scholarly journals An Alkaline Phosphatase/Phosphodiesterase, PhoD, Induced by Salt Stress and Secreted Out of the Cells of Aphanothece halophytica, a Halotolerant Cyanobacterium

2011 ◽  
Vol 77 (15) ◽  
pp. 5178-5183 ◽  
Author(s):  
Hakuto Kageyama ◽  
Keshawanand Tripathi ◽  
Ashwani K. Rai ◽  
Suriyan Cha-um ◽  
Rungaroon Waditee-Sirisattha ◽  
...  

ABSTRACTAlkaline phosphatases (APases) are important enzymes in organophosphate utilization. Three prokaryotic APase gene families, PhoA, PhoX, and PhoD, are known; however, their functional characterization in cyanobacteria largely remains to be clarified. In this study, we cloned thephoDgene from a halotolerant cyanobacterium,Aphanothece halophytica(phoDAp). The deduced protein, PhoDAp, contains Tat consensus motifs and a peptidase cleavage site at the N terminus. The PhoDApenzyme was activated by Ca2+and exhibited APase and phosphodiesterase (APDase) activities. Subcellular localization experiments revealed the secretion and processing of PhoDApin a transformed cyanobacterium. Expression of thephoDApgene inA. halophyticacells was upregulated not only by phosphorus (P) starvation but also under salt stress conditions. Our results suggest thatA. halophyticacells possess a PhoD that participates in the assimilation of P under salinity stress.

2013 ◽  
Vol 80 (5) ◽  
pp. 1763-1769 ◽  
Author(s):  
Rungaroon Waditee-Sirisattha ◽  
Hakuto Kageyama ◽  
Warangkana Sopun ◽  
Yoshito Tanaka ◽  
Teruhiro Takabe

ABSTRACTMycosporine-like amino acids (MAAs) are valuable molecules that are the basis for important photoprotective constituents. Here we report molecular analysis of mycosporine-like amino acid biosynthetic genes from the halotolerant cyanobacteriumAphanothece halophytica, which can survive at high salinity and alkaline pH. This extremophile was found to have a unique MAA core (4-deoxygadusol)-synthesizing gene separated from three other genes.In vivoanalysis showed accumulation of the mycosporine-2-glycine but not shinorine or mycosporine-glycine. Mycosporine-2-glycine accumulation was stimulated more under the stress condition of high salinity than UV-B radiation. TheAphanotheceMAA biosynthetic genes also manifested a strong transcript level response to salt stress. Furthermore, the transformedEscherichia coliandSynechococcusstrains expressing four putativeAphanotheceMAA genes under the control of a native promoter were found to be capable of synthesizing mycosporine-2-glycine. The accumulation level of mycosporine-2-glycine was again higher under the high-salinity condition. In the transformedE. colicells, its level was approximately 85.2 ± 0.7 μmol/g (dry weight). Successful production of a large amount of mycosporine in these cells provides a new opportunity in the search for an alternative natural sunscreen compound source.


Life ◽  
2020 ◽  
Vol 10 (3) ◽  
pp. 23 ◽  
Author(s):  
Siripat Ngoennet ◽  
Masaki Honda ◽  
Tanutcha Patipong ◽  
Takashi Hibino ◽  
Rungaroon Waditee-Sirisattha ◽  
...  

The halotolerant cyanobacterium, Halothece sp. PCC 7418, possesses two classes of fructose-1,6-bisphosphate aldolase (FBA): H2846 and H2847. Though class I (CI)-FBA H2846 is thought to be associated with salt tolerance, the regulatory mechanisms, molecular characteristics, and expression profiles between H2846 and class II (CII)-FBA H2847 have scarcely been investigated. Here, we show that the accumulation of the H2846 protein is highly responsive to both up- and down-shock with NaCl, whereas H2847 is constitutively expressed. The activity of CI- and CII-FBA in cyanobacterial extracts is correlated with the accumulation patterns of H2846 and H2847, respectively. In addition, it was found that these activities were inhibited by NaCl and KCl, with CII-FBA activity strikingly inhibited. It was also found that the CI-FBA activity of recombinant H2846 was hindered by salts and that this hindrance could be moderated by the addition of glycine betaine (GB), whereas no moderation occurred with other potential osmoprotectant molecules (proline, sucrose, and glycerol). In addition, a phylogenetic analysis showed that CI-FBAs with higher similarities to H2846 tended to be distributed among potential GB-synthesizing cyanobacteria. Taken together, our results provide insights into the independent evolution of the CI- and CII-FBA gene families, which show distinct expression profiles and functions following salt stress.


2020 ◽  
Vol 202 (7) ◽  
Author(s):  
Tomoya Kozakai ◽  
Ayako Izumi ◽  
Ayako Horigome ◽  
Toshitaka Odamaki ◽  
Jin-zhong Xiao ◽  
...  

