伊拉克土壤样品中Waksman链霉菌和Henrici链霉菌1943株的筛选

Bassam Qasim, M. H. Risan
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引用次数: 1

摘要

背景:链霉菌Waksman & Henrici 1943属包括需氧菌、革兰氏阳性菌和丝状菌,它们产生发育良好的有分支的营养菌丝。胞壁由不同化合物的大混合物组成,包括肽聚糖、锝酸、锝酸和多糖。肽聚糖组分由不规则的n -乙酰-d-氨基戊酸(NAM)、二氨基戊酸、n -乙酰-d-氨基葡萄糖胺(NAG)和DAP链组成,这在原核微生物细胞壁中是独特的。锝酸和锝酸在化学上与肽聚糖结合。方法:取1克土样配制悬浮液,加入无菌蒸馏水(原液悬浮液)99 mL,室温下在摇床中以160转/分摇摇30分钟。从原液混悬液中连续稀释0.1-0.001,静置10分钟。摇匀后,各稀释液0.1 mL用链霉素50 ug/mL在酵母膏和麦芽膏琼脂(YEME)上培养。28℃孵育7 ~ 10天。根据培养特点,选择疑似链霉菌菌落,菌落特征为小、白、尖、粗糙、白垩,周围有明显的抑制区。这些菌落通过革兰氏染色类型、气生和底生菌丝颜色、色素产量和色素颜色进行鉴定。利用国际链霉菌项目(International Streptomyces project, ISP)对链霉菌进行重新条纹检测,获得用于鉴定的纯菌落。结果:本研究旨在筛选链霉菌分离菌。仅21份土壤样品疑似含有链霉菌,每份土壤样品分离到45株不同形态类型的链霉菌。殖民地嫌疑人是根据灰色、白色和乳白色的颜色来选择的。用革兰氏染色法对局部链霉菌进行显微镜检查。结果表明,局部链霉菌革兰氏阳性,具有分枝菌丝体的棒状特征与真菌相似。链霉菌产生额外的细胞酶,如淀粉酶、脲酶、过氧化氢酶、蛋白酶、明胶酶、纤维素酶和磷酸酶。柠檬酸的利用率为正,不产生黑色素反应和可溶性色素,而不产生吲哚。结论:链霉菌的鉴定是一个非常复杂的过程。形态特征和生化特征是链霉菌科分类的两个重要方面。通过形态学、培养和生化特征的研究,发现当地分离株属于链霉菌属。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Screening of bacteria Streptomyces Waksman and Henrici 1943 (Streptomycetaceae) Isolates from Soil Samples in Iraq
Background: The genus Streptomyces Waksman & Henrici 1943 includes aerobic, gram-positive, and filamentous bacteria which produce well developed vegetative hyphae with branches. The wall consists of a large mixture of different compounds, including peptidoglycan, teichuronic acid, teichoic, and polysaccharides. The peptidoglycan components consist of glycan as a chains of irregular N-acetyl- d-muramic acid (NAM), diaminopimelic acid, and N-acetyl-d-glucosamine (NAG) and DAP, which is unique in the cell walls of prokaryotic microorganisms. The teichoic and teichuronic acid are chemically bonded to peptidoglycan. Methods: One gram of soil samples was used to make suspension, by adding 99 mL of sterile distilled water (stock suspension) into it and shaking it in a shaker at 160 rpm for 30 minutes at room temperature. Serial dilutions from 0.1-0.001 were made from the stock suspension, and left for 10 minutes. After shaking, 0.1 mL of each dilution was cultured on Yeast Extract and Malt Extract agar (YEME) with Streptomycin 50 ug/mL. The inoculated plates were incubated at 28 °C for 7 to 10 days. Based on cultural characteristics, suspected colonies of Streptomyces were selected, which are characterized as small, white, pin-point, rough, chalky, and a clear zone of inhibition around them. These colonies were confirmed their identification by types of Gram’s stain, aerial and substrate mycelium color, pigment production, and pigment color.  Streptomyces were re-streaked on International Streptomyces project (ISP) to obtain pure colonies used for identification.   Results: The current study aimed to screen bacteria Streptomyces isolates. Only 21 samples of soil were suspected to contain Streptomyces, and 45 isolates were obtained with different morphology types per samples of soil. The colonies suspects were selected basis on color that ranged from gray, white and creamy. The microscopic examination of local Streptomyces spp. after Gram-staining method was conducted. The observations revealed that local Streptomyces is gram positive and rod shaped similar to features of fungal in possessing branched mycelium. The Streptomyces produced extra cellular enzymes like amylase, urease, catalase, protease, Gelatinase, cellulase and phosphatase. Utilization of citrate was positive, with no Melanine reaction production and soluble pigmented, and negative for indole production. Conclusion: The identification of the Streptomyces is a very complex process.  Morphological and biochemical characteristics are two important aspects for the classification in the Streptomycetaceae family. By studying the morphological, cultural, and biochemical characteristics, it is observed that the local isolates are belonging to the genus of Streptomyces.
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