Hasil Pencarian  ::  Simpan CSV :: Kembali

"Penelitian bertujuan untuk memperoleh informasi keanekaragaman khamir daribunga Jatropha integerrima Jacq. di kampus Universitas Indonesia, Depok.Khamir diisolasi dari 30 bunga (15 bunga jantan dan 15 bunga betina). Hasilelektroforesis menunjukkan terdapat polimorfisme panjang (300--700 pb) daerahITS rDNA 26 isolat khamir representatif yang mengindikasikan adanyakeragaman genetik di antara isolat tersebut. Berdasarkan data sequence, 26 isolatkhamir representatif tersebut secara taksonomi beragam, yaitu terdiri dari 13species yang berasal dari phylum Ascomycota (class Hemiascomycetes(Candida)) dan dari phylum Basidiomycota (class Urediniomycetes(Sporidiobolus), Ustilaginomycetes (Pseudozyma & Ustilago), danHymenomycetes (Bullera & Cryptococcus))."

"Pada penelitian sebelumnya, diperoleh 18 strain Candida spp. dari Apis cerana dan bunga-bunga yang dikunjunginya di Ciburial, Jawa Barat. Hasil identifikasi berdasarkan data sequence daerah ITS rDNA menggunakan primer reverse ITS4, menunjukkan bahwa 18 strain tersebut memiliki homologi rendah (85--98%) terhadap spesies terdekatnya Candida spp. Dengan demikian belum diperoleh identitas yang akurat dari 18 strain Candida spp. tersebut. Penelitian bertujuan untuk memperoleh identitas yang akurat dari 18 strain tersebut melalui identifikasi molekuler, analisis filogenetik, dan pengamatan karakter fenotipik (morfologi, fisiologi, dan biokimia). Identifikasi dilakukan melalui sequencing pada daerah ITS rDNA dan D1/D2 LSU rDNA. Analisis filogenetik dilakukan berdasarkan data sequence daerah ITS rDNA dan D1/D2 LSU rDNA, menggunakan metode neighbor-joining. Berdasarkan hasil identifikasi molekuler, analisis filogenetik, dan pengamatan karakter fenotipik, 10 strain diidentifikasi ke dalam 5 spesies, yaitu C. parapsilosis (Candida sp. CR033, CR034, dan CR038), C. orthopsilosis (Candida sp. CR015 dan CR151), C. metapsilosis (Candida sp. CR047 dan CR053), Debaryomyces hansenii (Candida sp. CR065), dan Wickerhamomyces anomalus (Candida sp. CR070 dan CR105). Sebanyak 8 strain (Candida sp. CR004, CR007, CR013, CR014, CR018, CR023, CR027, dan CR035) belum dapat ditentukan nama penunjuk (epithet) spesiesnya. Berdasarkan sequence ITS rDNA 8 strain tersebut memiliki homologi yang rendah (97%) terhadap kerabat terdekatnya C. hawaiiana. Pohon filogenetik berdasarkan sequence ITS rDNA menunjukkan 8 strain tersebut berada pada clade yang terpisah dengan C. hawaiiana dengan dukungan nilai bootstrap yang sangat tinggi, 99%. Delapan strain Candida tersebut termasuk dalam satu spesies yang memiliki perbedaan sequence ≤1% antara satu strain Candida dengan strain Candida lainnya atau disebut conspecific. Karakter fisiologi dan biokimia menunjukkan 8 strain tersebut memiliki perbedaan dengan C. hawaiiana CBS 9146T pada kemampuannya mengasimilasi sumber karbon α- methyl -D-glucoside, dan ketidakmampuannya mengasimilasi ribosa. Hasil identifikasi penelitian menunjukkan bahwa 8 strain Candida tersebut merupakan spesies yang berbeda dengan C. hawaiiana.

---

In the previous study, 18 strains of Candida spp. were obtained from Apis cerana and their visiting flowers in Ciburial, West Java. Based on sequence data of ITS rDNA using ITS4 reverse primer, these strains showed low homology (85--98%) to their closest relatives Candida spp. Therefore, the identity of these 18 strains were not established yet.

The purpose of this study was to establish the identities of the 18 strains of Candida spp. by conducting molecular identification, phylogenetic analysis, and phenotypic characterization (morphological, physiological, and biochemical characters). Identification and phylogenetic analysis was carried out by sequencing the ITS rDNA and D1/D2 of LSU rDNA. Phylogenetic tree was constructed using neighbor-joining method.

