Chemical characterization, pathway enrichments and bioactive potentials of catechin-producing endophytic fungi isolated from tea leaves

Endophytes acquire flavonoid biosynthetic genes from the host medicinal plants. Despite tea ( (L.) Kuntze) being the major source of bioactive catechins, catechin-producing endophytic fungi have never been reported from the tea plant. Here, we report the isolation and characterization of catechin-pr...

Full description

Saved in:
Bibliographic Details
Published in:RSC advances Vol. 14; no. 45; pp. 33034 - 33047
Main Authors: Sidhu, Dwinder, Vasundhara, M, Dey, Priyankar
Format: Journal Article
Language:English
Published: England Royal Society of Chemistry 17-10-2024
The Royal Society of Chemistry
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Abstract Endophytes acquire flavonoid biosynthetic genes from the host medicinal plants. Despite tea ( (L.) Kuntze) being the major source of bioactive catechins, catechin-producing endophytic fungi have never been reported from the tea plant. Here, we report the isolation and characterization of catechin-producing endophytic fungi isolated from tea leaves, their chemical characterization, and associated bioactivities. Among the nine isolated endophytes, two (CSPL6 and CSPL5b) produced catechin (381.48 and 166.40 μg per mg extract) and epigallocatechin- -gallate (EGCG; 484.41 and 281.99 μg per mg extract) as quantified by high-performance liquid chromatography (HPLC). The isolates were identified as and based on molecular and morphological characterization. Untargeted metabolomics using gas-chromatography mass spectroscopy (GCMS) revealed the presence of several bioactive phytochemicals mostly belonging to tyrosols, pyridoxines, fatty acids, aminopyrimidine, and benzenetriol classes. Metabolic pathways pertaining to the biosynthesis of unsaturated fatty acids (UFAs), butanoate metabolism, and linoleic acid metabolism were highly enriched in both catechin-producing isolates. The isolates were able to differentially scavenge intracellular O and N free-radicals, but CSPL5b demonstrated relatively superior bioactivities compared to CSPL6. Both isolates stimulated the growth of various probiotic strains, indicating prebiotic effects that are otherwise known to be associated with catechins. Collectively, the current study demonstrated that fungal endophytes CSPL6 and CSPL5b, isolated from tea leaves, could be used as alternative sources of catechins, and hold promising potential in evidence-based therapeutics.
AbstractList Endophytes acquire flavonoid biosynthetic genes from the host medicinal plants. Despite tea (Camellia sinensis (L.) Kuntze) being the major source of bioactive catechins, catechin-producing endophytic fungi have never been reported from the tea plant. Here, we report the isolation and characterization of catechin-producing endophytic fungi isolated from tea leaves, their chemical characterization, and associated bioactivities. Among the nine isolated endophytes, two (CSPL6 and CSPL5b) produced catechin (381.48 and 166.40 μg per mg extract) and epigallocatechin-o-gallate (EGCG; 484.41 and 281.99 μg per mg extract) as quantified by high-performance liquid chromatography (HPLC). The isolates were identified as Pseudopestalotiopsis camelliae-sinensis and Didymella sinensis based on molecular and morphological characterization. Untargeted metabolomics using gas-chromatography mass spectroscopy (GCMS) revealed the presence of several bioactive phytochemicals mostly belonging to tyrosols, pyridoxines, fatty acids, aminopyrimidine, and benzenetriol classes. Metabolic pathways pertaining to the biosynthesis of unsaturated fatty acids (UFAs), butanoate metabolism, and linoleic acid metabolism were highly enriched in both catechin-producing isolates. The isolates were able to differentially scavenge intracellular O2 and N2 free-radicals, but CSPL5b demonstrated relatively superior bioactivities compared to CSPL6. Both isolates stimulated the growth of various probiotic strains, indicating prebiotic effects that are otherwise known to be associated with catechins. Collectively, the current study demonstrated that fungal endophytes CSPL6 and CSPL5b, isolated from tea leaves, could be used as alternative sources of catechins, and hold promising potential in evidence-based therapeutics.
Endophytes acquire flavonoid biosynthetic genes from the host medicinal plants. Despite tea (Camellia sinensis (L.) Kuntze) being the major source of bioactive catechins, catechin-producing endophytic fungi have never been reported from the tea plant. Here, we report the isolation and characterization of catechin-producing endophytic fungi isolated from tea leaves, their chemical characterization, and associated bioactivities. Among the nine isolated endophytes, two (CSPL6 and CSPL5b) produced catechin (381.48 and 166.40 μg per mg extract) and epigallocatechin-o-gallate (EGCG; 484.41 and 281.99 μg per mg extract) as quantified by high-performance liquid chromatography (HPLC). The isolates were identified as Pseudopestalotiopsis camelliae-sinensis and Didymella sinensis based on molecular and morphological characterization. Untargeted metabolomics using gas-chromatography mass spectroscopy (GCMS) revealed the presence of several bioactive phytochemicals mostly belonging to tyrosols, pyridoxines, fatty acids, aminopyrimidine, and benzenetriol classes. Metabolic pathways pertaining to the biosynthesis of unsaturated fatty acids (UFAs), butanoate metabolism, and linoleic acid metabolism were highly enriched in both catechin-producing isolates. The isolates were able to differentially scavenge intracellular O2 and N2 free-radicals, but CSPL5b demonstrated relatively superior bioactivities compared to CSPL6. Both isolates stimulated the growth of various probiotic strains, indicating prebiotic effects that are otherwise known to be associated with catechins. Collectively, the current study demonstrated that fungal endophytes CSPL6 and CSPL5b, isolated from tea leaves, could be used as alternative sources of catechins, and hold promising potential in evidence-based therapeutics.Endophytes acquire flavonoid biosynthetic genes from the host medicinal plants. Despite tea (Camellia sinensis (L.) Kuntze) being the major source of bioactive catechins, catechin-producing endophytic fungi have never been reported from the tea plant. Here, we report the isolation and characterization of catechin-producing endophytic fungi isolated from tea leaves, their chemical characterization, and associated bioactivities. Among the nine isolated endophytes, two (CSPL6 and CSPL5b) produced catechin (381.48 and 166.40 μg per mg extract) and epigallocatechin-o-gallate (EGCG; 484.41 and 281.99 μg per mg extract) as quantified by high-performance liquid chromatography (HPLC). The isolates were identified as Pseudopestalotiopsis camelliae-sinensis and Didymella sinensis based on molecular and morphological characterization. Untargeted metabolomics using gas-chromatography mass spectroscopy (GCMS) revealed the presence of several bioactive phytochemicals mostly belonging to tyrosols, pyridoxines, fatty acids, aminopyrimidine, and benzenetriol classes. Metabolic pathways pertaining to the biosynthesis of unsaturated fatty acids (UFAs), butanoate metabolism, and linoleic acid metabolism were highly enriched in both catechin-producing isolates. The isolates were able to differentially scavenge intracellular O2 and N2 free-radicals, but CSPL5b demonstrated relatively superior bioactivities compared to CSPL6. Both isolates stimulated the growth of various probiotic strains, indicating prebiotic effects that are otherwise known to be associated with catechins. Collectively, the current study demonstrated that fungal endophytes CSPL6 and CSPL5b, isolated from tea leaves, could be used as alternative sources of catechins, and hold promising potential in evidence-based therapeutics.
