Cloning and expression analysis of tps, and cryopreservation research of trehalose from Antarctic strain Pseudozyma sp.

Trehalose is a non-reducing disaccharide sugar that widely exists in a variety of organisms, such as bacteria and eukaryotes except the vertebrates. It plays an important role in a number of critical metabolic functions especially in response to stressful environmental conditions. However, the biosy...

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Published in:3 Biotech
Main Authors: Yin, Hua, Wang, Yibin, He, Yingying, Xing, Lei, Zhang, Xiufang, Wang, Shuai, Qi, Xiaoqing, Zheng, Zhou, Lu, Jian, Miao, Jinlai
Format: Text
Language:English
Published: Springer Berlin Heidelberg 2017
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Online Access:http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5610133/
http://www.ncbi.nlm.nih.gov/pubmed/28955640
https://doi.org/10.1007/s13205-017-0983-3
id ftpubmed:oai:pubmedcentral.nih.gov:5610133
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spelling ftpubmed:oai:pubmedcentral.nih.gov:5610133 2023-05-15T13:41:08+02:00 Cloning and expression analysis of tps, and cryopreservation research of trehalose from Antarctic strain Pseudozyma sp. Yin, Hua Wang, Yibin He, Yingying Xing, Lei Zhang, Xiufang Wang, Shuai Qi, Xiaoqing Zheng, Zhou Lu, Jian Miao, Jinlai 2017-09-22 http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5610133/ http://www.ncbi.nlm.nih.gov/pubmed/28955640 https://doi.org/10.1007/s13205-017-0983-3 en eng Springer Berlin Heidelberg http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5610133/ http://www.ncbi.nlm.nih.gov/pubmed/28955640 http://dx.doi.org/10.1007/s13205-017-0983-3 © Springer-Verlag GmbH Germany 2017 Original Article Text 2017 ftpubmed https://doi.org/10.1007/s13205-017-0983-3 2018-10-07T00:12:09Z Trehalose is a non-reducing disaccharide sugar that widely exists in a variety of organisms, such as bacteria and eukaryotes except the vertebrates. It plays an important role in a number of critical metabolic functions especially in response to stressful environmental conditions. However, the biosynthetic pathways of trehalose in cold-adapted yeast and its responses to temperature and salinity changes remain little understood. In this study, the genome of Antarctic-isolated Pseudozyma sp. NJ7 was generated from which we identified the gene coding for trehalose phosphate synthase (TPS1) and trehalose phosphate phosphatase (TPS2), the two enzymes most critical for trehalose production. The whole draft genome length of Pseudozyma sp. NJ7 was 18,021,233 bp, and encoded at least 34 rRNA operons and 72 tRNAs. The open reading frame of tps1 contained 1827 nucleotide encoding 608 amino acids with a molecular weight of 67.64 kDa, and an isoelectric point of 5.54, while tps2 contained 3948 nucleotide encoding 1315 amino acids with a molecular weight of 144.47 kDa and an isoelectric point of 6.36. The TPS1 and TPS2 protein sequences were highly homologous to Moesziomyces antarcticus T-34, but TPS2 had obvious specificity and differently with others which suggest species specificity and different evolutionary history. Expression level of tps1 gene was strongly influenced by temperature and high salinity. In addition, addition of 0.5% trehalose preserved yeast cells in the short term but was not effective for cryopreservation for more than 5 days, but still suggesting that exogenous trehalose could indeed significantly improve the survival of yeast cells under freezing conditions. Our results provided new insights on the molecular basis of cold adaptations of Antarctic Pseudozyma sp., and also generated new information on the roles trehalose play in yeast tolerance to extreme conditions in the extreme Antarctic environments. Text Antarc* Antarctic antarcticus PubMed Central (PMC) Antarctic 3 Biotech 7 5
institution Open Polar
collection PubMed Central (PMC)
op_collection_id ftpubmed
language English
topic Original Article
spellingShingle Original Article
Yin, Hua
Wang, Yibin
He, Yingying
Xing, Lei
Zhang, Xiufang
Wang, Shuai
Qi, Xiaoqing
Zheng, Zhou
Lu, Jian
Miao, Jinlai
Cloning and expression analysis of tps, and cryopreservation research of trehalose from Antarctic strain Pseudozyma sp.
