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研究生:陳瑋婷
研究生(外文):CHEN, WEI-TING
論文名稱:分離自台灣淡水之四株新種細菌的分類鑑定與特性分析
論文名稱(外文):Taxonomic Identification and Characterization of Four Novel Species Bacteria Isolated from Freshwater in Taiwan
指導教授:陳文明陳文明引用關係
指導教授(外文):CHEN, WEN-MING
口試委員:許世宜張淑貞
口試委員(外文):SHEU, SHIH-YICHANG, SHWU-JEN
口試日期:2017-07-26
學位類別:碩士
校院名稱:國立高雄海洋科技大學
系所名稱:水產食品科學研究所
學門:農業科學學門
學類:食品科學類
論文種類:學術論文
論文出版年:2017
畢業學年度:105
語文別:中文
論文頁數:116
中文關鍵詞:細菌分類學淡水新種細菌
外文關鍵詞:Bacterial taxonomyHymenobacter gummosusRheinheimera riviphilaRheinheimera coeruleaFlavobacterium album
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  本研究採集台灣花蓮、高雄、屏東三個區域之淡水進行菌株的分離與純化,並從中篩選出具有新種潛力的菌株進行分類及鑑定。三個採集地之樣本中共分離出80株菌,其中包含革蘭氏陽性菌29株以及革蘭氏陰性菌51株。透過16S rRNA基因序列分析進行初步鑑定後,判斷菌株ANT-18、KYPC3、TAPG2、TAPW14具有成為新種細菌的潛力,因此將此四株菌作為本論文之主要研究對象,進行進一步的分類與鑑定。

  菌株ANT-18分離自高雄茂林谷龍頭山瀑布水下游 (22°54'39"N 120°41'09"E),為革蘭氏陰性之好氧桿菌,具有滑動性,具莢膜,不具鞭毛。其菌落在R2A培養基上呈西瓜紅色,規則圓形凸起,有光澤並會產生黏液。生長條件為15-37 °C (最適為25 °C),pH範圍為7-8 (最適為pH 7),以及0-1 % NaCl (最適為0 %)。經由16S rRNA基因序列進行親緣關係分析,顯示其隸屬於Hymenobacter屬,並與Hymenobacter ocellatus具有最高相似度 (97.93 %)。其主要脂肪酸包含iso-C15:0、anteiso-C15:0、C18:0、Summed Feature 4 (iso-C17:1 I/anteiso-C17:1 B)。主要醌型為MK-7。主要的多胺為homospermidine (HSPD)。極性脂肪組成包含phosphatidylethanolamine (PE)、兩個unidentified aminophospholipids (APL1-APL2)、一個unidentified aminolipid (AL)、兩個unidentified glycolipid (GL1-GL2) 以及七個unidentified lipids (L1-L7)。DNA G+C含量為63.65 mol%。經DNA-DNA雜交反應顯示菌株ANT-18與Hymenobacter ocellatus之雜合程度低於39 %,根據一系列形態、生理生化特性及遺傳特徵鑑定,證實其為Hymenobacter屬之新種細菌,並將其命名為Hymenobacter gummosus。模式菌株為ANT-18T (= LMG 29477T = KCTC 52166T = BCRC 80966T)。