Endophytes acquire flavonoid biosynthetic genes from the host medicinal plants. Despite tea ( Camellia sinensis (L.) Kuntze) being the major source of bioactive catechins, catechin-producing endophytic fungi have never been reported from the tea plant. Here, we report the isolation and characterization of catechin-producing endophytic fungi isolated from tea leaves, their chemical characterization, and associated bioactivities. Among the nine isolated endophytes, two (CSPL6 and CSPL5b) produced catechin (381.48 and 166.40 μg per mg extract) and epigallocatechin- o -gallate (EGCG; 484.41 and 281.99 μg per mg extract) as quantified by high-performance liquid chromatography (HPLC). The isolates were identified as Pseudopestalotiopsis camelliae-sinensis and Didymella sinensis based on molecular and morphological characterization. Untargeted metabolomics using gas-chromatography mass spectroscopy (GCMS) revealed the presence of several bioactive phytochemicals mostly belonging to tyrosols, pyridoxines, fatty acids, aminopyrimidine, and benzenetriol classes. Metabolic pathways pertaining to the biosynthesis of unsaturated fatty acids (UFAs), butanoate metabolism, and linoleic acid metabolism were highly enriched in both catechin-producing isolates. The isolates were able to differentially scavenge intracellular O 2 and N 2 free-radicals, but CSPL5b demonstrated relatively superior bioactivities compared to CSPL6. Both isolates stimulated the growth of various probiotic strains, indicating prebiotic effects that are otherwise known to be associated with catechins. Collectively, the current study demonstrated that fungal endophytes CSPL6 and CSPL5b, isolated from tea leaves, could be used as alternative sources of catechins, and hold promising potential in evidence-based therapeutics. Endophytes acquire flavonoid biosynthetic genes from the host medicinal plants.
Endophytes acquire flavonoid biosynthetic genes from the host medicinal plants. Despite tea ( (L.) Kuntze) being the major source of bioactive catechins, catechin-producing endophytic fungi have never been reported from the tea plant. Here, we report the isolation and characterization of catechin-producing endophytic fungi isolated from tea leaves, their chemical characterization, and associated bioactivities. Among the nine isolated endophytes, two (CSPL6 and CSPL5b) produced catechin (381.48 and 166.40 μg per mg extract) and epigallocatechin- -gallate (EGCG; 484.41 and 281.99 μg per mg extract) as quantified by high-performance liquid chromatography (HPLC). The isolates were identified as and based on molecular and morphological characterization. Untargeted metabolomics using gas-chromatography mass spectroscopy (GCMS) revealed the presence of several bioactive phytochemicals mostly belonging to tyrosols, pyridoxines, fatty acids, aminopyrimidine, and benzenetriol classes. Metabolic pathways pertaining to the biosynthesis of unsaturated fatty acids (UFAs), butanoate metabolism, and linoleic acid metabolism were highly enriched in both catechin-producing isolates. The isolates were able to differentially scavenge intracellular O and N free-radicals, but CSPL5b demonstrated relatively superior bioactivities compared to CSPL6. Both isolates stimulated the growth of various probiotic strains, indicating prebiotic effects that are otherwise known to be associated with catechins. Collectively, the current study demonstrated that fungal endophytes CSPL6 and CSPL5b, isolated from tea leaves, could be used as alternative sources of catechins, and hold promising potential in evidence-based therapeutics.
Endophytes acquire flavonoid biosynthetic genes from the host medicinal plants. Despite tea ( Camellia sinensis (L.) Kuntze) being the major source of bioactive catechins, catechin-producing endophytic fungi have never been reported from the tea plant. Here, we report the isolation and characterization of catechin-producing endophytic fungi isolated from tea leaves, their chemical characterization, and associated bioactivities. Among the nine isolated endophytes, two (CSPL6 and CSPL5b) produced catechin (381.48 and 166.40 μg per mg extract) and epigallocatechin- o -gallate (EGCG; 484.41 and 281.99 μg per mg extract) as quantified by high-performance liquid chromatography (HPLC). The isolates were identified as Pseudopestalotiopsis camelliae-sinensis and Didymella sinensis based on molecular and morphological characterization. Untargeted metabolomics using gas-chromatography mass spectroscopy (GCMS) revealed the presence of several bioactive phytochemicals mostly belonging to tyrosols, pyridoxines, fatty acids, aminopyrimidine, and benzenetriol classes. Metabolic pathways pertaining to the biosynthesis of unsaturated fatty acids (UFAs), butanoate metabolism, and linoleic acid metabolism were highly enriched in both catechin-producing isolates. The isolates were able to differentially scavenge intracellular O 2 and N 2 free-radicals, but CSPL5b demonstrated relatively superior bioactivities compared to CSPL6. Both isolates stimulated the growth of various probiotic strains, indicating prebiotic effects that are otherwise known to be associated with catechins. Collectively, the current study demonstrated that fungal endophytes CSPL6 and CSPL5b, isolated from tea leaves, could be used as alternative sources of catechins, and hold promising potential in evidence-based therapeutics.