Based on molecular identification, phylogenetic analysis, and phenotypic characterization, 10 strains were identified into 5 species. Those 10 strains were identified as C. parapsilosis (Candida sp. CR033, CR034, and CR038), C. orthopsilosis (Candida sp. CR015 and CR151), C. metapsilosis (Candida sp. CR047 and CR053), Debaryomyces hansenii (Candida sp. CR065), and Wickerhamomyces anomalus (Candida sp. CR070 and CR105). The identities of eight strains (Candida sp. CR004, CR007, CR013, CR014, CR018, CR023, CR027, and CR035) were not established yet. Based on sequence data of ITS rDNA they have low degree of homology (97%) to their closest related species, C. hawaiiana.

Phylogenetic tree based on sequence data of ITS rDNA showed they were separated from C. hawaiiana by 99% bootstrap value. Multiple alignment of their sequences of ITS and D1/D2 showed that they have ≤1% differences, which indicate that these strains are conspecific (same species). Their morphological, physiological and biochemical characteristics showed that these strains differed from C. hawaiiana CBS 9146T by their ability to assimilate α-methyl-D-glucoside and their inability to assimilate ribose as carbon sources. Our data suggest that these strains were distinct species from C. hawaiiana."

"Universitas Indonesia Culture Collection (UICC) memiliki koleksi strain-strain Rhizopus oryzae Went dan Prinsen Geerligs yang diisolasi dari tempe dan telah diidentifikasi berdasarkan karakter fenotipik (morfologi dan fisiologi). Tujuan penelitian adalah melakukan re-identifikasi lima strain R. oryzae (UICC 10, UICC 85, UICC 119, UICC 120, dan UICC 135) berdasarkan data sequence daerah internal transcribed spacers ribosomal DNA dan analisis filogenetik untuk memperoleh identitas spesies yang akurat. Amplifikasi dan sequencing daerah ITS rDNA dilakukan menggunakan primer forward ITS 5 dan primer reverse ITS 4. Data sequence dikirim ke database DNA GenBank untuk pencarian homologi dengan program BLAST. Sequence alignment dilakukan menggunakan program Clustal X. Konstruksi pohon filogenetik dilakukan menggunakan metode Neighbor Joining, model dua parameter Kimura, dan nilai bootstrap 1000 kali pengulangan. Karakterisasi morfologi dan pengujian kemampuan tumbuh pada variasi suhu dilakukan untuk mendukung hasil re-identifikasi dan melengkapi deskripsi strain masing-masing. Hasil amplifikasi daerah ITS rDNA menunjukkan bahwa kelima strain R. oryzae UICC memiliki panjang fragmen dengan ukuran 600--700 pb. Hasil pencarian homologi BLAST menunjukkan bahwa kelima strain memiliki homologi 99,8% terhadap type strain R. oryzae CBS 112.07T. Hasil analisis filogenetik menunjukkan bahwa kelima strain berada dalam satu grup yang monofiletik dengan strain tipe R. oryzae CBS 112.07T dan strain-strain R. oryzae dari database DNA GenBank, dengan dukungan nilai bootstrap yang tinggi (84%). Re-identifikasi lima strain R. oryzae UICC secara molekuler menghasilkan identitas spesies yang sama, yaitu sebagai R. oryzae, dan didukung oleh karakter morfologi dan fisiologi.

---

Universitas Indonesia Culture Collection (UICC) has collection of Rhizopus oryzae Went and Prinsen Geerligs strains, which were isolated from tempeh. These strains were identified based on phenotypic characters (morphology and physiology). The aim of this study was to re-identify five strains of R. oryzae (UICC 10, UICC 85, UICC 119, UICC 120, and UICC 135), based on internal transcribed spacers (ITS) region of ribosomal DNA sequence data to obtain accurate identification at species level.

Amplification and sequencing of ITS region of rDNA were performed using primer set, forward primer ITS 5 and reverse primer ITS 4. The sequence data was sent to GenBank DNA database for homology search using BLAST. Sequence alignment was carried out using Clustal X. Construction of phylogenetic tree was performed using Neighbor Joining method, Kimura's two parameter model and bootstrap values of 1000 iterations. Characterization of the five strains based on morphology and growth ability at temperature variations were carried out to support the description of each strain.

Amplification result showed that the strains have fragment length of ITS region of rDNA about 600--700 bp. Results of BLAST homology search of the strains showed a very high similarity (99.8%) to the type strain R. oryzae CBS 112.07T. Phylogenetic tree showed that the five strains were clustered together in a monophyletic group with the type strain R. oryzae CBS 112.07T and other R. oryzae strains from GenBank DNA database, and supported by high bootstrap value (84%). Re-identification of five strains of R. oryzae UICC based on molecular method showed that they were identified as R. oryzae, similar to previous identification, and supported by morphological and physiological characterization."