  菌株KYPC3與TAPG2分別分離自花蓮縣鳳林鎮林榮里的小溪流 (23°48'02"N 121°29'08"E) 以及屏東縣萬安溪 (22°37'21"N 120°38'48"E),兩者皆為革蘭氏陰性之好氧桿菌,具莢膜,具鞭毛。其菌落在R2A培養基上皆呈現奶油色至灰白色,圓形,中心點呈黃綠色至墨綠色。生長條件分別為10-30 °C (最適為20-25 °C) 以及20-37 °C (最適為25-30 °C), pH範圍分別為6-8 (最適為pH 7) 以及7-8 (最適為pH 7),而生長鹽度範圍則分別為0-0.5 % NaCl (最適為0 %)以及0-1.0 % NaCl (最適為0. 5 %)。經16S rRNA基因序列進行親緣關係分析,顯示兩株菌皆隸屬於Rheinheimera屬,KYPC3與Rheinheimera tangshanensis具有最高相似度 (97.84 %),TAPG2則是與Rheinheimera aquatica具有最高相似度 (98.57 %)。其主要脂肪酸皆為C12:0 3-OH、C16:0、Summed Feature 3 (C16:1ω7c/C16:1ω6c)。主要醌型皆為ubiquinone-8 (Q-8)。極性脂肪組成部分,菌株KYPC3為phosphatidylethanolamine (PE)、phosphatidylglycerol (PG)、unidentified aminophospholipid (APL)、unidentified phospholipid (PL)、unidentified lipid (L);菌株TAPG2為phosphatidylethanolamine (PE)、phosphatidylglycerol (PG)、uncharacterized aminophospholipids (APL)、unidentified aminolipid (AL)、unidentified phospholipid (PL) 以及uncharacterized lipid (L)。DNA G+C含量分別為51.15 mol% 和53.57 mol%。經過DNA-DNA 雜交反應顯示菌株KYPC3和TAPG2與Rheinheimera屬中鄰近模式菌株之間的雜合程度皆低於40 %,根據一系列形態、生理生化特性及遺傳特徵鑑定,證實菌株KYPC3和TAPG2為Rheinheimera屬之新種細菌,並將KYPC3命名為Rheinheimera riviphila,TAPG2命名為Rheinheimera coerulea。模式菌株分別為KYPC3T (= LMG 29729T = KCTC 52440T = BCRC 81008T )以及TAPG2T (= LMG 30056T = KCTC 52815T = BCRC 81054T)。

  菌株TAPW14分離自屏東縣萬安溪 (22°37'21"N 120°38'48"E),為革蘭氏陰性之好氧桿菌,不具莢膜,不具鞭毛。其菌落在R2A培養基上呈現灰白色的半透明不規則粘液狀。生長條件為15-30 °C (最適為25-30 °C), pH範圍為6-8 (最適為pH 7),以及0-2 % NaCl (最適為0.5 %)。由16S rRNA基因序列進行親緣關係分析,顯示其隸屬於Flavobacterium屬,並與Flavobacterium akiainvivens具有最高相似度 (96.54 %)。其主要脂肪酸包含iso-C15:0、C16:0、Summed Feature 3 (C16:1ω7c/C16:1ω6c)。主要醌型為menaquinone-6 (MK-6)。極性脂肪組成包含phosphatidylethanolamine (PE)、uncharacterized aminophospholipids (APL1-APL3)、uncharacterized lipids (L1-L2)。DNA G+C含量為45.97 mol%。經過一系列形態、生理生化特性及遺傳特徵鑑定,證實菌株TAPW14為Flavobacterium屬之新種細菌,並命名為Flavobacterium album。模式菌株為TAPW14T (= LMG 30057T = KCTC 52808T = BCRC 81055T)。

In this study, four novel species bacteria isolated from freshwater in three cities of Taiwan (Hualien, Kaohsiung and Pingtung) were identified and classified.

