Melola Discovery

← Melola Discovery

Jurnal SINTA 1

Alkaline Phosphatase Activity of Plant Growth-Promoting Actinomycetes and Their Genetic Diversity Based on the phoD Gene

HAYATI Journal of Biosciences · Vol. 29 No. 3 (2022) · hlm. 360–369

DOI
10.4308/hjb.29.3.360-369
ISSN
2086-4094, 1978-3019
Terbit
2022-03-28
Penerbit
Bogor Agricultural University, Indonesia
Bahasa
eng

Abstrak

Actinomycete is one of the beneficial bacteria groups inhabiting rhizosphere soil. They can promote plant growth through various mechanisms. In the previous study we have isolated rhizosphere actinomycetes from maize rhizosphere with direct plant growth promotion characters. The aims of the present study were to analyze the ability of maize rhizosphere actinomycetes to solubilize phosphate, determine alkaline phosphatase activity, and study their genetic diversity based on phoD gene. Thirteen rhizosphere actinomycete isolates were able to solubilize phosphate at concertation range 55.84±2.27 mg/L to 144.48±5.71 mg/L. The activity of extracellular alkaline phosphatase was exhibited by all maize rhizosphere actinomycetes isolates in various level ranging from 0.08 mU/mL to 0.51 mU/mL. The phoD gene, one of the three homologous genes which encode alkaline phosphatases, was successfully detected in all isolates and identified as alkaline phosphatase D of Streptomyces spp. The partial phoD sequences of the isolates were located within metallophosphatase domain of alkaline phosphatase D. Alignment analysis showed that the deduced amino acid sequences of PhoD were mostly conserved in the isolates and Streptomyces spp. Essential residues involved in the active core arrangement of PhoD which binds metal ion cofactors were conserved. Constructed phylogenetic tree showed that the isolates were divided into two groups within PhoD cluster. PhoD of the isolates and Streptomyces spp. had closer relationship to purple acid phosphatase compared to other homologous PhoA and PhoX which form separate cluster. Generated three-dimensional structure model of partial PhoD had high similarity to alkaline phosphatase D of Bacillus subtilis (2YEQ) and showed overlapping structure based on super-positioning analysis.

Jaringan kolaborasi para penulis

40 penulis · 123 tautan kepenulisan bersama · 29 lintas organisasi · menampilkan 40 yang paling banyak terhubung

Arahkan kursor atau ketuk sebuah nama untuk menyorot rekan penulisnya. Klik dua kali untuk membuka halaman penulis.

  • IPB University
  • Universitas Islam Negeri Maulana Malik Ibrahim
  • Khairun University
  • Sebelas Maret University
  • Indonesian Center for Agricultural Biotechnology and Genetic Resource Research and Development
  • Sriwijaya University
  • University of Göttingen
  • Organisasi lain
  • Afiliasi tidak diketahui
  • Organisasi berbeda
  • Organisasi sama
  • Afiliasi tidak diketahui
  • Garis lebih tebal = lebih banyak artikel bersama · lingkaran lebih besar = lebih banyak artikel
Tampilkan sebagai tabel
Rekan penulisOrganisasiArtikel bersama
Nisa Rachmania MubarikIPB University5
Rika Indri AstutiIPB University4
Munti YuhanaIPB University3
Antonius SuwantoIPB University3
Miftahudin MiftahudinIPB University3
Anja MeryandiniIPB University3
Suryo WiyonoIPB University2
Yulin LestariIPB University2
Abdul MunifIPB University2
Esti PuspitasariIPB University2
Andreas Adhi SatyaAfiliasi tidak diketahui2
Yepy H. RustamAfiliasi tidak diketahui2
Abdjad Asih NawangsihIPB University2
Suharsono SuharsonoIPB University2
Hamim HamimUniversitas Islam Negeri Maulana Malik Ibrahim2
Waode MunaeniKhairun University1
Widanarni WidanarniIPB University1
Mia SetiawatiIPB University1
Bramantyo Jati PrasojoIPB University1
QatrunnadaIPB University1
Ari SusilowatiSebelas Maret University1
Alina AkhdiyaIndonesian Center for Agricultural Biotechnology and Genetic Resource Research and Development1
Latifah Kosim DarusmanIPB University1
Utut WidyastutiIPB University1
Windarti WahyuningtyasIPB University1
Marini WijayantiSriwijaya University1
Martin EngelhauptUniversity of Göttingen1
İman RusmanaIPB University1
Yuli Siti FatmaIPB University1
Laksmi AmbarsariIPB University1
Rury Eryna PutriIPB University1
Jun NomuraChiba University1
Uci CahliaIPB University1
Siti SholekhaIPB University1
Akhmad Endang Zainal HasanIPB University1
Sri BudiartiIPB University1

