Chenqi Xu, Han Peng, He Li, Xinran Xie, Siwei Chen, Junhao Dai, Hong Ren
{"title":"从猕猴桃树根瘤土壤中分离出的新型细菌 Paracoccus actinidiae sp.nov.","authors":"Chenqi Xu, Han Peng, He Li, Xinran Xie, Siwei Chen, Junhao Dai, Hong Ren","doi":"10.1099/ijsem.0.006529","DOIUrl":null,"url":null,"abstract":"<p><p>Strain M09<sup>T</sup> was isolated from the rhizoshere of kiwi fruit trees from an orchard located in Fangshan, Beijing, PR China (39° 49' 25.1″ N, 116° 4' 44.5″ E,). It is a short rod-shaped, Gram-stain-negative, facultatively anaerobic bacterium that tests positive for both oxidase and catalase. The strain exhibited growth within the temperature range of 15-45 °C (optimal growth at 30 °C) and the pH range of 4.0-10.0 (optimal growth at pH 7.0) and without NaCl. It also grew in a sodium chloride-free nutrient agar (NA) medium. The results of phylogenetic analysis of the 16S rRNA gene sequences indicated that M09<sup>T</sup> represents a member of the genus <i>Paracoccus</i> and shares high similarity with <i>Paracoccus everestensis</i> S8-55<sup>T</sup> (98.46%) and <i>Paracoccus aerius</i> 011410<sup>T</sup> (97.58%). The average nucleotide identity values between M09<sup>T</sup> and <i>P. everestensis</i> S8-55<sup>T</sup>, <i>P. aerius</i> 011410<sup>T</sup>, <i>Paracoccus marinaquae</i> X HP0099<sup>T</sup> and <i>Paracoccus fontiphilus</i> MVW-1<sup>T</sup> were 95.56, 84.51, 79.83 and 83.68%, respectively. The digital DNA-DNA hybridisation values between between M09<sup>T</sup> and <i>P. everestensis</i> S8-55<sup>T</sup>, <i>P. aerius</i> 011410<sup>T</sup>, <i>P. marinaquae</i> X HP0099<sup>T</sup> and <i>P. fontiphilus</i> MVW-1<sup>T</sup> were 56.40, 29.30, 21.60 and 28.60%, respectively. The major fatty acids identified were C<sub>10 : 0</sub> 3-OH (51.8%) and C<sub>18 : 1</sub>ω7<i>c</i> (35.5%). The major respiratory quinone was Q-10, with Q-8 present as a minor component. Polar lipids were mainly comprised of diphosphatidylglycerol (DPG), phosphatidylglycerol (PG), phosphatidylcholine (PC), and phosphatidylethanolamine (PE). Genome sequencing revealed that the strain has a DNA G+C content of 64.31 mol%. On the basis of this comprehensive taxonomic characterisation data, M09<sup>T</sup> represents a novel species within the genus <i>Paracoccus</i> and has been named <i>Paracoccus actinidiae</i> sp. nov. The type strain is designated as M09<sup>T</sup> (=GDMCC 1.4157<sup>T</sup>=KCTC 8143<sup>T</sup>).</p>","PeriodicalId":2,"journal":{"name":"ACS Applied Bio Materials","volume":null,"pages":null},"PeriodicalIF":4.6000,"publicationDate":"2024-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"<i>Paracoccus actinidiae</i> sp.nov., a novel bacterium isolated from kiwi tree rhizosphere soil.\",\"authors\":\"Chenqi Xu, Han Peng, He Li, Xinran Xie, Siwei Chen, Junhao Dai, Hong Ren\",\"doi\":\"10.1099/ijsem.0.006529\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Strain M09<sup>T</sup> was isolated from the rhizoshere of kiwi fruit trees from an orchard located in Fangshan, Beijing, PR China (39° 49' 25.1″ N, 116° 4' 44.5″ E,). It is a short rod-shaped, Gram-stain-negative, facultatively anaerobic bacterium that tests positive for both oxidase and catalase. The strain exhibited growth within the temperature range of 15-45 °C (optimal growth at 30 °C) and the pH range of 4.0-10.0 (optimal growth at pH 7.0) and without NaCl. It also grew in a sodium chloride-free nutrient agar (NA) medium. The results of phylogenetic analysis of the 16S rRNA gene sequences indicated that M09<sup>T</sup> represents a member of the genus <i>Paracoccus</i> and shares high similarity with <i>Paracoccus everestensis</i> S8-55<sup>T</sup> (98.46%) and <i>Paracoccus aerius</i> 011410<sup>T</sup> (97.58%). The average nucleotide identity values between M09<sup>T</sup> and <i>P. everestensis</i> S8-55<sup>T</sup>, <i>P. aerius</i> 011410<sup>T</sup>, <i>Paracoccus marinaquae</i> X HP0099<sup>T</sup> and <i>Paracoccus fontiphilus</i> MVW-1<sup>T</sup> were 95.56, 84.51, 79.83 and 83.68%, respectively. The digital DNA-DNA hybridisation values between between M09<sup>T</sup> and <i>P. everestensis</i> S8-55<sup>T</sup>, <i>P. aerius</i> 011410<sup>T</sup>, <i>P. marinaquae</i> X HP0099<sup>T</sup> and <i>P. fontiphilus</i> MVW-1<sup>T</sup> were 56.40, 29.30, 21.60 and 28.60%, respectively. The major fatty acids identified were C<sub>10 : 0</sub> 3-OH (51.8%) and C<sub>18 : 1</sub>ω7<i>c</i> (35.5%). The major respiratory quinone was Q-10, with Q-8 present as a minor component. Polar lipids were mainly comprised of diphosphatidylglycerol (DPG), phosphatidylglycerol (PG), phosphatidylcholine (PC), and phosphatidylethanolamine (PE). Genome sequencing revealed that the strain has a DNA G+C content of 64.31 mol%. On the basis of this comprehensive taxonomic characterisation data, M09<sup>T</sup> represents a novel species within the genus <i>Paracoccus</i> and has been named <i>Paracoccus actinidiae</i> sp. nov. The type strain is designated as M09<sup>T</sup> (=GDMCC 1.4157<sup>T</sup>=KCTC 8143<sup>T</sup>).</p>\",\"PeriodicalId\":2,\"journal\":{\"name\":\"ACS Applied Bio Materials\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":4.6000,\"publicationDate\":\"2024-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Applied Bio Materials\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1099/ijsem.0.006529\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"MATERIALS SCIENCE, BIOMATERIALS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Bio Materials","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1099/ijsem.0.006529","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MATERIALS SCIENCE, BIOMATERIALS","Score":null,"Total":0}
Paracoccus actinidiae sp.nov., a novel bacterium isolated from kiwi tree rhizosphere soil.
Strain M09T was isolated from the rhizoshere of kiwi fruit trees from an orchard located in Fangshan, Beijing, PR China (39° 49' 25.1″ N, 116° 4' 44.5″ E,). It is a short rod-shaped, Gram-stain-negative, facultatively anaerobic bacterium that tests positive for both oxidase and catalase. The strain exhibited growth within the temperature range of 15-45 °C (optimal growth at 30 °C) and the pH range of 4.0-10.0 (optimal growth at pH 7.0) and without NaCl. It also grew in a sodium chloride-free nutrient agar (NA) medium. The results of phylogenetic analysis of the 16S rRNA gene sequences indicated that M09T represents a member of the genus Paracoccus and shares high similarity with Paracoccus everestensis S8-55T (98.46%) and Paracoccus aerius 011410T (97.58%). The average nucleotide identity values between M09T and P. everestensis S8-55T, P. aerius 011410T, Paracoccus marinaquae X HP0099T and Paracoccus fontiphilus MVW-1T were 95.56, 84.51, 79.83 and 83.68%, respectively. The digital DNA-DNA hybridisation values between between M09T and P. everestensis S8-55T, P. aerius 011410T, P. marinaquae X HP0099T and P. fontiphilus MVW-1T were 56.40, 29.30, 21.60 and 28.60%, respectively. The major fatty acids identified were C10 : 0 3-OH (51.8%) and C18 : 1ω7c (35.5%). The major respiratory quinone was Q-10, with Q-8 present as a minor component. Polar lipids were mainly comprised of diphosphatidylglycerol (DPG), phosphatidylglycerol (PG), phosphatidylcholine (PC), and phosphatidylethanolamine (PE). Genome sequencing revealed that the strain has a DNA G+C content of 64.31 mol%. On the basis of this comprehensive taxonomic characterisation data, M09T represents a novel species within the genus Paracoccus and has been named Paracoccus actinidiae sp. nov. The type strain is designated as M09T (=GDMCC 1.4157T=KCTC 8143T).