Author Vasundhara, M
Sidhu, Dwinder
Dey, Priyankar
Author_xml – sequence: 1
  givenname: Dwinder
  surname: Sidhu
  fullname: Sidhu, Dwinder
  email: priyankar.dey@thapar.edu, mvasundhara@thapar.edu
  organization: Department of Biotechnology, Thapar Institute of Engineering & Technology Patiala Punjab 147004 India priyankar.dey@thapar.edu mvasundhara@thapar.edu +91-9064275660 +91-8146480908
– sequence: 2
  givenname: M
  surname: Vasundhara
  fullname: Vasundhara, M
  email: priyankar.dey@thapar.edu, mvasundhara@thapar.edu
  organization: Department of Biotechnology, Thapar Institute of Engineering & Technology Patiala Punjab 147004 India priyankar.dey@thapar.edu mvasundhara@thapar.edu +91-9064275660 +91-8146480908
– sequence: 3
  givenname: Priyankar
  orcidid: 0000-0002-9513-425X
  surname: Dey
  fullname: Dey, Priyankar
  email: priyankar.dey@thapar.edu, mvasundhara@thapar.edu
  organization: Department of Biotechnology, Thapar Institute of Engineering & Technology Patiala Punjab 147004 India priyankar.dey@thapar.edu mvasundhara@thapar.edu +91-9064275660 +91-8146480908
BackLink https://www.ncbi.nlm.nih.gov/pubmed/39434990$$D View this record in MEDLINE/PubMed
BookMark eNpdkd1u1DAQhS1URMvSGx4AWeIGIRb8F2d9Va2WX6kSEoLraOJMNq4SO9jOouUFeG1cWqrC3Hg0_nx0xucxOfHBIyFPOXvNmTRvOhWBVXW1gQfkTDCl14Jpc3KvPyXnKV2xUrriQvNH5FQaJZUx7Iz82g04OQsjtQNEsBmj-wnZBf-KzpCHH3Ck6KOzw4Q-Jwq-o60LBXQHpHPIZepgTDT01EJGOzi_nmPoFuv8vjztwjwcs7O0X_zeUZfCWLCO9jFMNCPQEeGA6Ql52BcZPL89V-Tb-3dfdx_Xl58_fNptL9dWaJbXdW9YxXllKsYQoG57JqWtDIhWAGotUBtAkErIqtvY1qiuBYHdZqOZqCuQK3Jxozsv7YSdLfYjjM0c3QTx2ARwzb833g3NPhwazpURvPzbiry4VYjh-4IpN5NLFscRPIYlNZJzw42sxTX6_D_0KizRl_0KJZTSxtSyUC9vKBtDShH7OzecNdcZN2_Vl-2fjLcFfnbf_x36N1H5G7KZpus
Cites_doi 10.1016/0006-2952(88)90169-4
10.3390/ijms231810735
10.1186/s12870-020-02777-7
10.1186/s12866-019-1672-7
10.1021/acs.jafc.9b03946
10.1038/s41598-020-75722-1
10.1094/PDIS-05-20-0939-A
10.1016/j.foodres.2012.10.014
10.1016/j.jnutbio.2019.01.017
10.3897/mycokeys.105.119536
10.1155/2014/360438
10.1016/j.jnutbio.2022.109094
10.3390/app11114905
10.1002/eap.1607
10.3390/molecules27030771
10.1007/s10661-021-08937-y
10.1007/s12298-020-00836-9
10.3389/fpls.2022.989794
10.3389/fpls.2020.594317
10.5943/mycosphere/12/1/6
10.1016/j.jff.2017.10.015
10.1016/j.foodchem.2005.06.040
10.1371/journal.pone.0150574
10.1007/s42965-023-00304-x
10.1007/s10600-015-1205-z
10.1038/s41598-023-31291-7
10.1111/jam.15174
10.1007/s11274-019-2651-8
10.7717/peerj.8978
10.1016/j.ecoinf.2021.101546
10.3389/fmicb.2021.716523
10.1099/13500872-142-2-435
10.5897/AJMR12.2352
10.3389/fpls.2021.791033
10.1002/mnfr.200700086
10.1002/nt.2620010306
10.1111/pbi.12933
10.1016/S0014-5793(00)02234-1
10.1016/j.phymed.2023.155207
10.1016/0378-5173(90)90201-E
10.3389/fmicb.2022.872034
10.3389/fpls.2022.896421
10.3109/08923973.2013.775588
10.5056/jnm.2014.20.2.265
10.1038/s41467-019-08515-4
10.3390/ijms24032739
10.1038/s41598-022-05820-9
10.1038/s41598-019-38837-8
10.1006/bbrc.1999.1263
10.1080/07388551.2020.1869691
10.1016/j.heliyon.2023.e21392
10.1042/bj2480973
10.1038/s41598-023-47260-z
10.1128/AEM.00753-08
10.3390/molecules26196052
10.3390/molecules26030654
10.1016/j.jgeb.2015.12.003
10.15666/aeer/1601_677695
10.1007/s40828-019-0101-8
10.1371/journal.pone.0109126
10.1007/s00394-018-01890-6
10.1016/j.jnutbio.2020.108455
10.1007/s10600-013-0658-1
10.3389/fpls.2020.00390
10.1080/21655979.2020.1816788
10.1093/nar/gks374
10.1016/j.fitote.2014.09.015
10.1038/s41438-021-00538-7
10.3390/cli5030046
10.1155/2014/792789
10.3390/jof9121191
10.1080/13813455.2021.1966475
10.3389/fpls.2020.562785
10.32604/phyton.2014.83.057
10.1038/s41598-017-00972-5
10.1038/s41598-023-47657-w
10.1007/s13213-010-0016-5
10.1016/j.foodhyd.2024.109768
10.3390/antiox12040930
10.3390/stresses2030019
10.1007/s13205-022-03145-y
10.1038/nprot.2006.384
10.1111/j.1745-4581.2009.00187.x
ContentType Journal Article
Copyright This journal is © The Royal Society of Chemistry.
Copyright Royal Society of Chemistry 2024
This journal is © The Royal Society of Chemistry 2024 The Royal Society of Chemistry
Copyright_xml – notice: This journal is © The Royal Society of Chemistry.
– notice: Copyright Royal Society of Chemistry 2024
– notice: This journal is © The Royal Society of Chemistry 2024 The Royal Society of Chemistry
DBID NPM
AAYXX
CITATION
7SR
8BQ
8FD
JG9
7X8
5PM
DOI 10.1039/d4ra05758a
DatabaseName PubMed
CrossRef
Engineered Materials Abstracts
METADEX
Technology Research Database
Materials Research Database
MEDLINE - Academic
PubMed Central (Full Participant titles)
DatabaseTitle PubMed
CrossRef
Materials Research Database
Engineered Materials Abstracts
Technology Research Database
METADEX
MEDLINE - Academic
DatabaseTitleList Materials Research Database
MEDLINE - Academic

PubMed
CrossRef
DeliveryMethod fulltext_linktorsrc
Discipline Chemistry
EISSN 2046-2069
EndPage 33047
ExternalDocumentID 10_1039_D4RA05758A
39434990
Genre Journal Article
GrantInformation_xml – fundername: ;
  grantid: SPG/2021/003324
GroupedDBID -JG
0-7
0R~
53G
AAFWJ
AAHBH
AAIWI
AAJAE
AARTK
AAWGC
AAXHV
ABEMK
ABGFH
ABPDG
ABXOH
ACGFS
ADBBV
ADMRA
AEFDR
AENEX
AESAV
AFLYV
AFVBQ
AGEGJ
AGRSR
AGSTE
AHGCF
AKBGW
ALMA_UNASSIGNED_HOLDINGS
ANUXI
APEMP
ASKNT
AUDPV
BCNDV
BLAPV
BSQNT
C6K
EBS
EE0
EF-
GROUPED_DOAJ
H13
HZ~
H~N
J3I
M~E
NPM
O9-
OK1
PGMZT
R7C
R7G
RCNCU
RPM
RPMJG
RRC
RSCEA
RVUXY
SLH
SMJ
ZCN
AAYXX
CITATION
7SR
8BQ
8FD
JG9
7X8
5PM
ID FETCH-LOGICAL-c260t-7f9051159500eaa7bf033c59a2b2ae662e69aea34235d8cb94dba2ed8860275a3
IEDL.DBID RPM
ISSN 2046-2069
IngestDate Tue Oct 22 05:20:53 EDT 2024
Thu Oct 24 02:27:41 EDT 2024
Wed Nov 06 12:25:27 EST 2024
Wed Oct 23 14:16:42 EDT 2024
Sat Nov 02 11:58:30 EDT 2024
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 45
Language English
License This journal is © The Royal Society of Chemistry.