"Universitas Indonesia Culture Collection UICC memiliki koleksi Rhizopus spp. yang diisolasi dari tempe dan telah diidentifikasi berdasarkan karakter morfologi dan fisiologi. Tujuan penelitian adalah re-identifikasi lima strain R. oligosporus koleksi UICC UICC 27, UICC 40, UICC 51, UICC 67, dan UICC 116 berdasarkan data sequence daerah internal transcribed spacers rDNA dan analisis filogenetik. Amplifikasi dan sequencing daerah ITS rDNA menggunakan pasangan primer forward ITS5 dan primer reverse ITS4. Data sequence daerah ITS rDNA Rhizopus koleksi UICC dikirim ke database GenBank untuk pencarian homologi BLAST terhadap spesies terdekat dengan pembatasan pencarian hanya pada type material. Pembuatan pohon filogenetik menggunakan metode neighbor joining dengan model evolusi dua parameter Kimura, serta bootstrapping dilakukan sebanyak 1000 kali pengulangan. Karakterisasi morfologi makroskopik dan mikroskopik dan fisiologi pertumbuhan pada variasi suhu dilakukan untuk menunjang hasil identifikasi molekuler. Hasil elektroforesis gel produk PCR daerah ITS rDNA menunjukkan kelima strain memiliki ukuran fragmen ITS rDNA pada kisaran 500--700 pb, dan hasil sequencing lengkap daerah ITS rDNA kelima strain menunjukkan panjang berkisar antara 655--658 pb. Hasil BLAST menunjukkan strain UICC 27, UICC 40, UICC 51, dan UICC 67 memiliki homologi 99,2 ; sedangkan strain UICC 116 memiliki homologi 99,8 terhadap type strain R. oryzae CBS 112.07T. Berdasarkan konsep spesies filogenetik, strain UICC 27, UICC 40, UICC 51, dan UICC 67 dapat diidentifikasi sebagai R. delemar karena pada pohon filogenetik berada dalam satu kelompok yang monofiletik dengan type strain R. delemar CBS 120.12T, dengan dukungan nilai bootstrap 90 ; sedangkan strain UICC 116 diidentifikasi sebagai R. oryzae karena pada pohon filogenetik berada dalam satu kelompok yang monofiletik dengan type strain R. oryzae CBS 112.07T , dengan dukungan nilai bootstrap 82 . Hasil penelitian menunjukkan bahwa kedua spesies tidak dapat dibedakan secara morfologi, kelima strain menunjukkan karakter morfologi yang sesuai dengan R. oryzae. Namun demikian, terdapat perbedaan karakter fisiologi antara R. oryzae dan R. delemar, yaitu pertumbuhan pada variasi suhu.

---

Universitas Indonesia Culture Collection UICC has strains collection of Rhizopus spp. which were isolated from tempeh and identified based on phenotypic characters morphology and physiology . The aim of this study was to re identify five strains of R. oligosporus UICC 10, UICC 85, UICC 119, UICC 120, and the UICC 135 , based on internal transcribed spacers region of ribosomal DNA sequence data and phylogenetic analysis. Amplification and sequencing of ITS region of rDNA were performed using primer set forward primer ITS 5 and reverse primer ITS 4. The sequence data was sent to GenBank for homology search using basic local alignment search tool BLAST program, restricted only to type materials. Construction of phylogenetic tree was performed using Neighbor Joining method with Kimura's two parameter evolution model and bootstrapping with 1,000 replicates. Characterization of morphological and physiological growth at variation of temperature data was carried out to support molecular identification results. Gel electrophoresis showed that five strains have fragment length of ITS region of rDNA, about 500 700 bp. Full sequence data of ITS rDNA of five strains showed the length of their ITS rDNA was ranged 655 658 bp. BLAST homology search results showed that UICC 27, UICC 40, UICC 51, and UICC 67 strain have similarity 99,2 to the type strain of R. oryzae CBS 112.07T, whilst UICC 116 strain showed a higher similarity 99,8 to the type strain of R. oryzae CBS 112.07T. Based on phylogenetic species concept, four strains UICC 27, UICC 40, UICC 51, and UICC 67 were identified as R. delemar. They were clustered with the type strain of R. delemar CBS 120.12T in a monophyletic group, and supported by 90 bootstrap value. Another one strain UICC 116 was identified as R. oryzae. It was clustered with the type strain of R. oryzae CBS 112.07T in a monophyletic group and supported by 82 bootstrap value. Morphological characterization results indicated that the two species are indistinguishable and they showed morphological characters that correspond to R. oryzae. However, the physiological characters i.e. growth at temperature variations differ between of R. delemar and R. oryzae."