Afiliasi berasal dari OpenAlex; metadata OAI-PMH jurnal tidak memuatnya. Penulis tanpa ID OpenAlex dicocokkan berdasarkan nama, sehingga dua orang bisa tergabung atau satu orang bisa terpisah.

Sumber metadata: OAI-PMH (metadata jurnal) http://journal.ipb.ac.id/index.php/hayati/oai, pertama di-harvest 8 Nov 2026, terakhir terlihat 8 Nov 2026.
Metadata asli (oai_dc)
<oai_dc:dc xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/  http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
	<dc:title xml:lang="en">Alkaline Phosphatase Activity of Plant Growth-Promoting Actinomycetes and Their Genetic Diversity Based on the phoD Gene</dc:title>
	<dc:creator xml:lang="en">Amri, Muhammad Faiz</dc:creator>
	<dc:creator xml:lang="en">Husen, Edi</dc:creator>
	<dc:creator xml:lang="en">Tjahjoleksono, Aris</dc:creator>
	<dc:creator xml:lang="en">Wahyudi, Aris Tri</dc:creator>
	<dc:description xml:lang="en">Actinomycete is one of the beneficial bacteria groups inhabiting rhizosphere soil. They can promote plant growth through various mechanisms. In the previous study we have isolated rhizosphere actinomycetes from maize rhizosphere with direct plant growth promotion characters. The aims of the present study were to analyze the ability of maize rhizosphere actinomycetes to solubilize phosphate, determine alkaline phosphatase activity, and study their genetic diversity based on phoD gene. Thirteen rhizosphere actinomycete isolates were able to solubilize phosphate at concertation range 55.84±2.27 mg/L to 144.48±5.71 mg/L. The activity of extracellular alkaline phosphatase was exhibited by all maize rhizosphere actinomycetes isolates in various level ranging from 0.08 mU/mL to 0.51 mU/mL. The phoD gene, one of the three homologous genes which encode alkaline phosphatases, was successfully detected in all isolates and identified as alkaline phosphatase D of Streptomyces spp. The partial phoD sequences of the isolates were located within metallophosphatase domain of alkaline phosphatase D. Alignment analysis showed that the deduced amino acid sequences of PhoD were mostly conserved in the isolates and Streptomyces spp. Essential residues involved in the active core arrangement of PhoD which binds metal ion cofactors were conserved. Constructed phylogenetic tree showed that the isolates were divided into two groups within PhoD cluster. PhoD of the isolates and Streptomyces spp. had closer relationship to purple acid phosphatase compared to other homologous PhoA and PhoX which form separate cluster. Generated three-dimensional structure model of partial PhoD had high similarity to alkaline phosphatase D of Bacillus subtilis (2YEQ) and showed overlapping structure based on super-positioning analysis.</dc:description>
	<dc:publisher xml:lang="en">Bogor Agricultural University, Indonesia</dc:publisher>
	<dc:date>2022-03-28</dc:date>
	<dc:type>info:eu-repo/semantics/article</dc:type>
	<dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
	<dc:type xml:lang="en">Peer-reviewed Article</dc:type>
	<dc:format>application/pdf</dc:format>
	<dc:identifier>http://journal.ipb.ac.id/hayati/article/view/37992</dc:identifier>
	<dc:identifier>10.4308/hjb.29.3.360-369</dc:identifier>
	<dc:source xml:lang="en">HAYATI Journal of Biosciences; Vol. 29 No. 3 (2022): May 2022; 360-369</dc:source>
	<dc:source>2086-4094</dc:source>
	<dc:source>1978-3019</dc:source>
	<dc:language>eng</dc:language>
	<dc:relation>http://journal.ipb.ac.id/hayati/article/view/37992/23192</dc:relation>
	<dc:rights xml:lang="en">Copyright (c) 2022 Muhammad Faiz Amri, Edi Husen, Aris Tjahjoleksono, Aris Tri Wahyudi</dc:rights>
</oai_dc:dc>