This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c260t-7f9051159500eaa7bf033c59a2b2ae662e69aea34235d8cb94dba2ed8860275a3
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ORCID 0000-0002-9513-425X
OpenAccessLink https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11492194/
PMID 39434990
PQID 3124469973
PQPubID 2047525
PageCount 14
ParticipantIDs pubmedcentral_primary_oai_pubmedcentral_nih_gov_11492194
proquest_miscellaneous_3119193724
proquest_journals_3124469973
crossref_primary_10_1039_D4RA05758A
pubmed_primary_39434990
PublicationCentury 2000
PublicationDate 2024-10-17
PublicationDateYYYYMMDD 2024-10-17
PublicationDate_xml – month: 10
  year: 2024
  text: 2024-10-17
  day: 17
PublicationDecade 2020
PublicationPlace England
PublicationPlace_xml – name: England
– name: Cambridge
PublicationTitle RSC advances
PublicationTitleAlternate RSC Adv
PublicationYear 2024
Publisher Royal Society of Chemistry
The Royal Society of Chemistry
Publisher_xml – name: Royal Society of Chemistry
– name: The Royal Society of Chemistry
References Walter (D4RA05758A/cit92/1) 2008; 74
Pharamat (D4RA05758A/cit31/1) 2013; 7
Wangkarn (D4RA05758A/cit37/1) 2021; 26
Dey (D4RA05758A/cit35/1) 2020; 84
Aruoma (D4RA05758A/cit51/1) 1987; 248
Sun (D4RA05758A/cit70/1) 2019; 67
Sun (D4RA05758A/cit90/1) 2022; 109
Bhadra (D4RA05758A/cit2/1) 2022; 12
Green (D4RA05758A/cit38/1) 2007; 51
Xie (D4RA05758A/cit68/1) 2020; 11
He (D4RA05758A/cit76/1) 2020; 11
Marx (D4RA05758A/cit8/1) 2017; 5
Long (D4RA05758A/cit46/1) 1999; 262
Dutta (D4RA05758A/cit47/1) 2017; 39
Garratt (D4RA05758A/cit49/1) 2012
Manawasinghe (D4RA05758A/cit24/1) 2021; 12
Shahriar (D4RA05758A/cit58/1) 2022
Deng (D4RA05758A/cit82/1) 2019; 9
Haro-Vicente (D4RA05758A/cit48/1) 2006; 98
Hazarika (D4RA05758A/cit15/1) 2022; 13
Cerbin-Koczorowska (D4RA05758A/cit7/1) 2021; 11
Azuddin (D4RA05758A/cit20/1) 2023; 13
Murotomi (D4RA05758A/cit89/1) 2023; 24
Rezgui (D4RA05758A/cit39/1) 2023; 12
Manish (D4RA05758A/cit3/1) 2022; 68
Petrini (D4RA05758A/cit22/1) 1993; 1
Dey (D4RA05758A/cit45/1) 2012; 4
Rabha (D4RA05758A/cit27/1) 2016; 14
Onlamun (D4RA05758A/cit13/1) 2023; 9
Andrés (D4RA05758A/cit87/1) 2022; 2
Xj (D4RA05758A/cit62/1) 2014; 83
Lee (D4RA05758A/cit91/1) 2014; 20
Rohr (D4RA05758A/cit56/1) 2017; 27
Liu (D4RA05758A/cit57/1) 2017; 7
Wang (D4RA05758A/cit60/1) 2024; 105
Delatte (D4RA05758A/cit74/1) 2018; 16
Winterbourn (D4RA05758A/cit86/1) 2020; 6
Kaur (D4RA05758A/cit19/1) 2020; 10
Sadre (D4RA05758A/cit75/1) 2019; 10
Han (D4RA05758A/cit10/1) 2020; 11
Andrés (D4RA05758A/cit88/1) 2022; 23
Vasundhara (D4RA05758A/cit1/1) 2019
Xia (D4RA05758A/cit41/1) 2012; 40
Qiu (D4RA05758A/cit33/1) 2010; 60
Dey (D4RA05758A/cit36/1) 2019; 67
Xie (D4RA05758A/cit94/1) 2024; 151
Wang (D4RA05758A/cit65/1) 2014; 99
He (D4RA05758A/cit72/1) 2020; 11
Lin (D4RA05758A/cit81/1) 2021; 21
Vig (D4RA05758A/cit32/1) 2022; 132
Mani (D4RA05758A/cit18/1) 2021; 26
Sharma (D4RA05758A/cit93/1) 2019; 58
Nath (D4RA05758A/cit14/1) 2015; 13
Lin (D4RA05758A/cit53/1) 2022; 13
Roy (D4RA05758A/cit43/1) 2013; 35
Kunwar (D4RA05758A/cit4/1) 2014; 2014
Allen (D4RA05758A/cit26/1) 2006; 1
Prabavathy (D4RA05758A/cit30/1) 2011; 4
Saha (D4RA05758A/cit64/1) 2024; 130
Cheng (D4RA05758A/cit16/1) 2015; 51
Sidhu (D4RA05758A/cit5/1) 2024; 123
Charria-Girón (D4RA05758A/cit29/1) 2021; 12
Zi (D4RA05758A/cit79/1) 2022; 27
Alam (D4RA05758A/cit69/1) 2021; 12
Yao (D4RA05758A/cit71/1) 2021; 41
Kaur (D4RA05758A/cit67/1) 2020; 10
Tang (D4RA05758A/cit66/1) 2020; 8
Parida (D4RA05758A/cit9/1) 2023
Baruah (D4RA05758A/cit11/1) 2021; 193
Chen (D4RA05758A/cit77/1) 2022; 13
Qi (D4RA05758A/cit83/1) 2023; 13
Wu (D4RA05758A/cit54/1) 2020; 20
Habisukan (D4RA05758A/cit21/1) 2021; 22
Saha (D4RA05758A/cit42/1) 2016; 11
Ayala (D4RA05758A/cit85/1) 2014; 2014
Sultanbawa (D4RA05758A/cit52/1) 2009; 17
Win (D4RA05758A/cit55/1) 2018; 16
Gandhi (D4RA05758A/cit40/1) 2023; 9
Bailly (D4RA05758A/cit50/1) 2000; 486
Han (D4RA05758A/cit78/1) 2023; 13
Dey (D4RA05758A/cit6/1) 2023
Robak (D4RA05758A/cit84/1) 1988; 37
Cheng (D4RA05758A/cit17/1) 2013; 49
Gill (D4RA05758A/cit28/1) 2019; 35
Gaudreau (D4RA05758A/cit95/1) 2013; 53
Ratul (D4RA05758A/cit63/1) 2023; 18
Ahmed (D4RA05758A/cit12/1) 2014; 9
Kunchandy (D4RA05758A/cit44/1) 1990; 58
Yu (D4RA05758A/cit61/1) 2021; 8
Strobel (D4RA05758A/cit23/1) 1996; 142
Saffaryazdi (D4RA05758A/cit80/1) 2020; 26
Wani (D4RA05758A/cit34/1) 2018; 7
Wang (D4RA05758A/cit59/1) 2021; 105
Schultz (D4RA05758A/cit73/1) 2002
Ezeonuegbu (D4RA05758A/cit25/1) 2022; 12
References_xml – volume: 37
  start-page: 837
  year: 1988
  ident: D4RA05758A/cit84/1
  publication-title: Biochem. Pharmacol.