ABSTRACT Bacterial promoters consist of core sequence motifs termed –35 and –10 boxes. The consensus motifs are TTGACA and TATAAT, respectively, which were identified from leading investigations on Escherichia coli. However, the consensus sequences are not likely to fit genetically divergent bacteria. The sigma factor of the genus Bifidobacterium has a characteristic polar domain in the N terminus, suggesting the possibility of specific promoter recognition. We reevaluated the structure of Bifidobacterium longum NCC2705 promoters and compared them to other bacteria. Transcriptional start sites (TSSs) of the B. longum NCC2705 strain were identified using transcriptome sequencing (RNA-Seq) analysis to extract promoter regions. Conserved motifs of a bifidobacterial promoter were determined using regions upstream of TSSs and a hidden Markov model. As a result, consensus motifs of the –35 and –10 boxes were TTGTGC and TACAAT, respectively. To assess each base of both motifs, we constructed 37 plasmids based on pKO403-TPCTcon, including the hup promoter connected with a chloramphenicol acetyltransferase as a reporter gene. This reporter assay showed two optimal motifs of the –35 and –10 boxes, namely, TTGNNN and TANNNT, respectively. We further analyzed spacer lengths between the –35 and –10 boxes via a bioinformatics approach. The spacer lengths predominant in bacteria have been generally reported to be approximately 17 bp. In contrast, the predominant spacer lengths in the genus Bifidobacterium and related species were 11 bp, in addition to 17 bp. A reporter assay to assess the spacer lengths indicated that the 11-bp spacer length produced unusually high activity. IMPORTANCE The structures of sigma factors vary among bacterial strains, indicating that recognition rules may also vary. Therefore, we investigated the promoter structure of Bifidobacterium longum NCC2705 using a bioinformatics approach and wet analyses. The most frequent and optimal motifs were similar to other bacterial consensus motifs. The optimal spacer length between the two boxes was reported to be 17 bp. It is widely applied to a bioinformatics approach for other bacteria. Unexpectedly, conserved spacer lengths were 11 bp as well as 17 bp in the genus Bifidobacterium. Moreover, the sigma factor of the genus Bifidobacterium has a characteristic domain in the N terminus which may contribute to the additional functions. Hence, it would be valuable to reevaluate the promoter in other organisms.


Microbiology ◽  
2020 ◽  
Vol 166 (7) ◽  
pp. 659-668
Author(s):  
Ko Ishikawa ◽  
Chihiro Chubachi ◽  
Saeko Tochigi ◽  
Naomi Hoshi ◽  
Seiji Kojima ◽  
...  

Bis-(3′–5′)-cyclic dimeric guanosine monophosphate (c-di-GMP) is a second messenger known to control a variety of bacterial processes. The model cyanobacterium, Synechocystis sp. PCC 6803, has a score of genes encoding putative enzymes for c-di-GMP synthesis and degradation. However, most of them have not been functionally characterized. Here, we chose four genes in Synechocystis (dgcA–dgcD), which encode proteins with a GGDEF, diguanylate cyclase (DGC) catalytic domain and multiple Per-ARNT-Sim (PAS) conserved regulatory motifs, for detailed analysis. Purified DgcA, DgcB and DgcC were able to catalyze synthesis of c-di-GMP from two GTPs in vitro. DgcA had the highest activity, compared with DgcB and DgcC. DgcD did not show detectable activity. DgcA activity was specific for GTP and stimulated by the divalent cations, magnesium or manganese. Full activity of DgcA required the presence of the multiple PAS domains, probably because of their role in protein dimerization or stability. Synechocystis mutants carrying single deletions of dgcA–dgcD were not affected in their growth rate or biofilm production during salt stress, suggesting that there was functional redundancy in vivo. In contrast, overexpression of dgcA resulted in increased biofilm formation in the absence of salt stress. In this study, we characterize the enzymatic and physiological function of DgcA–DgcD, and propose that the PAS domains in DgcA function in maintaining the enzyme in its active form.


1993 ◽  
Vol 20 (6) ◽  
pp. 693 ◽  
Author(s):  
M Ishitani ◽  
T Takabe ◽  
K Kojima ◽  
T Takabe

When cells of the halotolerant cyanobacterium, Aphanothece halophytica were transferred from control culture medium that contained 0.5 M NaCl to a hypersaline medium with either 1.5 M or 2.0 M NaCl, the rate of photosynthetic CO2 fixation fell instantaneously. Subsequently, the photosynthetic activity returned to almost the original level within 1 day. Under salt stress, ultrastructural changes in the cells were observed by electron microscopy, these cells appeared to recover in parallel with the recovery of their photosynthetic activity. However, the intracellular level of glycinebetaine increased more slowly than the recovery of the photosynthetic CO2 fixation. The maximum rate of accumulation of betaine was estimated to be approximately 60 nmol (mg protein)-1 h-1. This rate is at least one order of magnitude greater than rates reported previously in leaves of salt-stressed higher plants. The accumulation of betaine did not take place in the dark. The intracellular level of betaine decreased as a result of the transfer of the cells to a hypo-osmotic NaCl-containing medium. The accumulation of betaine was also induced by an organic osmoticum, sorbitol. Nitrate enhances the accumulation of betaine under salt stress.


PROTOPLASMA ◽  
2019 ◽  
Vol 256 (6) ◽  
pp. 1727-1736
Author(s):  
Daichi Hasegawa ◽  
Kunihide Kito ◽  
Takumi Maeda ◽  
Vandna Rai ◽  
Suriyan Cha-um ◽  
...  

2013 ◽  
Vol 27 (2) ◽  
pp. 151-158 ◽  
Author(s):  
S. Jezierska-Tys ◽  
A. Rutkowska

Abstract The effect of chemicals (Reglone 200 SL and Elastiq 550 EC) on soil microorganisms and their enzymatic activity was estimated. The study was conducted in a field experiment which was set up in the split-block design and comprised three treatments. Soil samples were taken six times, twice in each year of study. The results showed that the application of chemicals generally had no negative effect on the number of soil microorganisms. The application of Reglone 200 SL caused an increase of proteolytic and ureolytic activity and affected the activity of dehydrogenases, acid and alkaline phosphatases in the soil. The soil subjected of Elastiq 550 EC was characterized by lower activity of dehydrogenases, protease, urease and alkaline phosphatase.


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