Adaptive mutation related to cellulose producibility in Komagataeibacter medellinensis ( Gluconacetobacter xylinus ) NBRC 3288

Verfasser / Beitragende:
[Minenosuke Matsutani, Kohei Ito, Yoshinao Azuma, Hidetaka Ogino, Mutsunori Shirai, Toshiharu Yakushi, Kazunobu Matsushita]
Ort, Verlag, Jahr:
2015
Enthalten in:
Applied Microbiology and Biotechnology, 99/17(2015-09-01), 7229-7240
Format:
Artikel (online)
ID: 605503044
LEADER caa a22 4500
001 605503044
003 CHVBK
005 20210128100609.0
007 cr unu---uuuuu
008 210128e20150901xx s 000 0 eng
024 7 0 |a 10.1007/s00253-015-6598-x  |2 doi 
035 |a (NATIONALLICENCE)springer-10.1007/s00253-015-6598-x 
245 0 0 |a Adaptive mutation related to cellulose producibility in Komagataeibacter medellinensis ( Gluconacetobacter xylinus ) NBRC 3288  |h [Elektronische Daten]  |c [Minenosuke Matsutani, Kohei Ito, Yoshinao Azuma, Hidetaka Ogino, Mutsunori Shirai, Toshiharu Yakushi, Kazunobu Matsushita] 
520 3 |a Gluconacetobacter xylinus (formerly Acetobacter xylinum and presently Komagataeibacter medellinensis) is known to produce cellulose as a stable pellicle. However, it is also well known to lose this ability very easily. We investigated the on and off mechanisms of cellulose producibility in two independent cellulose-producing strains, R1 and R2. Both these strains were isolated through a repetitive static culture of a non-cellulose-producing K. medellinensis NBRC 3288 parental strain. Two cellulose synthase operons, types I and II, of this strain are truncated by the frameshift mutation in the bcsBI gene and transposon insertion in the bcsCII gene, respectively. The draft genome sequencing of R1 and R2 strains revealed that in both strains the bcsBI gene was restored by deletion of a nucleotide in its C-rich region. This result suggests that the mutations in the bcsBI gene are responsible for the on and off mechanism of cellulose producibility. When we looked at the genomic DNA sequences of other Komagataeibacter species, several non-cellulose-producing strains were found to contain similar defects in the type I and/or type II cellulose synthase operons. Furthermore, the phylogenetic relationship among cellulose synthase genes conserved in other bacterial species was analyzed. We observed that the cellulose genes in the Komagataeibacter shared sequence similarities with the γ-proteobacterial species but not with the α-proteobacteria and that the type I and type II operons could be diverged from a same ancestor in Komagataeibacter. 
540 |a Springer-Verlag Berlin Heidelberg, 2015 
690 7 |a Acetic acid bacteria  |2 nationallicence 
690 7 |a Komagataeibacter  |2 nationallicence 
690 7 |a Cellulose synthase gene  |2 nationallicence 
700 1 |a Matsutani  |D Minenosuke  |u Department of Biological Chemistry, Faculty of Agriculture, Yamaguchi University, 753-8515, Yamaguchi, Japan  |4 aut 
700 1 |a Ito  |D Kohei  |u Department of Biological Chemistry, Faculty of Agriculture, Yamaguchi University, 753-8515, Yamaguchi, Japan  |4 aut 
700 1 |a Azuma  |D Yoshinao  |u Biology-oriented Science and Technology, Kinki University, Nishimitani 930, 649-6493, Kinokawa, Wakayama, Japan  |4 aut 
700 1 |a Ogino  |D Hidetaka  |u Department of Microbiology and Immunology, Yamaguchi University Graduate School of Medicine, Ube, Yamaguchi, Japan  |4 aut 
700 1 |a Shirai  |D Mutsunori  |u Department of Microbiology and Immunology, Yamaguchi University Graduate School of Medicine, Ube, Yamaguchi, Japan  |4 aut 
700 1 |a Yakushi  |D Toshiharu  |u Department of Biological Chemistry, Faculty of Agriculture, Yamaguchi University, 753-8515, Yamaguchi, Japan  |4 aut 
700 1 |a Matsushita  |D Kazunobu  |u Department of Biological Chemistry, Faculty of Agriculture, Yamaguchi University, 753-8515, Yamaguchi, Japan  |4 aut 
773 0 |t Applied Microbiology and Biotechnology  |d Springer Berlin Heidelberg  |g 99/17(2015-09-01), 7229-7240  |x 0175-7598  |q 99:17<7229  |1 2015  |2 99  |o 253 
856 4 0 |u https://doi.org/10.1007/s00253-015-6598-x  |q text/html  |z Onlinezugriff via DOI 
898 |a BK010053  |b XK010053  |c XK010000 
900 7 |a Metadata rights reserved  |b Springer special CC-BY-NC licence  |2 nationallicence 
908 |D 1  |a research-article  |2 jats 
949 |B NATIONALLICENCE  |F NATIONALLICENCE  |b NL-springer 
950 |B NATIONALLICENCE  |P 856  |E 40  |u https://doi.org/10.1007/s00253-015-6598-x  |q text/html  |z Onlinezugriff via DOI 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Matsutani  |D Minenosuke  |u Department of Biological Chemistry, Faculty of Agriculture, Yamaguchi University, 753-8515, Yamaguchi, Japan  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Ito  |D Kohei  |u Department of Biological Chemistry, Faculty of Agriculture, Yamaguchi University, 753-8515, Yamaguchi, Japan  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Azuma  |D Yoshinao  |u Biology-oriented Science and Technology, Kinki University, Nishimitani 930, 649-6493, Kinokawa, Wakayama, Japan  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Ogino  |D Hidetaka  |u Department of Microbiology and Immunology, Yamaguchi University Graduate School of Medicine, Ube, Yamaguchi, Japan  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Shirai  |D Mutsunori  |u Department of Microbiology and Immunology, Yamaguchi University Graduate School of Medicine, Ube, Yamaguchi, Japan  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Yakushi  |D Toshiharu  |u Department of Biological Chemistry, Faculty of Agriculture, Yamaguchi University, 753-8515, Yamaguchi, Japan  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Matsushita  |D Kazunobu  |u Department of Biological Chemistry, Faculty of Agriculture, Yamaguchi University, 753-8515, Yamaguchi, Japan  |4 aut 
950 |B NATIONALLICENCE  |P 773  |E 0-  |t Applied Microbiology and Biotechnology  |d Springer Berlin Heidelberg  |g 99/17(2015-09-01), 7229-7240  |x 0175-7598  |q 99:17<7229  |1 2015  |2 99  |o 253