  doi: 10.1016/0006-2952(88)90169-4
  contributor:
    fullname: Robak
– volume: 7
  start-page: 2632
  year: 2018
  ident: D4RA05758A/cit34/1
  publication-title: Int. J. Adv. Res. Sci. Eng.
  contributor:
    fullname: Wani
– volume: 23
  start-page: 10735
  year: 2022
  ident: D4RA05758A/cit88/1
  publication-title: Int. J. Mol. Sci.
  doi: 10.3390/ijms231810735
  contributor:
    fullname: Andrés
– volume: 21
  start-page: 1
  year: 2021
  ident: D4RA05758A/cit81/1
  publication-title: BMC Plant Biol.
  doi: 10.1186/s12870-020-02777-7
  contributor:
    fullname: Lin
– volume: 20
  start-page: 1
  year: 2020
  ident: D4RA05758A/cit54/1
  publication-title: BMC Microbiol.
  doi: 10.1186/s12866-019-1672-7
  contributor:
    fullname: Wu
– volume: 67
  start-page: 10685
  year: 2019
  ident: D4RA05758A/cit70/1
  publication-title: J. Agric. Food Chem.
  doi: 10.1021/acs.jafc.9b03946
  contributor:
    fullname: Sun
– volume: 10
  start-page: 18792
  year: 2020
  ident: D4RA05758A/cit67/1
  publication-title: Sci. Rep.
  doi: 10.1038/s41598-020-75722-1
  contributor:
    fullname: Kaur
– start-page: 1
  year: 2022
  ident: D4RA05758A/cit58/1
  publication-title: Eur. J. Plant Pathol.
  contributor:
    fullname: Shahriar
– volume: 105
  start-page: 1168
  year: 2021
  ident: D4RA05758A/cit59/1
  publication-title: Plant Dis.
  doi: 10.1094/PDIS-05-20-0939-A
  contributor:
    fullname: Wang
– volume: 4
  start-page: 34
  year: 2011
  ident: D4RA05758A/cit30/1
  publication-title: J. Pharm. Res.
  contributor:
    fullname: Prabavathy
– volume: 53
  start-page: 751
  year: 2013
  ident: D4RA05758A/cit95/1
  publication-title: Food Res. Int.
  doi: 10.1016/j.foodres.2012.10.014
  contributor:
    fullname: Gaudreau
– volume: 22
  start-page: 1129
  issue: 3
  year: 2021
  ident: D4RA05758A/cit21/1
  publication-title: Biodiversitas: Journal of Biological Diversity
  contributor:
    fullname: Habisukan
– volume: 67
  start-page: 78
  year: 2019
  ident: D4RA05758A/cit36/1
  publication-title: J. Nutr. Biochem.
  doi: 10.1016/j.jnutbio.2019.01.017
  contributor:
    fullname: Dey
– start-page: 80
  volume-title: Food Chemistry, Function and Analysis
  year: 2023
  ident: D4RA05758A/cit6/1
  contributor:
    fullname: Dey
– volume: 105
  start-page: 217
  year: 2024
  ident: D4RA05758A/cit60/1
  publication-title: MycoKeys
  doi: 10.3897/mycokeys.105.119536
  contributor:
    fullname: Wang
– volume: 2014
  start-page: 360438
  year: 2014
  ident: D4RA05758A/cit85/1
  publication-title: Oxid. Med. Cell. Longevity
  doi: 10.1155/2014/360438
  contributor:
    fullname: Ayala
– volume: 109
  start-page: 109094
  year: 2022
  ident: D4RA05758A/cit90/1
  publication-title: J. Nutr. Biochem.
  doi: 10.1016/j.jnutbio.2022.109094
  contributor:
    fullname: Sun
– volume: 11
  start-page: 4905
  year: 2021
  ident: D4RA05758A/cit7/1
  publication-title: Appl. Sci.
  doi: 10.3390/app11114905
  contributor:
    fullname: Cerbin-Koczorowska
– volume: 27
  start-page: 2290
  year: 2017
  ident: D4RA05758A/cit56/1
  publication-title: Ecol. Appl.
  doi: 10.1002/eap.1607
  contributor:
    fullname: Rohr
– volume: 27
  start-page: 771
  year: 2022
  ident: D4RA05758A/cit79/1
  publication-title: Molecules
  doi: 10.3390/molecules27030771
  contributor:
    fullname: Zi
– volume: 4
  start-page: 54
  year: 2012
  ident: D4RA05758A/cit45/1
  publication-title: Int. J. Phytomed.
  contributor:
    fullname: Dey
– volume: 193
  start-page: 165
  year: 2021
  ident: D4RA05758A/cit11/1
  publication-title: Environ. Monit. Assess.
  doi: 10.1007/s10661-021-08937-y
  contributor:
    fullname: Baruah
– volume: 26
  start-page: 1519
  year: 2020
  ident: D4RA05758A/cit80/1
  publication-title: Physiol. Mol. Biol. Plants
  doi: 10.1007/s12298-020-00836-9
  contributor:
    fullname: Saffaryazdi
– volume: 13
  start-page: 989794
  year: 2022
  ident: D4RA05758A/cit15/1
  publication-title: Front. Plant Sci.
  doi: 10.3389/fpls.2022.989794
  contributor:
    fullname: Hazarika
– volume: 11
  start-page: 594317
  year: 2020
  ident: D4RA05758A/cit10/1
  publication-title: Front. Plant Sci.
  doi: 10.3389/fpls.2020.594317
  contributor:
    fullname: Han
– volume: 12
  start-page: 430
  issue: 1
  year: 2021
  ident: D4RA05758A/cit24/1
  publication-title: Mycosphere
  doi: 10.5943/mycosphere/12/1/6
  contributor:
    fullname: Manawasinghe
– volume: 39
  start-page: 112
  year: 2017
  ident: D4RA05758A/cit47/1
  publication-title: J. Funct. Foods
  doi: 10.1016/j.jff.2017.10.015
  contributor:
    fullname: Dutta
– volume: 98
  start-page: 639
  year: 2006
  ident: D4RA05758A/cit48/1
  publication-title: Food Chem.
  doi: 10.1016/j.foodchem.2005.06.040
  contributor:
    fullname: Haro-Vicente
– volume: 11
  start-page: e0150574
  year: 2016
  ident: D4RA05758A/cit42/1
  publication-title: PLoS One
  doi: 10.1371/journal.pone.0150574
  contributor:
    fullname: Saha
– start-page: 1
  year: 2023
  ident: D4RA05758A/cit9/1
  publication-title: Trop. Ecol.
  doi: 10.1007/s42965-023-00304-x
  contributor:
    fullname: Parida
– volume: 51
  start-page: 67
  year: 2015
  ident: D4RA05758A/cit16/1
  publication-title: Chem. Nat. Compd.
  doi: 10.1007/s10600-015-1205-z
  contributor:
    fullname: Cheng
– volume: 13
  start-page: 4239
  year: 2023
  ident: D4RA05758A/cit20/1
  publication-title: Sci. Rep.
  doi: 10.1038/s41598-023-31291-7
  contributor:
    fullname: Azuddin
– volume: 132
  start-page: 365
  year: 2022
  ident: D4RA05758A/cit32/1
  publication-title: J. Appl. Microbiol.
