollen alami sebagai sumber protein A. mellifera untuk mempertahankan produktivitas koloninya pada musim kemarau.

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The research aimed to examine the effect of pollen substitute (PS) containing Candida hawaiiana CR014 on the number of larvae and pupae of worker bees Apis mellifera. Colonies of a positive control were fed with maize?s pollen. The colonies were fed once a week for six weeks in the dry season. The one-way Anova test showed that the mean number of larvae produced per week in the treated group were not significantly difference from the positive control (P> 0,05). Similarly, the mean number of pupae produced per week in treated group and the positive control were not significantly difference (P>0,05).

The T-test showed that the mean number of larvae and pupae per week between the treated group and the positive control were not significantly difference (P>0,05). The study indicated that PS and the maize?s pollen has an almost similar effect on the number of larvae and the number of pupae of worker bees produced by the colonies during the experiment. It is concluded that PS containing C. hawaiiana CR014 might be used to replace natural pollens as a protein source to maintain productivity of A. mellifera during the dry season."

" ABSTRAK Penelitian ini bertujuan untuk memperoleh identitas spesies kapang dari dua manuskrip Cina lama yang mengalami deteriorasi asal plot 5 Ruang Naskah Perpustakaan Pusat Universitas Indonesia PP-UI , Depok berdasarkan data sekuens daerah internal transcribed spacers ribosomal DNA ITS rDNA . Pengambilan sampel pada manuskrip menggunakan metode swab dengan cotton bud steril. Isolasi kapang menggunakan metode culture-dependent. Polymerase chain reaction PCR dan DNA sequencing menggunakan primer forward ITS5 dan primer reverse ITS4. Pencarian homologi sekuens daerah ITS rDNA menggunakan program basic local alignment search tool BLAST dan pembuatan pohon filogenetik menggunakan metode Neighbor Joining, model dua parameter Kimura, serta bootstrap sebanyak 1.000 kali replikasi. Penentuan spesies terdekat dan posisi taksonomi menggunakan analisis filogenetik dan didukung oleh data morfologi. Isolasi kapang menghasilkan enam isolat kapang terpilih berdasarkan tipe morfologi yang berbeda dengan kapang dari manuskrip Cina lama asal plot 1, 2, 4, dan 6 Ruang Naskah PP-UI, Depok. Berdasarkan elektroforesis gel, panjang fragmen daerah ITS rDNA dari enam isolat kapang bervariasi antara 600--700 pb. Hasil DNA sequencing lengkap menunjukkan panjang daerah ITS rDNA enam isolat berkisar 582--625 pb. Enam strain UICC merupakan anggota dari tiga kelas Dothideomycetes, Eurotiomycetes dan Sordariomycetes , tiga ordo Capnodiales, Eurotiales dan Hypocreales , dan empat famili Cladosporiaceae, Nectriaceae, Ophiocordycipitaceae, dan Pleosporaceae . Strain UICC 1107 memiliki homologi 99,32 dengan type strain Purpureocillium lilacinum sin. Paecilomyces lilacinus ATCC 10114T. Lima strain UICC tidak dapat ditentukan spesiesnya. Strain UICC 1106 adalah Cladosporium sp. dengan homologi 100 terhadap type strain Cladosporium oxysporum CBS 125991T dan Cla. tenuissimum CPC 14235T. Strain UICC 1105 adalah Curvularia sp.1 dengan homologi 93,80 dan strain UICC 1108 adalah Curvularia sp.2 dengan homologi 94,70 terhadap type strain Curvularia carica-papayae CBS 135941T. Strain UICC 1109 adalah Rectifusarium sp. dengan homologi 85,87 terhadap type strain Rectifusarium robinianum CBS 430.91T. Strain UICC 1104 adalah Sarocladium sp. dengan homologi 97,13 terhadap type strain Sarocladium bifurcatum UTHSC 05-3311T. Enam strain UICC merupakan fungi anamorf dan bersifat xerofilik.

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ABSTRACT The aim of this study was to determine the species identity of moulds from two deteriorated old Chinese manuscripts from plot 5 Ruang Naskah Central Library Universitas Indonesia, Depok based on internal transcribed spacers region of ribosomal DNA ITS rDNA . Samples from the manuscripts were collected by using swab method with sterile cotton swabs. Mould isolates were obtained by culture dependent method. Polymerase chain reaction PCR and DNA sequencing were performed using forward primer ITS5 and reverse primer ITS4. Homology search of ITS rDNA sequences was carried out using basic local alignment search tool BLAST program and phylogenetic tree construction was performed using Neighbor Joining method, Kimura rsquo s two parameter model, and bootstrap 1,000 replicates. The closest species and taxonomic position were obtained by phylogenetic analysis and supported by morphological data. Six mould isolates were selected based on morphological type differences compared to mould isolates from old Chinese manuscripts from plot 1, 2, 4, and 6 Ruang Naskah Central Library UI, Depok. Based on gel electrophoresis, the lengths of ITS rDNA fragments of six mould isolates varied between 600 700 bp. Full sequence data of ITS rDNA of six isolates showed that the lengths of their ITS rDNA varied between 582 625 bp. Six UICC strains belonged to three classes Dothideomycetes, Eurotiomycetes and Sordariomycetes , three orders Capnodiales, Eurotiales and Hypocreales , and four families Cladosporiaceae, Nectriaceae, Ophiocordycipitaceae, and Pleosporaceae . UICC 1107 strain showed 99.32 homology to the type strain, Purpureocillium lilacinum syn. Paecilomyces lilacinus ATCC 10114T. Five UICC strains were not able to be determined to the species level. UICC 1106 strain was identified as Cladosporium sp., with 100 homology to the type strains, Cladosporium oxysporum CBS 125991T and Cla. tenuissimum CPC 14235T. UICC 1105 strain was identified as Curvularia sp.1, with 93.80 homology and UICC 1108 strain was identified as Curvularia sp.2, with 94.70 homology to the type strain, Curvularia carica papayae CBS 135941T. Strain UICC 1109 was identified as Rectifusarium sp., with 85.87 homology to the type strain, Rectifusarium robinianum CBS 430.91T. Strain UICC 1104 was identified as Sarocladium sp., with 97.13 homology to the type strain, Sarocladium bifurcatum UTHSC 05 3311T. Six UICC strains were anamorphic and xerophilic fungi."