Strain ANT-18T, isolated from a water sample taken from Longtoushan, Maolin Valley, Kaohsiung City in Taiwan (22°54'39"N 120°41'09"E), was characterized taxonomically using a polyphasic approach. Cells of strain ANT-18T were Gram-stain-negative, aerobic, motile by gliding rods that were covered by large capsules and formed red colonies. Growth occurred at 15-37 °C (optimum 25 °C), at pH 7-8 (optimum pH 7) and with 0-1 % NaCl (optimum 0 %). Phylogenetic analyses based on 16S rRNA gene sequences showed that strain ANT-18T belonged to the genus Hymenobacter and was most closely related to Hymenobacter ocellatus Myx 2105T with a sequence similarity of 97.93 %. The predominant fatty acids contained iso-C15:0, anteiso-C15:0, C18:0 and Summed Feature 4 (iso-C17:1 I/anteiso-C17:1 B). The major isoprenoid quinone was MK-7. The polar lipid profile consisted of phosphatidylethanolamine, two unidentified aminophospholipids, an unidentified glycolipid and seven unidentified lipids. The major polyamine was homospermidine. The DNA G+C content of the genomic DNA was 63.65 mol%. The DNA-DNA relatedness of strain ANT-18T with respect to Hymenobacter ocellatus Myx 2105T was less than 39 %. On the basis of the phylogenetic inference and phenotypic data, strain ANT-18T represents a novel species of the genus Hymenobacter, for which the name Hymenobacter gummosus sp. nov. is proposed. The type strain is ANT-18T (=LMG 29477T = KCTC 52166T = BCRC 80966T).

Bacterial strains KYPC3T and TAPG2T, isolated from water samples taken from Fenglin Township, Hualien County and Wan-An creek, Pingtung County in Taiwan, were characterized taxonomically using a polyphasic approach. Cells of strains KYPC3T and TAPG2T were Gram-stain-negative, aerobic, off-white with yellow-green to dark-green centres, rod-shaped, and motile by means of a single polar flagellum. Growth of strain KYPC3T occurred at 10-30 °C (optimum, 20-25 °C), at pH 6-8 (optimum, pH 7) and with 0-0.5 % NaCl (optimum, 0 %). Growth of strain TAPG2T occurred at 20-37 °C (optimum, 25-30 °C), at pH 7-8 (optimum, pH 7) and with 0-1 % NaCl (optimum, 0 %). Phylogenetic analyses based on 16S rRNA gene sequences showed that strains KYPC3T and TAPG2T were belonged to genus Rheinheimera. Strain KYPC3T was most closely related to Rheinheimera tangshanensis JA3-B52T with sequence similarity of 97.84 %, and strain TAPG2T was most closely related to Rheinheimera aquatica GR5T with sequence similarity of 98.57 %. The major fatty acids of strains KYPC3T and TAPG2T were C12:0 3-OH, C16:0, Summed Feature 3 (C16:1ω7c/C16:1ω6c). The major respiratory quinone of both strains was Q-8. The DNA G+C content of the genomic DNA of both strains was 51.15 mol% and 53.57 mol%, respectively. The polar lipid profile of KYPC3T consisted of a mixture of phosphatidylethanolamine, phosphatidylglycerol, an unidentified phospholipid, an unidentified aminophospholipid and an unidentified lipid; TAPG2T consisted of phosphatidylethanolamine、phosphatidylglycerol、an uncharacterized aminophospholipids、an unidentified aminolipid、an unidentified phospholipid and an uncharacterized lipid. The DNA-DNA relatedness of strains KYPC3T and TAPG2T with respect to recognized members of the genus Rheinheimera were less than 37 %. On the basis of the genotypic, chemotaxonomic and phenotypic data, strains KYPC3T and TAPG2T represent two novel species in the genus Rheinheimera, for which the name Rheinheimera riviphila sp. nov. and Rheinheimera coerulea sp. nov. are proposed, respectively. The type strains are KYPC3T (=LMG 29729T = KCTC 52440T = BCRC 81008T) and TAPG2T (= LMG 30056T = KCTC 52815T = BCRC 81054T).