  doi: 10.1111/jam.15174
  contributor:
    fullname: Vig
– volume: 35
  start-page: 1
  year: 2019
  ident: D4RA05758A/cit28/1
  publication-title: World J. Microbiol. Biotechnol.
  doi: 10.1007/s11274-019-2651-8
  contributor:
    fullname: Gill
– volume: 8
  start-page: e8978
  year: 2020
  ident: D4RA05758A/cit66/1
  publication-title: PeerJ
  doi: 10.7717/peerj.8978
  contributor:
    fullname: Tang
– volume: 68
  start-page: 101546
  year: 2022
  ident: D4RA05758A/cit3/1
  publication-title: Ecol. Inf.
  doi: 10.1016/j.ecoinf.2021.101546
  contributor:
    fullname: Manish
– volume: 12
  start-page: 2515
  year: 2021
  ident: D4RA05758A/cit29/1
  publication-title: Front. Microbiol.
  doi: 10.3389/fmicb.2021.716523
  contributor:
    fullname: Charria-Girón
– volume: 142
  start-page: 435
  year: 1996
  ident: D4RA05758A/cit23/1
  publication-title: Microbiology
  doi: 10.1099/13500872-142-2-435
  contributor:
    fullname: Strobel
– volume: 7
  start-page: 5565
  year: 2013
  ident: D4RA05758A/cit31/1
  publication-title: Afr. J. Microbiol. Res.
  doi: 10.5897/AJMR12.2352
  contributor:
    fullname: Pharamat
– volume: 12
  start-page: 791033
  year: 2021
  ident: D4RA05758A/cit69/1
  publication-title: Front. Plant Sci.
  doi: 10.3389/fpls.2021.791033
  contributor:
    fullname: Alam
– volume: 51
  start-page: 1152
  year: 2007
  ident: D4RA05758A/cit38/1
  publication-title: Mol. Nutr. Food Res.
  doi: 10.1002/mnfr.200700086
  contributor:
    fullname: Green
– volume: 1
  start-page: 185
  year: 1993
  ident: D4RA05758A/cit22/1
  publication-title: Nat. Toxins
  doi: 10.1002/nt.2620010306
  contributor:
    fullname: Petrini
– volume: 16
  start-page: 1997
  year: 2018
  ident: D4RA05758A/cit74/1
  publication-title: Plant Biotechnol. J.
  doi: 10.1111/pbi.12933
  contributor:
    fullname: Delatte
– volume: 486
  start-page: 19
  year: 2000
  ident: D4RA05758A/cit50/1
  publication-title: FEBS Lett.
  doi: 10.1016/S0014-5793(00)02234-1
  contributor:
    fullname: Bailly
– volume: 123
  start-page: 155207
  year: 2024
  ident: D4RA05758A/cit5/1
  publication-title: Phytomedicine
  doi: 10.1016/j.phymed.2023.155207
  contributor:
    fullname: Sidhu
– volume: 10
  start-page: 18792
  year: 2020
  ident: D4RA05758A/cit19/1
  publication-title: Sci. Rep.
  doi: 10.1038/s41598-020-75722-1
  contributor:
    fullname: Kaur
– volume: 58
  start-page: 237
  year: 1990
  ident: D4RA05758A/cit44/1
  publication-title: Int. J. Pharm.
  doi: 10.1016/0378-5173(90)90201-E
  contributor:
    fullname: Kunchandy
– volume-title: The Quantitative Analysis of Drugs
  year: 2012
  ident: D4RA05758A/cit49/1
  contributor:
    fullname: Garratt
– volume: 13
  start-page: 872034
  year: 2022
  ident: D4RA05758A/cit53/1
  publication-title: Front. Microbiol.
  doi: 10.3389/fmicb.2022.872034
  contributor:
    fullname: Lin
– volume: 13
  start-page: 896421
  year: 2022
  ident: D4RA05758A/cit77/1
  publication-title: Front. Plant Sci.
  doi: 10.3389/fpls.2022.896421
  contributor:
    fullname: Chen
– volume: 35
  start-page: 365
  year: 2013
  ident: D4RA05758A/cit43/1
  publication-title: Immunopharmacol. Immunotoxicol.
  doi: 10.3109/08923973.2013.775588
  contributor:
    fullname: Roy
– volume: 20
  start-page: 265
  year: 2014
  ident: D4RA05758A/cit91/1
  publication-title: J. Neurogastroenterol. Motil.
  doi: 10.5056/jnm.2014.20.2.265
  contributor:
    fullname: Lee
– volume: 10
  start-page: 853
  year: 2019
  ident: D4RA05758A/cit75/1
  publication-title: Nat. Commun.
  doi: 10.1038/s41467-019-08515-4
  contributor:
    fullname: Sadre
– volume: 13
  start-page: 877
  year: 2015
  ident: D4RA05758A/cit14/1
  publication-title: Appl. Ecol. Environ. Res.
  contributor:
    fullname: Nath
– volume: 24
  start-page: 2739
  issue: 3
  year: 2023
  ident: D4RA05758A/cit89/1
  publication-title: Int. J. Mol. Sci.
  doi: 10.3390/ijms24032739
  contributor:
    fullname: Murotomi
– volume: 12
  start-page: 2094
  year: 2022
  ident: D4RA05758A/cit25/1
  publication-title: Sci. Rep.
  doi: 10.1038/s41598-022-05820-9
  contributor:
    fullname: Ezeonuegbu
– volume: 9
  start-page: 2370
  year: 2019
  ident: D4RA05758A/cit82/1
  publication-title: Sci. Rep.
  doi: 10.1038/s41598-019-38837-8
  contributor:
    fullname: Deng
– volume: 262
  start-page: 605
  year: 1999
  ident: D4RA05758A/cit46/1
  publication-title: Biochem. Biophys. Res. Commun.
  doi: 10.1006/bbrc.1999.1263
  contributor:
    fullname: Long
– volume: 41
  start-page: 249
  year: 2021
  ident: D4RA05758A/cit71/1
  publication-title: Crit. Rev. Biotechnol.
  doi: 10.1080/07388551.2020.1869691
  contributor:
    fullname: Yao
– volume: 9
  start-page: e21392
  issue: 11
  year: 2023
  ident: D4RA05758A/cit40/1
  publication-title: Heliyon
  doi: 10.1016/j.heliyon.2023.e21392
  contributor:
    fullname: Gandhi
– volume: 248
  start-page: 973
  year: 1987
  ident: D4RA05758A/cit51/1
  publication-title: Biochem. J.
  doi: 10.1042/bj2480973
  contributor:
    fullname: Aruoma
– volume: 13
  start-page: 19780
  year: 2023
  ident: D4RA05758A/cit83/1
  publication-title: Sci. Rep.
  doi: 10.1038/s41598-023-47260-z
  contributor:
    fullname: Qi
– volume: 74
  start-page: 4985
  year: 2008
  ident: D4RA05758A/cit92/1
  publication-title: Appl. Environ. Microbiol.