"Aspergillus section Nigri adalah salah satu kelompok kapang yang memiliki peran penting dalam bidang mikologi pangan, kedokteran, dan bioteknologi. Kapang tersebut merupakan kandidat yang sering digunakan untuk rekayasa genetika dan pemerintah Amerika Serikat melalui Food and Drug Administration (FDA) memberikan status GRAS (Generally Regarded As Safe) dalam penggunaannya di bidang industri dan bioteknologi. Secara sistematika dan taksonomi, kapang Aspergillus section Nigri memiliki sejumlah permasalahan karena kapang tersebut sukar untuk diidentifikasi dan diklasifikasi. Dalam penelitian ini dilakukan identifikasi dan analisis filogenetik terhadap 20 strain Aspergillus section Nigri terseleksi asal Kebun Raya Eka Karya, Bedugul Bali. Identifikasi kapang terseleksi dilakukan melalui pendekatan morfologi dan molekuler. Karakterisasi morfologi dilakukan dengan mengamati karakter fenotip di media CzA, MEA, CYA, MEA37, dan CY20S. Adapun analisis molekuler dilakukan melalui analisis sekuensing gen pada lokus ITS rDNA, gen ß-tubulin dan calmodulin. Analisis filogenetik dilakukan menggunakan analisis statistik neighbor-joining (NJ). Hasil analisis morfologi dalam penelitian ini belum dapat digunakan untuk mengidentifikasi dan membedakan ke-20 strain pada tingkat takson spesies. Hasil analisis molekuler menunjukkan 7 strain memiliki kedekatan secara genotip dengan A. aculeatus pada kisaran homologi 97-99%, 4 strain memiliki kedekatan dengan A. niger pada kisaran homologi 99-100%, dan 9 strain memiliki kedekatan genotip dengan A. tubingensis pada kisaran homologi 97-100%. Hasil analisis molekuler juga menunjukkan 10 strain yaitu P03, P08, P09,P10, P12, P15, P16, P18, P19, dan P20 memiliki homologi yang rendah pada lokus gen ß-tubulin dan calmodulin sehingga secara genotip strain tersebut kemungkinan merupakan kandidat spesies yang berbeda. Hasil tersebut diperkuat oleh hasil analisis filogenetik NJ pada ketiga lokus. Berdasarkan hasil analisis filogenetik multilokus strain P01, P02, P11, dan P17 adalah takson A. tubingensis, strain P04, P05, P06, dan P07 adalah takson A. niger, dan strain P13 dan P14 adalah takson A. aculeatus. Hasil analisis filogenetik juga menunjukkan adanya spesies tersembunyi (cryptic species) dari beberapa strain Aspergillus hitam yang disolasi dari rhizosfer Piper asal Kebun Raya Eka Karya, Bedugul Bali, yaitu strain P03, P08, P09, P10, P12, P15, P16, P18, P19, dan P20.

---

The black aspergilli (Aspergillus section Nigri ) are an important group of species in food mycology, medical mycology, and biotechnology. They are also candidates for genetic manipulation in the biotechnolology industries since A. niger used under certain industrial condition has been granted the GRAS (Generally Regarded As Safe) status by the Food and Drug Administration of the US government. Black aspergilli are one of the more difficult groups regarding classification and identification. In spite of the taxonomy of the Aspergillus species of the Nigri section being regarded as troublesome. This work aimed to identify and analyse the phylogeny of 20 selected strains of black aspergilli from Eka Karya Botanical Garden, Bedugul Bali. Morphological character were observed from culture were grown on CzA, MEA, CYA, MEA37, and CY20S. Meanwhile, molecular analysis have been conducted based on the ITS rDNA, ß-tubulin, and calmodulin genes. Morphological data result are useful for preliminary identification but it did not having been totally effective in describing and elucidating 20 selected strains into species level. Further molecular analysis showed that from 20 selected strains, seven strains have 97-99% similarity with A. aculeatus, four strains have 99-100% similarity with A. niger, and nine strains have 97-100% similarity with A. tubingensis. Based on molecular analysis particularly ß-tubulin and calmodulin genes, 10 strains (P03, P06, P08, P09, P10, P12, P15, P16, P18, P19, and P20) can be presumed as new species because of the low homology value to their closest related species. Based on the phylogenetic analysis strains of P01, P02, P11, and P17 were identified as A. tubingensis; strain P04, P05, P06, and P07 were identified as A. niger, and strain P13 and P14 were identified as A. aculeatus. Ten strains, namely, P03, P08, P09, P10, P12, P15, P16, P18, P19, and P20, form distinct lineage separated from other recognized Aspergillus in this section. Cryptic species probably exist among the Aspergillus section Nigri strains inhabiting Piper rhizosphere from Eka Karya Botanical Garden, Bedugul Bali."

" 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.

---

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."