Strain TAPW14T, isolated from a water sample taken from Wan-An creek, Pingtung County in Taiwan, was characterized taxonomically using a polyphasic approach. Cells of strain TAPW14T were Gram-negative rods, aerobic, no flagella. Flexirubin-type pigments were not produced. Growth occurred at 15-30 °C (optimum 25-30 °C), at pH 6-8 (optimum pH 7) and with 0-2% NaCl (optimum 0.5%). Based on phylogenetic analyses of 16S rRNA gene sequences, the closest neighbour of strain TAPW14T was Flavobacterium akiainvivens IK-1T with 96.54% identity. The predorminant fatty acids of TAPW14T were iso-C15:0, C16:0 and Summed Feature 3 (C16:1ω7c/C16:1ω6c). The polar lipid profile consisted of phosphatidylethanolamine, three unidentified aminophospholipids and two unidentified lipids. The major respiratory quinone was MK-6. The G+C content of the genomic DNA was 45.97 mol%. Based on distance from its nearest phylogenetic neighbours and phenotypic differences, the species Flavobacterium album sp. nov. is proposed to accommodate strain TAPW14T (= LMG 30057T = KCTC 52808T = BCRC 81055T ) as the type strain.

摘要 I
Abstract IV
致謝 VIII
目錄 X
圖目錄 XIV
表目錄 XVI
第一章 緒論 1
一、前言 1
二、研究目的 2
第二章 文獻回顧 3
一、細菌分類學 3
(一) 簡介 3
(一) 歷史發展 3
(二) 分類方式 5
(三) 新菌種/屬之定義標準 6
(四) 正式命名 6
(五) 新種/屬細菌之發表 7
二、菌屬介紹 7
(一) Hymenobacter屬 7
(二) Rheinheimera屬 8
(三) Flavobacterium屬 8
第三章 材料與方法 10
一、實驗架構與流程 10
二、菌株之分離純化與保存 11
(一) 樣品來源 11
(二) 菌株之分離與純化 11
(三) 菌株保存 12
三、細菌形態學分析 13
(一) 菌落形態特徵 13
(二) 菌體形態特徵 15
(三) 運動性觀察 20
四、細菌細胞蛋白質電泳圖譜分析與分群 20
(一) 樣品製備與處理 21
(二) SDS-PAGE分析 22
(三) 電泳膠片之保存與分析 23
五、遺傳特徵分析 24
(一) 16S rRNA基因序列分析與比對 24
(二) 建立演化樹 27
(三) DNA-DNA雜交 (DNA-DNA hybridization) 27
(四) DNA G+C組成分析 30
六、生理特性分析 31
(一) 最適生長條件 31
(二) 氧氣需求測試 - 厭氧缸測試法 32
(三) 抗生素感受性測試 33
七、生化特性分析 34
(一) 氧化酶試驗 34
(二) 觸酶試驗 35
(三) 水解能力測試 35
(四) Biomerieux微生物鑑定套組 38
(五) BIOLOG GN II碳源利用鑑定 44
(六) 色素分析 46
(七) 極性脂肪組成分析 46
(八) 脂肪酸組成分析 49
(九) 多胺分析 51
(十) 醌分析 54
第四章 結果與討論 57
一、菌株分離純化與初步鑑定 57
二、菌株ANT-18之分類鑑定 59
(一) 形態特徵分析 59
(二) 生理特徵分析 60
(三) 生化特徵分析 62
(四) 遺傳特徵分析 70
(五) 與同屬鄰近菌株之差異比較 71
三、菌株KYPC3與TAPG2之分類鑑定 73
(一) 形態特徵分析 73
(二) 生理特徵分析 75
(三) 生化特徵分析 77
(四) 遺傳特徵分析 84
(五) 與同屬鄰近菌株之差異比較 87
四、菌株TAPW14之分類鑑定 89
(一) 形態特徵分析 89
(二) 生理特徵分析 91
(三) 生化特徵分析 93
(四) 遺傳特徵分析 99
(六) 與同屬鄰近菌株之差異比較 101
第五章 結論 103
第六章 參考文獻 108


Azvolinsky, A. (2015). Lost Colonies. The scientist Magazine.
Benson, H. J. (2002). Microbiological Applications. A laboratory Manual in General Microbiology. Published by McGraw Hill, Boston, MA.