  doi: 10.1128/AEM.00753-08
  contributor:
    fullname: Walter
– volume: 26
  start-page: 6052
  year: 2021
  ident: D4RA05758A/cit37/1
  publication-title: Molecules
  doi: 10.3390/molecules26196052
  contributor:
    fullname: Wangkarn
– volume: 26
  start-page: 654
  issue: 3
  year: 2021
  ident: D4RA05758A/cit18/1
  publication-title: Molecules
  doi: 10.3390/molecules26030654
  contributor:
    fullname: Mani
– volume: 14
  start-page: 181
  year: 2016
  ident: D4RA05758A/cit27/1
  publication-title: J. Genet. Eng. Biotechnol.
  doi: 10.1016/j.jgeb.2015.12.003
  contributor:
    fullname: Rabha
– volume: 16
  start-page: 677
  year: 2018
  ident: D4RA05758A/cit55/1
  publication-title: Appl. Ecol. Environ. Res.
  doi: 10.15666/aeer/1601_677695
  contributor:
    fullname: Win
– volume: 6
  start-page: 7
  year: 2020
  ident: D4RA05758A/cit86/1
  publication-title: ChemTexts
  doi: 10.1007/s40828-019-0101-8
  contributor:
    fullname: Winterbourn
– volume: 9
  start-page: e109126
  year: 2014
  ident: D4RA05758A/cit12/1
  publication-title: PLoS One
  doi: 10.1371/journal.pone.0109126
  contributor:
    fullname: Ahmed
– volume: 58
  start-page: 2943
  year: 2019
  ident: D4RA05758A/cit93/1
  publication-title: Eur. J. Nutr.
  doi: 10.1007/s00394-018-01890-6
  contributor:
    fullname: Sharma
– volume: 84
  start-page: 108455
  year: 2020
  ident: D4RA05758A/cit35/1
  publication-title: J. Nutr. Biochem.
  doi: 10.1016/j.jnutbio.2020.108455
  contributor:
    fullname: Dey
– volume: 49
  start-page: 523
  year: 2013
  ident: D4RA05758A/cit17/1
  publication-title: Chem. Nat. Compd.
  doi: 10.1007/s10600-013-0658-1
  contributor:
    fullname: Cheng
– volume: 11
  start-page: 390
  year: 2020
  ident: D4RA05758A/cit72/1
  publication-title: Front. Plant Sci.
  doi: 10.3389/fpls.2020.00390
  contributor:
    fullname: He
– start-page: 237
  year: 2019
  ident: D4RA05758A/cit1/1
  publication-title: New Future Dev. Microb. Biotechnol. Bioeng.
  contributor:
    fullname: Vasundhara
– volume: 11
  start-page: 1001
  year: 2020
  ident: D4RA05758A/cit68/1
  publication-title: Bioengineered
  doi: 10.1080/21655979.2020.1816788
  contributor:
    fullname: Xie
– volume: 40
  start-page: W127
  year: 2012
  ident: D4RA05758A/cit41/1
  publication-title: Nucleic Acids Res.
  doi: 10.1093/nar/gks374
  contributor:
    fullname: Xia
– volume: 99
  start-page: 153
  year: 2014
  ident: D4RA05758A/cit65/1
  publication-title: Fitoterapia
  doi: 10.1016/j.fitote.2014.09.015
  contributor:
    fullname: Wang
– volume: 8
  start-page: 104
  issue: 1
  year: 2021
  ident: D4RA05758A/cit61/1
  publication-title: Hortic. Res.
  doi: 10.1038/s41438-021-00538-7
  contributor:
    fullname: Yu
– volume: 5
  start-page: 46
  year: 2017
  ident: D4RA05758A/cit8/1
  publication-title: Climate
  doi: 10.3390/cli5030046
  contributor:
    fullname: Marx
– volume: 18
  start-page: 6
  year: 2023
  ident: D4RA05758A/cit63/1
  publication-title: Res. J. Biotechnol.
  contributor:
    fullname: Ratul
– volume: 2014
  start-page: 792789
  year: 2014
  ident: D4RA05758A/cit4/1
  publication-title: Evid.-Based Complementary Altern. Med.
  doi: 10.1155/2014/792789
  contributor:
    fullname: Kunwar
– volume: 9
  start-page: 1191
  year: 2023
  ident: D4RA05758A/cit13/1
  publication-title: J. Fungi
  doi: 10.3390/jof9121191
  contributor:
    fullname: Onlamun
– volume: 130
  start-page: 70
  year: 2024
  ident: D4RA05758A/cit64/1
  publication-title: Arch. Physiol. Biochem.
  doi: 10.1080/13813455.2021.1966475
  contributor:
    fullname: Saha
– volume: 11
  start-page: 562785
  year: 2020
  ident: D4RA05758A/cit76/1
  publication-title: Front. Plant Sci.
  doi: 10.3389/fpls.2020.562785
  contributor:
    fullname: He
– volume: 83
  start-page: 57
  year: 2014
  ident: D4RA05758A/cit62/1
  publication-title: Phyton
  doi: 10.32604/phyton.2014.83.057
  contributor:
    fullname: Xj
– volume: 7
  start-page: 866
  year: 2017
  ident: D4RA05758A/cit57/1
  publication-title: Sci. Rep.
  doi: 10.1038/s41598-017-00972-5
  contributor:
    fullname: Liu
– volume: 13
  start-page: 20365
  year: 2023
  ident: D4RA05758A/cit78/1
  publication-title: Sci. Rep.
  doi: 10.1038/s41598-023-47657-w
  contributor:
    fullname: Han
– volume: 60
  start-page: 143
  year: 2010
  ident: D4RA05758A/cit33/1
  publication-title: Ann. Microbiol.
  doi: 10.1007/s13213-010-0016-5
  contributor:
    fullname: Qiu
– volume: 151
  start-page: 109768
  year: 2024
  ident: D4RA05758A/cit94/1
  publication-title: Food Hydrocolloids
  doi: 10.1016/j.foodhyd.2024.109768
  contributor:
    fullname: Xie
– volume: 12
  start-page: 930
  year: 2023
  ident: D4RA05758A/cit39/1
  publication-title: Antioxidants
  doi: 10.3390/antiox12040930
  contributor:
    fullname: Rezgui
– start-page: 15
  volume-title: Lipid Biotechnology
  year: 2002
  ident: D4RA05758A/cit73/1
  contributor:
    fullname: Schultz
– volume: 2
  start-page: 256
  year: 2022
  ident: D4RA05758A/cit87/1
  publication-title: Stresses
  doi: 10.3390/stresses2030019
  contributor:
    fullname: Andrés
– volume: 12
  start-page: 86
  year: 2022
  ident: D4RA05758A/cit2/1
  publication-title: 3 Biotech
  doi: 10.1007/s13205-022-03145-y
  contributor:
    fullname: Bhadra
– volume: 1
  start-page: 2320
  year: 2006
  ident: D4RA05758A/cit26/1
  publication-title: Nat. Protoc.
  doi: 10.1038/nprot.2006.384
  contributor:
    fullname: Allen
– volume: 17
  start-page: 519
  year: 2009
  ident: D4RA05758A/cit52/1
  publication-title: J. Rapid Methods Autom. Microbiol.
  doi: 10.1111/j.1745-4581.2009.00187.x
  contributor:
    fullname: Sultanbawa
SSID ssj0000651261
Score 2.4634979
Snippet Endophytes acquire flavonoid biosynthetic genes from the host medicinal plants. Despite tea ( (L.) Kuntze) being the major source of bioactive catechins,...