topic_facet Original Article
description Trehalose is a non-reducing disaccharide sugar that widely exists in a variety of organisms, such as bacteria and eukaryotes except the vertebrates. It plays an important role in a number of critical metabolic functions especially in response to stressful environmental conditions. However, the biosynthetic pathways of trehalose in cold-adapted yeast and its responses to temperature and salinity changes remain little understood. In this study, the genome of Antarctic-isolated Pseudozyma sp. NJ7 was generated from which we identified the gene coding for trehalose phosphate synthase (TPS1) and trehalose phosphate phosphatase (TPS2), the two enzymes most critical for trehalose production. The whole draft genome length of Pseudozyma sp. NJ7 was 18,021,233 bp, and encoded at least 34 rRNA operons and 72 tRNAs. The open reading frame of tps1 contained 1827 nucleotide encoding 608 amino acids with a molecular weight of 67.64 kDa, and an isoelectric point of 5.54, while tps2 contained 3948 nucleotide encoding 1315 amino acids with a molecular weight of 144.47 kDa and an isoelectric point of 6.36. The TPS1 and TPS2 protein sequences were highly homologous to Moesziomyces antarcticus T-34, but TPS2 had obvious specificity and differently with others which suggest species specificity and different evolutionary history. Expression level of tps1 gene was strongly influenced by temperature and high salinity. In addition, addition of 0.5% trehalose preserved yeast cells in the short term but was not effective for cryopreservation for more than 5 days, but still suggesting that exogenous trehalose could indeed significantly improve the survival of yeast cells under freezing conditions. Our results provided new insights on the molecular basis of cold adaptations of Antarctic Pseudozyma sp., and also generated new information on the roles trehalose play in yeast tolerance to extreme conditions in the extreme Antarctic environments.
format Text
author Yin, Hua
Wang, Yibin
He, Yingying
Xing, Lei
Zhang, Xiufang
Wang, Shuai
Qi, Xiaoqing
Zheng, Zhou
Lu, Jian
Miao, Jinlai
author_facet Yin, Hua
Wang, Yibin
He, Yingying
Xing, Lei
Zhang, Xiufang
Wang, Shuai
Qi, Xiaoqing
Zheng, Zhou
Lu, Jian
Miao, Jinlai
author_sort Yin, Hua
title Cloning and expression analysis of tps, and cryopreservation research of trehalose from Antarctic strain Pseudozyma sp.
title_short Cloning and expression analysis of tps, and cryopreservation research of trehalose from Antarctic strain Pseudozyma sp.
title_full Cloning and expression analysis of tps, and cryopreservation research of trehalose from Antarctic strain Pseudozyma sp.
title_fullStr Cloning and expression analysis of tps, and cryopreservation research of trehalose from Antarctic strain Pseudozyma sp.
title_full_unstemmed Cloning and expression analysis of tps, and cryopreservation research of trehalose from Antarctic strain Pseudozyma sp.
title_sort cloning and expression analysis of tps, and cryopreservation research of trehalose from antarctic strain pseudozyma sp.
publisher Springer Berlin Heidelberg
publishDate 2017
url http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5610133/
http://www.ncbi.nlm.nih.gov/pubmed/28955640
https://doi.org/10.1007/s13205-017-0983-3
geographic Antarctic
geographic_facet Antarctic
genre Antarc*
Antarctic
antarcticus
genre_facet Antarc*
Antarctic
antarcticus
op_relation http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5610133/
http://www.ncbi.nlm.nih.gov/pubmed/28955640
http://dx.doi.org/10.1007/s13205-017-0983-3
op_rights © Springer-Verlag GmbH Germany 2017
op_doi https://doi.org/10.1007/s13205-017-0983-3
container_title 3 Biotech
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