Bergey, D. H., Harrison, F. C., Breed, R. S., Hammer, B. W. & Huntoon, F. M. (1923). Bergey's Manual of Determinative Bacteriology. Edition: 1, Baltimore: The Williams & Wilkins Co.

Bowman, J. P. (2000). Description of Cellulophaga algicola sp. nov., isolated from the surfaces of Antarctic algae, and reclassification of Cytophaga uliginosa (ZoBell and Upham 1944) Reichenbach 1989 as Cellulophaga uliginosa comb. nov. Int J Syst Evol Microbiol 50, 1861-1868.

Brettar, I., Christen, R. & Höfle, M. G. (2002). Rheinheimera baltica gen. nov., sp. nov., a blue-coloured bacterium isolated from the central Baltic Sea. Int J Syst Evol Microbiol 52, 1851-1857.

Breznak, J. A. & Costilow, R. N. (2007). Physicochemical factors in growth. In Methods for General and Molecular Bacteriology, 3rd pp. 309-329. Edited by T. J. Beveridge, J. A. Breznak, G. A. Marzluf, T. M. Schmidt & L. R. Snyder. Washington, DC: American Society for Microbiology.

Busse, J., Auling, G. (1988). Polyamine Pattern as a Chemotaxonomic Marker within the Proteobacteria. Int J Syst Evol Microbiol 11, 1-8.

Chen, W. M., Chen, Z. H., Young, C. C. & Sheu, S. Y. (2016). Hymenobacter paludis sp. nov., isolated from a marsh. Int J Syst Evol Microbiol 66, 1546-1553.

Chen, W. M., Lin, C. Y., Young, C. C. & Sheu, S. Y. (2010). Rheinheimera aquatica sp. nov., an antimicrobial activity producing bacterium isolated from freshwater culture pond. J Microbiol Biotechnol 20, 1386-1392.

Chen, W. M., Yang, S. H., Young, C. C. & Sheu, S. Y. (2013). Rheinheimera tilapiae sp. nov., isolated from a freshwater culture pond. Int J Syst Evol Microbiol 63, 1457-1463.

Collins, M. D. (1994). Isoprenoid quinones. In Chemical Methods in Prokaryotic Systematics, pp. 265-309. Edited by M. Goodfellow & A. G. O’Donnell. Chichester: Wiley.

Dong, K., Xu, B., Zhu, F. & Wang, G. (2013). Flavobacterium hauense sp. nov., isolated from soil and emended descriptions of Flavobacterium subsaxonicum , Flavobacterium beibuense and Flavobacterium rivuli. Int J Syst Evol Microbiol 63, 3237-3242.

Embley, T. M. & Wait, R. (1994). Structural lipids of eubacteria. In Chemical Methods in Prokaryotic Systematics, pp. 121-161. Edited by M. Goodfellow & A. G. O’Donnell. Chichester: Wiley.

Euzeby, J. P. (1997). List of Bacterial Names with Standing in Nomenclature: a folder available on the Internet. Int J Syst Bacteriol 47, 590-592. (List of Prokaryotic names with Standing in Nomenclature. http://www.bacterio.net).

Ezaki, T., Hashimoto, Y. & Yabuuchi, E. (1989). Fluorometric deoxyribonucleic acid-deoxyribonucleic acid hybridization in microdilution wells as an alternative to membrane filter hybridization in which radioisotopes are used to determine genetic relatedness among bacterial strains. Int J Syst Bacteriol 39, 224-229.

Felsenstein, J. (1981). Evolutionary trees from DNA sequences: a maximum likelihood approach. J Mol Evol 17, 368-376.

Gerhardt, P. (1994). Methods for General and Molecular Bacteriology. Washington, D.C.: American Society for Microbiology.

Glaeser, S. P. & Kämpfer, P. (2015). Multilocus sequence analysis (MLSA) in prokaryotic taxonomy. Syst Appl Microbiol 38, 237-245.

