Identification of the gene for disaggregatase from Methanosarcina mazei
The gene sequences encoding disaggregatase (Dag), the enzyme responsible for dispersion of cell aggregates of Methanosarcina mazei to single cells, were determined for three strains of M. mazei (S-6T, LYC and TMA). The dag genes of the three strains were 3234 bp in length and had almost the same seq...
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Series: | Archaea |
Online Access: | http://dx.doi.org/10.1155/2008/949458 |
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doaj-504d1c9ecffc42f5b82f5f1334151e692021-07-02T03:02:58ZengHindawi LimitedArchaea1472-36461472-36542008-01-012318519110.1155/2008/949458Identification of the gene for disaggregatase from Methanosarcina mazeiNaoki Osumi0Yoshihiro Kakehashi1Shiho Matsumoto2Kazunari Nagaoka3Junichi Sakai4Kiyotaka Miyashita5Makoto Kimura6Susumu Asakawa7Graduate School of Bioagricultural Sciences, Nagoya University, Nagoya 464-8601, JapanGraduate School of Bioagricultural Sciences, Nagoya University, Nagoya 464-8601, JapanGraduate School of Bioagricultural Sciences, Nagoya University, Nagoya 464-8601, JapanKyushu National Agricultural Experiment Station, Nishigoshi 861-1192, JapanKyushu National Agricultural Experiment Station, Nishigoshi 861-1192, JapanNational Institute of Agro-environmental Sciences, Tsukuba 305-8604, JapanGraduate School of Bioagricultural Sciences, Nagoya University, Nagoya 464-8601, JapanGraduate School of Bioagricultural Sciences, Nagoya University, Nagoya 464-8601, JapanThe gene sequences encoding disaggregatase (Dag), the enzyme responsible for dispersion of cell aggregates of Methanosarcina mazei to single cells, were determined for three strains of M. mazei (S-6T, LYC and TMA). The dag genes of the three strains were 3234 bp in length and had almost the same sequences with 97% amino acid sequence identities. Dag was predicted to comprise 1077 amino acid residues and to have a molecular mass of 120 kDa containing three repeats of the DNRLRE domain in the C terminus, which is specific to the genus Methanosarcina and may be responsible for structural organization and cell wall function. Recombinant Dag was overexpressed in Escherichia coli and preparations of the expressed protein exhibited enzymatic activity. The RT-PCR analysis showed that dag was transcribed to mRNA in M. mazei LYC and indicated that the gene was expressed in vivo. This is the first time the gene involved in the morphological change of Methanosarcina spp. from aggregate to single cells has been identified.http://dx.doi.org/10.1155/2008/949458 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Naoki Osumi Yoshihiro Kakehashi Shiho Matsumoto Kazunari Nagaoka Junichi Sakai Kiyotaka Miyashita Makoto Kimura Susumu Asakawa |
spellingShingle |
Naoki Osumi Yoshihiro Kakehashi Shiho Matsumoto Kazunari Nagaoka Junichi Sakai Kiyotaka Miyashita Makoto Kimura Susumu Asakawa Identification of the gene for disaggregatase from Methanosarcina mazei Archaea |
author_facet |
Naoki Osumi Yoshihiro Kakehashi Shiho Matsumoto Kazunari Nagaoka Junichi Sakai Kiyotaka Miyashita Makoto Kimura Susumu Asakawa |
author_sort |
Naoki Osumi |
title |
Identification of the gene for disaggregatase from Methanosarcina mazei |
title_short |
Identification of the gene for disaggregatase from Methanosarcina mazei |
title_full |
Identification of the gene for disaggregatase from Methanosarcina mazei |
title_fullStr |
Identification of the gene for disaggregatase from Methanosarcina mazei |
title_full_unstemmed |
Identification of the gene for disaggregatase from Methanosarcina mazei |
title_sort |
identification of the gene for disaggregatase from methanosarcina mazei |
publisher |
Hindawi Limited |
series |
Archaea |
issn |
1472-3646 1472-3654 |
publishDate |
2008-01-01 |
description |
The gene sequences encoding disaggregatase (Dag), the enzyme responsible for dispersion of cell aggregates of Methanosarcina mazei to single cells, were determined for three strains of M. mazei (S-6T, LYC and TMA). The dag genes of the three strains were 3234 bp in length and had almost the same sequences with 97% amino acid sequence identities. Dag was predicted to comprise 1077 amino acid residues and to have a molecular mass of 120 kDa containing three repeats of the DNRLRE domain in the C terminus, which is specific to the genus Methanosarcina and may be responsible for structural organization and cell wall function. Recombinant Dag was overexpressed in Escherichia coli and preparations of the expressed protein exhibited enzymatic activity. The RT-PCR analysis showed that dag was transcribed to mRNA in M. mazei LYC and indicated that the gene was expressed in vivo. This is the first time the gene involved in the morphological change of Methanosarcina spp. from aggregate to single cells has been identified. |
url |
http://dx.doi.org/10.1155/2008/949458 |
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