L. R. L. S. Kumari, A. Senaratne, W. R. P. Wijesinghe
{"title":"为开发生物肥料分离潜在的岩石磷酸盐溶解曲霉菌孢子","authors":"L. R. L. S. Kumari, A. Senaratne, W. R. P. Wijesinghe","doi":"10.4038/cjs.v53i1.8168","DOIUrl":null,"url":null,"abstract":"Phosphorus (P) is one of the key bio elements that limits agricultural production. Although Sri Lanka is endowed with rock phosphate deposits, practical means to utilize this resource are limited. Phosphate-solubilizing fungi (PSF) play an important role in enhancing the bioavailability of soil phosphorus to plants. In this study, fungi from eight soil samples in Kaikawala, Sri Lanka, were isolated using spread plate method and analyzed for its phosphate solubility capacity. One fungal isolate with significant halo zones on Pikovskaya’s agar (PVK) plates, containing 0.5% tricalcium phosphate, was identified. After purification, the isolate was transferred to three media setups: PVK with 0.5% apatite (ERP) as the phosphate source, PVK with 0.5% tricalcium phosphate as a positive control, and PVK without P source as a negative control and analyzed for the solubilization index (SI). DNA sequences of the internal transcribed spacers with 5.8S region of ribosomal DNA (ITS1-5.8S-ITS2) was analyzed with universal primer pair ITS4-F/ITS5-R to determine the identity of the species. Fungal isolate PSF01 showed a phosphate solubilizing activity on both PVK media, ERP (1.07 ± 0.03 cm SI) and tricalcium phosphate (1.07 ± 0.01 cm), with similar effects (p > 0.05). However, the SI in the negative control was 1.00 ± 0.00 cm without halo zone (p < 0.05). The fungal strain is fast growing with initially white but quickly changing to black colonies after producing conidial spores on potato dextrose agar with distinctive conidial heads and pale-yellow lower surface characterized as Aspergillus. Sanger DNA sequencing identified the fungus as Aspergillus niger (99%) and a phylogenetic tree was constructed using MEGA11 software using reference data obtained from NCBI GenBank data to identify the isolated PSF01. Consequently, our preliminary studies demonstrate the importance of examining more soil samples to identify PSF for sustainable agricultural applications in the future.","PeriodicalId":9894,"journal":{"name":"Ceylon Journal of Science","volume":"196 2","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-01-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Isolation of a potential rock phosphate solubilizing Aspergillus sp. towards development of biofertilizer\",\"authors\":\"L. R. L. S. Kumari, A. Senaratne, W. R. P. 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DNA sequences of the internal transcribed spacers with 5.8S region of ribosomal DNA (ITS1-5.8S-ITS2) was analyzed with universal primer pair ITS4-F/ITS5-R to determine the identity of the species. Fungal isolate PSF01 showed a phosphate solubilizing activity on both PVK media, ERP (1.07 ± 0.03 cm SI) and tricalcium phosphate (1.07 ± 0.01 cm), with similar effects (p > 0.05). However, the SI in the negative control was 1.00 ± 0.00 cm without halo zone (p < 0.05). The fungal strain is fast growing with initially white but quickly changing to black colonies after producing conidial spores on potato dextrose agar with distinctive conidial heads and pale-yellow lower surface characterized as Aspergillus. Sanger DNA sequencing identified the fungus as Aspergillus niger (99%) and a phylogenetic tree was constructed using MEGA11 software using reference data obtained from NCBI GenBank data to identify the isolated PSF01. 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引用次数: 0
摘要
磷(P)是限制农业生产的关键生物元素之一。虽然斯里兰卡拥有丰富的磷酸盐岩矿藏,但利用这一资源的实际手段却很有限。磷酸盐溶解真菌(PSF)在提高植物对土壤磷的生物利用率方面发挥着重要作用。在这项研究中,研究人员采用展板法从斯里兰卡凯卡瓦拉的八个土壤样本中分离出真菌,并对其磷酸盐溶解能力进行了分析。其中一个真菌分离物在含有 0.5% 磷酸三钙的皮科夫斯卡娅琼脂(PVK)平板上有明显的光晕区。纯化后,该分离物被转移到三种培养基中:以含 0.5% 磷灰石(ERP)的 PVK 为磷酸盐源,以含 0.5% 磷酸三钙的 PVK 为阳性对照,以不含磷酸盐源的 PVK 为阴性对照,并分析增溶指数(SI)。用通用引物对 ITS4-F/ITS5-R 分析了核糖体 DNA 5.8S 区内部转录间隔(ITS1-5.8S-ITS2)的 DNA 序列,以确定物种的身份。真菌分离物 PSF01 在 PVK 培养基、ERP(1.07 ± 0.03 cm SI)和磷酸三钙(1.07 ± 0.01 cm)上均表现出磷酸盐溶解活性,且效果相似(p > 0.05)。然而,阴性对照的 SI 为 1.00 ± 0.00 厘米,无晕带(p < 0.05)。该真菌菌株生长迅速,在马铃薯葡萄糖琼脂上产生分生孢子后,菌落最初为白色,但很快变为黑色,具有明显的分生孢子头和淡黄色下表面,特征为曲霉。Sanger DNA 测序确定该真菌为黑曲霉(99%),并利用从 NCBI GenBank 数据库中获得的参考数据,使用 MEGA11 软件构建了系统发生树,以确定分离出的 PSF01。因此,我们的初步研究表明,必须对更多的土壤样本进行检测,以确定未来可持续农业应用中的 PSF。
Isolation of a potential rock phosphate solubilizing Aspergillus sp. towards development of biofertilizer
Phosphorus (P) is one of the key bio elements that limits agricultural production. Although Sri Lanka is endowed with rock phosphate deposits, practical means to utilize this resource are limited. Phosphate-solubilizing fungi (PSF) play an important role in enhancing the bioavailability of soil phosphorus to plants. In this study, fungi from eight soil samples in Kaikawala, Sri Lanka, were isolated using spread plate method and analyzed for its phosphate solubility capacity. One fungal isolate with significant halo zones on Pikovskaya’s agar (PVK) plates, containing 0.5% tricalcium phosphate, was identified. After purification, the isolate was transferred to three media setups: PVK with 0.5% apatite (ERP) as the phosphate source, PVK with 0.5% tricalcium phosphate as a positive control, and PVK without P source as a negative control and analyzed for the solubilization index (SI). DNA sequences of the internal transcribed spacers with 5.8S region of ribosomal DNA (ITS1-5.8S-ITS2) was analyzed with universal primer pair ITS4-F/ITS5-R to determine the identity of the species. Fungal isolate PSF01 showed a phosphate solubilizing activity on both PVK media, ERP (1.07 ± 0.03 cm SI) and tricalcium phosphate (1.07 ± 0.01 cm), with similar effects (p > 0.05). However, the SI in the negative control was 1.00 ± 0.00 cm without halo zone (p < 0.05). The fungal strain is fast growing with initially white but quickly changing to black colonies after producing conidial spores on potato dextrose agar with distinctive conidial heads and pale-yellow lower surface characterized as Aspergillus. Sanger DNA sequencing identified the fungus as Aspergillus niger (99%) and a phylogenetic tree was constructed using MEGA11 software using reference data obtained from NCBI GenBank data to identify the isolated PSF01. Consequently, our preliminary studies demonstrate the importance of examining more soil samples to identify PSF for sustainable agricultural applications in the future.