Hall, T. A. (1999). BioEdit: a user-friendly biological sequence alignment editor and analysis program for Windows 95/98/NT. Nucleic Acids Symposium Series 41, 95-98.

Heimbrook, M. E., Wang, W. L. & Campbell, G. (1989). Staining bacterial flagella easily. J Clin Microbiol, 27, 2612-2615.

Hirsch, P., Ludwig, W., Hethke, C., Sittig, M., Hoffmann, B. & Gallikowski, C. A. (1998). Hymenobacter roseosalivarius gen. nov., sp. nov. from continental Antarctic soils and sandstone: bacteria of the Cytophaga/Flavobacterium/Bacteroides line of phylogenetic descent. Syst Appl Microbiol 21, 374-383.

Hsu, S. C. & Lockwood, J. L. (1975). Powdered chitin agar as a selective medium for enumeration of Actinomycetes in water and soil. Appl Microbiol 29, 422-426.

Kang, J. Y., Chun, J., Choi, A., Moon, S. H., Cho, J. C. & Jahng, K. Y. (2013). Hymenobacter koreensis sp. nov. and Hymenobacter saemangeumensis sp. nov., isolated from estuarine water. Int J Syst Evol Microbiol 63, 4568-4573.

Kim, O. S., Cho, Y. J., Lee, K., Yoon, S. H., Kim, M., Na, H., Park, S. C., Jeon, Y. S., Lee, J. H., Yi, H., Won, S. & Chun, J. (2012). Introducing EzTaxon-e: a prokaryotic 16S rRNA gene sequence database with phylotypes that represent uncultured species. Int J Syst Evol Microbiol 62, 716-721.

Kluge, A. G. & Farris, F. S. (1969). Quantitative phyletics and the evolution of anurans. Syst Zool 18, 1-32.

Kuo, I., Saw, J., Kapan, D. D., Christensen, S., Kaneshiro, K. Y. & Donachie, S. P. (2013). Flavobacterium akiainvivens sp. nov., from decaying wood of Wikstroemia oahuensis, Hawai‘i, and emended description of the genus Flavobacterium. Int J Syst Evol Microbiol 63, 3280-3286.

Kumar, S., Stecher, G. & Tamura, K. (2016). MEGA7: Molecular evolutionary genetics analysis version 7.0 for bigger datasets. Mol Biol Evol 33, 1870-1874.

Kumar, A., Bajaj, A., Mathan, K. R., Kaur, G., Kaur, N., Kumar, S. N., Manickam, N. & Mayilraj, S. (2015). Taxonomic description and genome sequence of Rheinheimera mesophila sp. nov., isolated from an industrial waste site. sequence database with phylotypes that represent uncultured species. Int J Syst Evol Microbiol 65, 3666-3673.

Locey, K. J. & Lennon, J. T. (2016). Scaling laws predict global microbial diversity. Proc Natl Acad Sci U S A. 113, 5970-5975.

Malka, H., Yigal, S. & Sagi, S. (2007). Rheinheimera chironomi sp. nov., isolated from a chironomid (Diptera; Chironomidae) egg mass. Int J Syst Evol Microbiol 57, 1872-1875.

Marmur, J. & Doty, P. (1962). Determination of the base composition of deoxyribonucleic acid from its thermal denaturation temperature. J Mol Biol 5, 109-118.

Mubina, M. M., Allana, K. W. & Robert, J. C. M. (2007). Rheinheimera texasensis sp. nov., a halointolerant freshwater oligotroph. Int J Syst Evol Microbiol 57, 2376-2380.

Nokhal, T. H. & Schlegel, H. G. (1983). Taxonomic study of Paracoccus denitrificans. Int J Syst Bacteriol 33, 26-37.

Petri, R. J. (1887). Eine kleine Modification des Koch'schen Plattenverfahrens. Centralblatt für Bakteriologie und Parasitenkund 1, 279-280.