Endophytes acquire flavonoid biosynthetic genes from the host medicinal plants. Despite tea ( Camellia sinensis (L.) Kuntze) being the major source of...
Endophytes acquire flavonoid biosynthetic genes from the host medicinal plants. Despite tea (Camellia sinensis (L.) Kuntze) being the major source of bioactive...
Endophytes acquire flavonoid biosynthetic genes from the host medicinal plants. Despite tea ( Camellia sinensis (L.) Kuntze) being the major source of...
SourceID pubmedcentral
proquest
crossref
pubmed
SourceType Open Access Repository
Aggregation Database
Index Database
StartPage 33034
SubjectTerms Biochemistry
Biological activity
Biosynthesis
Catechin
Chemistry
Chromatography
Fatty acids
Fungi
Herbal medicine
High performance liquid chromatography
Metabolism
Plant layout
Tea
Title Chemical characterization, pathway enrichments and bioactive potentials of catechin-producing endophytic fungi isolated from tea leaves
URI https://www.ncbi.nlm.nih.gov/pubmed/39434990
https://www.proquest.com/docview/3124469973
https://www.proquest.com/docview/3119193724
https://pubmed.ncbi.nlm.nih.gov/PMC11492194
Volume 14
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://sdu.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1NT9wwEB11ubSXqt8NUOSqPTZsEseJfVwtIC6gqh9Sb9E4dkokSFbsbhG_gL_dGWezAnrr2Y4ceZ49b-SZNwCfrSYeUEuMlWxMnGOiYut8FucpBURpmaom6Gyffi_Pf-mjY5bJKcZamJC0X9v2sLu8Ouzai5Bbubiqp2Oe2PTr2Zw4vKGTlk8nMCFyeC9GH-5fcmJFOmqRSjN1-TUyL9GPvM8_lPJxZuQ9V3PyAp5vOKKYDf_yEp747hU8nY-t2V7D3VjmL-qt3vJQTvlFcIvhG7wVhIu2vggFbAI7J2zbY7jbxKJfcYoQ4U70jeCMKM6njBdB-5U8GX3qetp9Wl2Q2_vdipYAStOc4GIUQbAQlx7_-OUb-Hly_GN-Gm86KsQ1xS2ruGxYjosYjEoSj1jaJpGyVgYzm6EviswXBj2yKqByurYmdxYz7zR3qioVyrew0_Wdfw8i1U2DViXWZy4nTmAapYks-ERp1gAsIvg07nS1GIQzqvDgLU11lH-bBXvMItgfjVBtDs-yksw5CmNKGcHH7TBtMb9lYOf7Nc-hQJOoVZZH8G6w2XYZyZp35GUj0A-suZ3AktoPRwhpQVp7RNbu_3-6B88yIj7s39JyH3ZW12v_ASZLtz4IAf9BQOtfJWX0bQ
link.rule.ids 230,315,729,782,786,866,887,27933,27934,53800,53802
linkProvider National Library of Medicine
linkToHtml http://sdu.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1NT9wwEB0BPdBLS1vapnzUVTkSNonjxD6uFtCiAqoKlXqLxrFTIkGyYndb9Rf0bzN2Nis-bpxty1He2PNGnnkDsKcl8YCSYyh4pcIUIxFqY5MwjSkgivNYVF5ne3yRn_-Sh0dOJifra2F80n6p64Pm-uagqa98buXkphz0eWKD72cj4vCKTlo6WIUXdGCj6F6U3t3A5MayuFcj5Wpg0lt0zEQ-8j9PSOXj3Mh7zub49XM_cwNeLeglG3bjb2DFNm9hfdR3dXsH_3uFAFYupZq7Ssx95roT_8V_jEyqLq987RvDxjBdt-ivRTZpZy67iEyWtRVzyVQuFTOceNlYcoK01LQEHO3OyGP-rllNtk3TDHN1LIwsil1b_GOnm_Dz-OhyNA4XzRjCkkKeWZhXTsmLyI-IIouY6yrivBQKE52gzbLEZgotOkFBYWSpVWo0JtZI1-QqF8jfw1rTNvYjsFhWFWoRaZuYlOiEqoQknmEjIZ18YBbA1x6iYtJpbhT-rZyr4jD9MfRADgPY7tErFuduWnBHVzKlch7Al-Uw_WL3DIKNbeduDsWoxMqSNIAPHdjLbbiTyyMHHYB8YAbLCU6N--EIoe9VuXu0Pz1_6WdYH1-enRanJ-fftuBlQvzJuck434a12e3c7sDq1Mx3vbHfAb7TCT8
linkToPdf http://sdu.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV1Lb9QwEB7RIgGX8iwEChjBkTSJHSc2t9VuV0VAVfGQuEV2bNNIbRJ1d4v4Bfxtxs5m1ZYbnD2Wo8yM5xt55huAN1ogDqiZijlzMs5VymNtLI3zDBOirMy4Czzbh1_Ko-9iduBpct6NvTChaL_WzX57erbfNiehtrI_q5OxTiw5_jRFDC_R0_KkNy7ZgpvotCm9lKkPtzCGsiIbGUmZTEx-rjw6Eddi0F_A8np95KWAM7_7P596D3bWMJNMBpn7cMO2D-D2dJzu9hB-j0wBpN5QNg8dmW-Jn1L8U_0iaFpNfRJ64IhqDdFNp8L1SPpu6auM0HRJ54gvqvIlmXEf6GMxGOJW06EC8XSCkfNHQxq0cRQzxPezELQscmrVhV08gm_zg6_Tw3g9lCGuMfVZxqXzjF4IgniaWqVK7VLGai4V1VTZoqC2kMoqTyzIjai1zI1W1Brhh12VXLFd2G671j4BkgnnlOapttTkCCuk4wLxhk258DSCRQSvRzVV_cC9UYU3cyarWf55EpQ5iWBv1GC19r9FxTxsKaQsWQSvNsv4i_1ziGptt_IymKsiOqN5BI8HhW-OYZ42DwN1BOKKKWwEPCv31RW0gMDOPWr86b9vfQm3jmfz6uP7ow_P4A5FGOWjZVbuwfbyfGWfw9bCrF4Ee_8D9i4Lvw
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Chemical+characterization%2C+pathway+enrichments+and+bioactive+potentials+of+catechin-producing+endophytic+fungi+isolated+from+tea+leaves&rft.jtitle=RSC+advances&rft.au=Sidhu%2C+Dwinder&rft.au=Vasundhara%2C+M&rft.au=Dey%2C+Priyankar&rft.date=2024-10-17&rft.issn=2046-2069&rft.eissn=2046-2069&rft.volume=14&rft.issue=45&rft.spage=33034&rft_id=info:doi/10.1039%2Fd4ra05758a&rft.externalDBID=NO_FULL_TEXT
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=2046-2069&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=2046-2069&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=2046-2069&client=summon