Contents

Steroid 11β-hydroxylase

CYP11B1
Identifiers
Aliases	CYP11B1, CPN1, CYP11B, FHI, P450C11, cytochrome P450 family 11 subfamily B member 1
External IDs	OMIM: 610613; MGI: 88584; HomoloGene: 128035; GeneCards: CYP11B1; OMA:CYP11B1 - orthologs
EC number	1.14.15.4
Gene location (Human) Chr. Chromosome 8 (human)[1] Band 8q24.3 Start 142,872,356 bp[1] End 142,879,846 bp[1]
Gene location (Mouse) Chr. Chromosome 15 (mouse)[2] Band 15 D3|15 34.29 cM Start 74,722,859 bp[2] End 74,728,167 bp[2]
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in right adrenal cortex left adrenal gland left adrenal cortex testicle pancreatic ductal cell right testis right coronary artery left testis metanephros ectocervix Top expressed in adrenal gland lumbar subsegment of spinal cord lumbar spinal ganglion vastus lateralis muscle spermatid carotid body gastrula thoracic diaphragm triceps brachii muscle sternocleidomastoid muscle More reference expression data BioGPS More reference expression data
Gene ontology Molecular function iron ion binding corticosterone 18-monooxygenase activity metal ion binding monooxygenase activity oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen oxidoreductase activity steroid 11-beta-monooxygenase activity heme binding Cellular component membrane mitochondrial membranes mitochondrion mitochondrial inner membrane Biological process glucose homeostasis lipid metabolism aldosterone biosynthetic process cortisol biosynthetic process regulation of blood pressure C21-steroid hormone biosynthetic process cellular response to hormone stimulus glucocorticoid biosynthetic process immune response sterol metabolic process cellular response to potassium ion steroid biosynthetic process steroid metabolic process cholesterol metabolic process cellular response to peptide hormone stimulus cortisol metabolic process Sources:Amigo / QuickGO
Orthologs Species Human Mouse Entrez 1584 13072 Ensembl ENSG00000160882 ENSMUSG00000022589 UniProt P15538 P15539 RefSeq (mRNA) NM_000497 NM_001026213 NM_009991 RefSeq (protein) NP_000488 NP_001021384 NP_034121 Location (UCSC) Chr 8: 142.87 – 142.88 Mb Chr 15: 74.72 – 74.73 Mb PubMed search [3] [4]
Wikidata
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Steroid 11β-hydroxylase, also known as steroid 11β-monooxygenase, is a steroid hydroxylase found in the zona glomerulosa and zona fasciculata of the adrenal cortex. Named officially the cytochrome P450 11B1, mitochondrial, it is a protein that in humans is encoded by the CYP11B1 gene.^[5][6] The enzyme is involved in the biosynthesis of adrenal corticosteroids^[7] by catalyzing the addition of hydroxyl groups during oxidation reactions.

The CYP11B1 gene encodes 11β-hydroxylase, a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases that catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. The product of this CYP11B1 gene is the 11β-hydroxylase protein. This protein localizes to the mitochondrial inner membrane and is involved in the conversion of various steroids in the adrenal cortex. Transcript variants encoding different isoforms have been noted for this gene.^[6]

The CYP11B1 gene is reversibly inhibited by etomidate^[8][9] and metyrapone.

11β-hydroxylase is a steroidogenic enzyme, i.e. the enzyme involved in the metabolismofsteroids. The enzyme is primarily localized in the zona glomerulosa and zona fasciculata of the adrenal cortex. The enzyme functions by introducing a hydroxyl group at carbon position 11β on the steroid nucleus, thereby facilitating the conversion of certain steroids.

Humans have two isozymes with 11β-hydroxylase activity: CYP11B1 and CYP11B2.

CYP11B1 (11β-hydroxylase) is expressed at high levels and is regulated by ACTH, while CYP11B2 (aldosterone synthase) is usually expressed at low levels and is regulated by angiotensin II. In addition to the 11β-hydroxylase activity, both isozymes have 18-hydroxylase activity.^[10] The CYP11B1 isozyme has strong 11β-hydroxylase activity, but the activity of 18-hydroxylase is only one-tenth of CYP11B2.^[11] The weak 18-hydroxylase activity of CYP11B1 explains why an adrenal with suppressed CYP11B2 expression continues to synthesize 18-hydroxycorticosterone.^[12]

Here are some of the steroids, grouped by catalytic activity of the CYP11B1 isozyme:

• strong activity:^[13][14]
  • 11-deoxycortisoltocortisol,^[12][15]
  • 11-deoxycorticosteronetocorticosterone;^[12][16]
• medium activity:^[13][14]
  • progesteroneto11β-hydroxyprogesterone,^[14][17][18]
  • 17α-hydroxyprogesteroneto21-deoxycortisol,^[17]
  • androstenedioneto11β-hydroxyandrostenedione;^[19]
  • testosteroneto11β-hydroxytestosterone,^[20][21][14]
• weak activity:^[13][14]
  • corticosteroneto18-hydroxycorticosterone,^[12][22]
  • cortisolto18-hydroxycortisol.^{[13][22][23][24]}

11β-hydroxylase has strong^[13] catalytic activity during conversion of 11-deoxycortisoltocortisol and 11-deoxycorticosteronetocorticosterone, by catalyzing the hydroxylation of carbon hydrogen bond at 11-beta position. Note the extra『–OH』added at the 11 position (near the center, on ring "C"):

• 
  11-Deoxycortisol
• 
  Cortisol

• 
  11-Deoxycorticosterone
• 
  Corticosterone

As a mitochondrial P450 system, P450c11 is dependent on two electron transfer proteins, adrenodoxin reductase and adrenodoxin that transfer 2 electrons from NADPH to the P450 for each monooxygenase reaction catalyzed by the enzyme. In most respects this process of electron transfer appears similar to that of P450scc system that catalyzes cholesterol side chain cleavage.^[25] Similar to P450scc the process of electrons transfer is leaky leading to superoxide production. The rate of electron leakage during metabolism depends on the functional groups of the steroid substrate.^[26]

The expression of the enzyme in adrenocortical cells is regulated by the trophic hormone corticotropin (ACTH).^[27]

A mutation in genes encoding 11β-hydroxylase is associated with congenital adrenal hyperplasia due to 11β-hydroxylase deficiency.

11β-hydroxylase is involved in the metabolism of 17α-hydroxyprogesteroneto21-deoxycortisol,^[17] in cases of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.^[28][29]

• Steroidogenic enzyme

• 
  Corticosteroid biosynthetic pathway in rat
• 
  Steroid numbering

^ ^{a b}  This article incorporates public domain material from "Entrez Gene: CYP11B1 cytochrome P450, family 11, subfamily B, polypeptide 1". Reference Sequence collection. National Center for Biotechnology Information. Retrieved 30 November 2020. This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This protein localizes to the mitochondrial inner membrane and is involved in the conversion of progesterone to cortisol in the adrenal cortex. Mutations in this gene cause congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency. Transcript variants encoding different isoforms have been noted for this gene. This article incorporates text from this source, which is in the public domain.

^ Masiutin MM, Yadav MK (3 April 2023). "Alternative androgen pathways" (PDF). WikiJournal of Medicine. 10: 29. doi:10.15347/WJM/2023.003. S2CID 257943362. This article incorporates text from this source, which is available under the CC BY 4.0 license.

• Steroid+11-beta-hydroxylase at the U.S. National Library of Medicine Medical Subject Headings (MeSH)