Powers, E. M. (1995). Efficacy of the Ryu nonstaining KOH technique for rapidly determining gram reactions of food-borne and waterborne bacteria and yeasts. Appl Environ Microbiol 61, 3756-3758.

Ryu, S. H., Chung, B. S., Park, M., Lee, S. S., Lee, S. S. & Jeon, C. O. (2008). Rheinheimera soli sp. nov., a gammaproteobacterium isolated from soil in Korea. Int J Syst Evol Microbiol 58, 2271-2274.

Saitou, N. & Nei, M. (1987). The neighbor-joining method: a new method for reconstructing phylogenetic trees. Mol Biol Evol 4, 406-425.

Sandra, B., Ewald, B. M. D., Peter, K. & Hans, J. B. (2006). Proposal of Hymenobacter norwichensis sp. nov., classification of ‘Taxeobacter ocellatus’, ‘Taxeobacter gelupurpurascens’ and ‘Taxeobacter chitinovorans’ as Hymenobacter ocellatus sp. nov., Hymenobacter gelipurpurascens sp. nov. and Hymenobacter chitinivorans sp. nov., respectively, and emended description of the genus Hymenobacter Hirsch et al. 1999. Int J Syst Evol Microbiol 56, 2071-2078.

Schmidt, K., Connor, A. & Britton, G. (1994). Analysis of pigments: carotenoids and related polyenes. In Chemical Methods in Prokaryotic Systematics, pp. 403-461. Edited by M. Goodfellow & A. G. O’Donnell. Chichester: Wiley.

Tindall, B. J., Rosselló-Móra, R., Busse, H. J., Ludwig, W. & Kämpfer, P. (2010). Notes on the characterization of prokaryote strains for taxonomic purposes. Int J Syst Evol Microbiol 60, 249-266.

Wayne, L. G., Brenner, D. J., Colwell, R. R. & 9 other authors. (1987). Report of the ad hoc committee on reconciliation of approaches of bacterial systematics. Int J Syst Bacteriol 37, 463-464.

Weeks, O. B. (1981). Preliminary studies of the pigments of Flavobacterium breve NCTC 11099 and Flavobacterium odoratum NCTC 11036. In Flavobacterium-Cytophaga Group, pp. 108-114. Edited by H. Reichenbach & O. B. Weeks. Weinheim: Gesellschaft fu¨r Biotechnologische Forschung.

Woese, C. R., Kandler, O. & Wheelis, M. L. (1990). Towards a natural system of organisms: proposal for the domains Archaea、Bacteria and Eucarya. Proc Natl Acad Sci USA 87, 4576-4579

Zhang, L., Dai, J., Tang, Y., Luo, X.,Wang, Y., An, H., Fang, C. & Zhang, C. (2009). Hymenobacter deserti sp. nov., isolated from the desert of Xinjiang, China. Int J Syst Evol Microbiol 59, 77-82.

Xu, H. X., Kawamura, Y., Li, N., Zhao, L., Li, T. M., Li, Z. Y., Shu, S. & Ezaki, T. (2000). A rapid method for determining the G+C content of bacterial chromosomes by monitoring fluorescence intensity during DNA denaturation in a capillary tube. Int J Syst Evol Microbiol 50, 1463-1469.

Zhang, X., Sun, L., Qiu, F., McLean, R. J., Jiang, R. & Song, W. (2008). Rheinheimera tangshanensis sp. nov., a rice root-associated bacterium. Int J Syst Evol Microbiol 58, 2420-2424.

郝常明、王德培、丁友昉, 1999。光合細菌中類葫蘿蔔的提取及性質的研究。中國天津輕工業學
院學報 3,5-11。

楊蘇聲,1997。細菌分類學。中國農業大學出版社。

謝文陽,2006。細菌分類的濫觴和演變。科學發展 408,59-67。

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